@article{doi:10.1021/acs.accounts.2c00525,
author = {Reuss, Torben and Nair Lalithambika, Sreeju Sreekantan and David, Christian and Döring, Florian and Jooss, Christian and Risch, Marcel and Techert, Simone},
title = {Advancements in Liquid Jet Technology and X-ray Spectroscopy for Understanding Energy Conversion Materials during Operation},
journal = {Accounts of Chemical Research},
volume = {56},
number = {3},
pages = {203-214},
year = {2023},
doi = {10.1021/acs.accounts.2c00525},
    note ={PMID: 36636991},
URL = {https://doi.org/10.1021/acs.accounts.2c00525},
eprint = {https://doi.org/10.1021/acs.accounts.2c00525}

}

@misc{rajpurohit2023characteristic,
      title={Characteristic THz-emissions induced by optically excited collective orbital modes}, 
      author={Sangeeta Rajpurohit and Christian Jooss and Simone Techert and Tadashi Ogitsu and P. E. Blöchl and L. Z. Tan},
      year={2023},
      eprint={2306.09107},
      archivePrefix={arXiv},
      primaryClass={cond-mat.str-el}
}

@misc{lindner2023reconstruction,
      title={Reconstruction of {\AA}ngstr{\o}m resolution exit-waves by the application of drift-corrected phase-shifting off-axis electron holography}, 
      author={J. Lindner and U. Ross and T. Meyer and M. Seibt and Ch. Jooss},
      year={2023},
      eprint={2303.16054},
      archivePrefix={arXiv},
      primaryClass={cond-mat.mtrl-sci}
}

@article{10.1016/j.jcrysgro.2022.126972,
doi = {10.1016/j.jcrysgro.2022.126972},
url = {http://dx.doi.org/10.1016/j.jcrysgro.2022.126972},
year = 2023,
publisher = {Elsevier {BV}},
volume = {602},
pages = {126972},
author = {Tobias Niemeyer and Kevin Meyer and Christoph Flathmann and Tobias Meyer and Daniel M. Schaadt and Michael Seibt},
title = {Microstructural analysis of {GaN} films grown on (1 0 0) {MgF}2 substrate by 4D nanobeam diffraction and energy-dispersive X-ray spectrometry},
journal = {Journal of Crystal Growth}
}

@article{10.1021/acs.jpcc.2c05622,
doi = {10.1021/acs.jpcc.2c05622},
url = {http://dx.doi.org/10.1021/acs.jpcc.2c05622},
year = 2023,
publisher = {American Chemical Society ({ACS})},
volume = {127},
pages = {177--186},
author = {Gaurav Lole and Fatemeh Ebrahimi and Tobias Meyer and Daniel Mierwaldt and Vladimir Roddatis and Janis Geppert and Marcel Risch and Christian Jooss},
title = {Contrasting Pr1-xCaxMnO3 OER Catalyst with Different Valence and Covalence},
journal = {The Journal of Physical Chemistry C}
}

@article{10.1016/j.ultramic.2022.113629,
doi = {10.1016/j.ultramic.2022.113629},
url = {http://dx.doi.org/10.1016/j.ultramic.2022.113629},
year = 2023,
publisher = {Elsevier {BV}},
volume = {243},
pages = {113629},
author = {J. Lindner and U. Ross and V. Roddatis and Ch. Jooss},
title = {Langmuir analysis of electron beam induced plasma in environmental {Tem}},
journal = {Ultramicroscopy}
}

@article{10.1246/bcsj.20210323,
doi = {10.1246/bcsj.20210323},
url = {http://dx.doi.org/10.1246/bcsj.20210323},
year = 2022,
publisher = {The Chemical Society of Japan},
volume = {95},
pages = {73--103},
author = {Andrew Chapman and Elif Ertekin and Masanobu Kubota and Akihide Nagao and Kaila Bertsch and Arnaud Macadre and Toshihiro Tsuchiyama and Takuro Masamura and Setsuo Takaki and Ryosuke Komoda and Mohsen Dadfarnia and Brian 
Somerday and Alexander Tsekov Staykov and Joichi Sugimura and Yoshinori Sawae and Takehiro Morita and Hiroyoshi Tanaka and Kazuyuki Yagi and Vlad Niste and Prabakaran Saravanan and Shugo Onitsuka and Ki-Seok Yoon and Seiji Ogo 
and Toshinori Matsushima and Ganbaatar Tumen-Ulzii and Dino Klotz and Dinh Hoa Nguyen and George Harrington and Chihaya Adachi and Hiroshige Matsumoto and Leonard Kwati and Yukina Takahashi and Nuttavut Kosem and Tatsumi Ishihara 
and Miho Yamauchi and Bidyut Baran Saha and Md. Amirul Islam and Jin Miyawaki and Harish Sivasankaran and Masamichi Kohno and Shigenori Fujikawa and Roman Selyanchyn and Takeshi Tsuji and Yukihiro Higashi and Reiner Kirchheim and 
Petros Sofronis},
title = {Achieving a Carbon Neutral Future through Advanced Functional Materials and Technologies},
journal = {Bulletin of the Chemical Society of Japan}
}

@article{10.1016/j.actamat.2021.117474,
doi = {10.1016/j.actamat.2021.117474},
url = {http://dx.doi.org/10.1016/j.actamat.2021.117474},
year = 2022,
publisher = {Elsevier {BV}},
volume = {223},
pages = {117474},
author = {Lin Tian and Christine Borchers and Masanobu Kubota and Petros Sofronis and Reiner Kirchheim and Cynthia A. Volkert},
title = {A study of crack initiation in a low alloy steel},
journal = {Acta Materialia}
}

@article{10.1021/acs.jchemed.1c01157,
doi = {10.1021/acs.jchemed.1c01157},
url = {http://dx.doi.org/10.1021/acs.jchemed.1c01157},
year = 2022,
publisher = {American Chemical Society ({ACS})},
volume = {99},
pages = {2086--2092},
author = {Mona Christin Maa{\ss} and Alexander Tasch and Christian Jooss and Thomas Waitz},
title = {Photocatalytic Hydrogen Evolution Using {ZnS} Particles and {Leds}},
journal = {Journal of Chemical Education}
}

@article{10.1007/s00425-022-03976-2,
doi = {10.1007/s00425-022-03976-2},
url = {http://dx.doi.org/10.1007/s00425-022-03976-2},
year = 2022,
publisher = {Springer Science and Business Media {LLC}},
volume = {256},
author = {Mona C. Maa{\ss} and Salimeh Saleh and Holger Militz and Cynthia A. Volkert},
title = {Radial microfibril arrangements in wood cell walls},
journal = {Planta}
}

@article{10.3390/met12030489,
doi = {10.3390/met12030489},
url = {http://dx.doi.org/10.3390/met12030489},
year = 2022,
publisher = {{MDPI} {AG}},
volume = {12},
pages = {489},
author = {Shyamal Roy and Sönke Wille and Dan Mordehai and Cynthia A. Volkert},
title = {Investigating Nanoscale Contact Using {Afm}-Based Indentation and Molecular Dynamics Simulations},
journal = {Metals}
}

@article{10.1002/anie.202211949,
doi = {10.1002/anie.202211949},
url = {http://dx.doi.org/10.1002/anie.202211949},
year = 2022,
publisher = {Wiley},
volume = {61},
author = {Marcel Risch and Dulce M. Morales and Javier Villalobos and Denis Antipin},
title = {What X-Ray Absorption Spectroscopy Can Tell Us About the Active State of Earth-Abundant Electrocatalysts for the Oxygen Evolution Reaction{\ast}{\ast}},
journal = {Angewandte Chemie International Edition}
}

@article{10.1364/oe.471111,
doi = {10.1364/oe.471111},
url = {http://dx.doi.org/10.1364/oe.471111},
year = 2022,
publisher = {Optica Publishing Group},
volume = {30},
pages = {47744},
author = {Steffen Bornemann and Tobias Meyer and Tobias Voss and Andreas Waag},
title = {Ablation threshold of {GaN} films for ultrashort laser pulses and the role of threading dislocations as damage precursors},
journal = {Optics Express}
}

@article{10.1021/jacs.2c07226,
doi = {10.1021/jacs.2c07226},
url = {http://dx.doi.org/10.1021/jacs.2c07226},
year = 2022,
publisher = {American Chemical Society ({ACS})},
volume = {144},
pages = {17966--17979},
author = {Moritz L. Weber and Gaurav Lole and Attila Kormanyos and Alexander Schwiers and Lisa Heymann and Florian D. Speck and Tobias Meyer and Regina Dittmann and Serhiy Cherevko and Christian Jooss and Christoph Baeumer and Felix Gunkel},
title = {Atomistic Insights into Activation and Degradation of La0.6Sr0.4CoO3−δ Electrocatalysts under Oxygen Evolution Conditions},
journal = {Journal of the American Chemical Society}
}

@misc{10.48550/arxiv.2205.01151,
doi = {10.48550/ARXIV.2205.01151},
url = {http://dx.doi.org/10.48550/arxiv.2205.01151},
author = {Lee, Miru and Weber, Niklas and Volkert, Cynthia A. and Krüger, Matthias},
keywords = {Statistical Mechanics (cond-mat.stat-mech), Mesoscale and Nanoscale Physics (cond-mat.mes-hall), Materials Science (cond-mat.mtrl-sci), FOS: Physical sciences, FOS: Physical sciences},
title = {Friction on layered media: How deep do phonons reach?},
publisher = {arXiv},
year = {2022},
copyright = {arXiv.org perpetual, non-exclusive license}
}

@misc{10.48550/arxiv.2210.09677,
doi = {10.48550/ARXIV.2210.09677},
url = {http://dx.doi.org/10.48550/arxiv.2210.09677},
author = {Weber, Niklas A. and Lee, Miru and Schönewald, Florian and Schüler, Leonard and Moshnyaga, Vasily and Krüger, Matthias and Volkert, Cynthia A.},
keywords = {Materials Science (cond-mat.mtrl-sci), FOS: Physical sciences, FOS: Physical sciences},
title = {Nanoscale friction controlled by top layer thickness in [LaMnO$_{3}$]$_{m}$/[SrMnO$_{3}$]$_{n}$ superlattices},
publisher = {arXiv},
year = {2022},
copyright = {arXiv.org perpetual, non-exclusive license}
}

@article{doi:10.1021/jacs.2c07226,
author = {Weber, Moritz L. and Lole, Gaurav and Kormanyos, Attila and Schwiers, Alexander and Heymann, Lisa and Speck, Florian D. and Meyer, Tobias and Dittmann, Regina and Cherevko, Serhiy and Jooss, Christian and Baeumer, Christoph and Gunkel, Felix},
title = {Atomistic Insights into Activation and Degradation of La0.6Sr0.4CoO3−δ Electrocatalysts under Oxygen Evolution Conditions},
journal = {Journal of the American Chemical Society},
volume = {144},
number = {39},
pages = {17966-17979},
year = {2022},
doi = {10.1021/jacs.2c07226},
    note ={PMID: 36130265},
URL = {https://doi.org/10.1021/jacs.2c07226},
eprint = {https://doi.org/10.1021/jacs.2c07226}
}

@article{doi:10.1021/acs.jchemed.1c01157,
author = {Maaß, Mona Christin and Tasch, Alexander and Jooss, Christian and Waitz, Thomas},
title = {Photocatalytic Hydrogen Evolution Using ZnS Particles and LEDs},
journal = {Journal of Chemical Education},
volume = {99},
number = {5},
pages = {2086-2092},
year = {2022},
doi = {10.1021/acs.jchemed.1c01157},
URL = {https://doi.org/10.1021/acs.jchemed.1c01157},
eprint = {https://doi.org/10.1021/acs.jchemed.1c01157}
}

@article{https://doi.org/10.1002/zaac.202200119,
author = {Nestke, Sebastian and Stubbe, Jessica and Koehler, Robert and Ronge, Emanuel and Albold, Uta and Vioel, Wolfgang and Jooss, Christian and Sarkar, Biprajit and Siewert, Inke},
title = {A Binuclear Cobalt Complex in the Electrochemical Water Oxidation Reaction},
journal = {Zeitschrift für anorganische und allgemeine Chemie},
volume = {648},
number = {13},
pages = {e202200119},
keywords = {Cobalt, Coordination Chemistry, Electrocatalysis, N-Donor Ligands},
doi = {https://doi.org/10.1002/zaac.202200119},
url = {https://onlinelibrary.wiley.com/doi/abs/10.1002/zaac.202200119},
eprint = {https://onlinelibrary.wiley.com/doi/pdf/10.1002/zaac.202200119},
abstract = {Abstract The water splitting reaction represents an appealing approach to store solar energy. The 4e−/4H+ oxidation of water generating O2 is considered as the bottleneck in this reaction and usually requires a rather large over potential. We report on the synthesis and application of a binuclear cobalt(III) complex, 1, with two μ-OH ligands and tripodal triazole ligands, L, in the electrochemical water oxidation reaction (WOR; L=tris((1-phenyl-1H-1,2,3-triazol-4-yl)methyl)amine). The cobalt(III) centres in the complex exhibit an octahedral coordination geometry and the complex is stable in water. Electrochemical studies revealed that solutions of 1NO3 catalyse the WOR in phosphate or borate buffer. However, further analysis showed, that 1NO3 is a precursor and decomposes under the applied potential. A smooth deposit is formed on the electrode surface, which is a highly active water oxidation catalysis. The deposit consists of mainly cobalt oxide/hydroxide, which accounts for the catalytic activity, and small amounts of 1NO3.},
year = {2022}
}

Abstract The water splitting reaction represents an appealing approach to store solar energy. The 4e−/4H+ oxidation of water generating O2 is considered as the bottleneck in this reaction and usually requires a rather large over potential. We report on the synthesis and application of a binuclear cobalt(III) complex, 1, with two μ-OH ligands and tripodal triazole ligands, L, in the electrochemical water oxidation reaction (WOR; L=tris((1-phenyl-1H-1,2,3-triazol-4-yl)methyl)amine). The cobalt(III) centres in the complex exhibit an octahedral coordination geometry and the complex is stable in water. Electrochemical studies revealed that solutions of 1NO3 catalyse the WOR in phosphate or borate buffer. However, further analysis showed, that 1NO3 is a precursor and decomposes under the applied potential. A smooth deposit is formed on the electrode surface, which is a highly active water oxidation catalysis. The deposit consists of mainly cobalt oxide/hydroxide, which accounts for the catalytic activity, and small amounts of 1NO3.

@article{MEYER2021113320,
title = {Site-specific plan-view TEM lamella preparation of pristine surfaces with a large field of view},
journal = {Ultramicroscopy},
volume = {228},
pages = {113320},
year = {2021},
issn = {0304-3991},
doi = {https://doi.org/10.1016/j.ultramic.2021.113320},
url = {https://www.sciencedirect.com/science/article/pii/S0304399121001054},
author = {Tobias Meyer and Tobias Westphal and Birte Kressdorf and Ulrich Ross and Christian Jooss and Michael Seibt},
keywords = {TEM, Lamella, Preparation, Plan-view, Site-specific, Field of view},
abstract = {Transmission electron microscopy has become a major characterization tool with an ever increasing variety of methods being applied in a wide range of scientific fields. However, the probably most famous pitfall in related workflows is the preparation of high-quality electron-transparent lamellae enabling for extraction of valuable information. Particularly in the field of solid state physics and materials science, it often required to study the surface of a macroscopic specimen with plan-view orientation. Nevertheless, despite tremendous advances in instrumentation, i.e. focused ion beam, the yield of existing plan-view lamellae preparation techniques is relatively low compared to cross-sectional extraction methods. Furthermore, techniques relying on mechanical treatments, i.e. conventional preparation, compromise site-specifity. In this paper, we demonstrate that by combining a mechanical grinding step prior to backside lift-out in the focused ion beam plan-view lamellae preparation becomes increasingly easy. The suggested strategy combines site-specifity with micrometer precision as well as possible investigation of pristine surfaces with a field of view of several hundred square micrometers.}
}

Transmission electron microscopy has become a major characterization tool with an ever increasing variety of methods being applied in a wide range of scientific fields. However, the probably most famous pitfall in related workflows is the preparation of high-quality electron-transparent lamellae enabling for extraction of valuable information. Particularly in the field of solid state physics and materials science, it often required to study the surface of a macroscopic specimen with plan-view orientation. Nevertheless, despite tremendous advances in instrumentation, i.e. focused ion beam, the yield of existing plan-view lamellae preparation techniques is relatively low compared to cross-sectional extraction methods. Furthermore, techniques relying on mechanical treatments, i.e. conventional preparation, compromise site-specifity. In this paper, we demonstrate that by combining a mechanical grinding step prior to backside lift-out in the focused ion beam plan-view lamellae preparation becomes increasingly easy. The suggested strategy combines site-specifity with micrometer precision as well as possible investigation of pristine surfaces with a field of view of several hundred square micrometers.

@article{https://doi.org/10.1002/advs.202003524,
author = {Weber, Niklas A. and Schmidt, Hendrik and Sievert, Tim and Jooss, Christian and Güthoff, Friedrich and Moshneaga, Vasily and Samwer, Konrad and Krüger, Matthias and Volkert, Cynthia A.},
title = {Polaronic Contributions to Friction in a Manganite Thin Film},
journal = {Advanced Science},
volume = {8},
number = {8},
pages = {2003524},
keywords = {atomic force microscopy, friction, friction force microscopy, manganite, polarons},
doi = {https://doi.org/10.1002/advs.202003524},
url = {https://onlinelibrary.wiley.com/doi/abs/10.1002/advs.202003524},
eprint = {https://onlinelibrary.wiley.com/doi/pdf/10.1002/advs.202003524},
abstract = {Abstract Despite the huge importance of friction in regulating movement in all natural and technological processes, the mechanisms underlying dissipation at a sliding contact are still a matter of debate. Attempts to explain the dependence of measured frictional losses at nanoscale contacts on the electronic degrees of freedom of the surrounding materials have so far been controversial. Here, it is proposed that friction can be explained by considering the damping of stick-slip pulses in a sliding contact. Based on friction force microscopy studies of La(1−x)SrxMnO3 films at the ferromagnetic-metallic to a paramagnetic-polaronic conductor phase transition, it is confirmed that the sliding contact generates thermally-activated slip pulses in the nanoscale contact, and argued that these are damped by direct coupling into the phonon bath. Electron-phonon coupling leads to the formation of Jahn–Teller polarons and to a clear increase in friction in the high-temperature phase. There is neither evidence for direct electronic drag on the atomic force microscope tip nor any indication of contributions from electrostatic forces. This intuitive scenario, that friction is governed by the damping of surface vibrational excitations, provides a basis for reconciling controversies in literature studies as well as suggesting possible tactics for controlling friction.},
year = {2021}
}

Abstract Despite the huge importance of friction in regulating movement in all natural and technological processes, the mechanisms underlying dissipation at a sliding contact are still a matter of debate. Attempts to explain the dependence of measured frictional losses at nanoscale contacts on the electronic degrees of freedom of the surrounding materials have so far been controversial. Here, it is proposed that friction can be explained by considering the damping of stick-slip pulses in a sliding contact. Based on friction force microscopy studies of La(1−x)SrxMnO3 films at the ferromagnetic-metallic to a paramagnetic-polaronic conductor phase transition, it is confirmed that the sliding contact generates thermally-activated slip pulses in the nanoscale contact, and argued that these are damped by direct coupling into the phonon bath. Electron-phonon coupling leads to the formation of Jahn–Teller polarons and to a clear increase in friction in the high-temperature phase. There is neither evidence for direct electronic drag on the atomic force microscope tip nor any indication of contributions from electrostatic forces. This intuitive scenario, that friction is governed by the damping of surface vibrational excitations, provides a basis for reconciling controversies in literature studies as well as suggesting possible tactics for controlling friction.

@article{PhysRevB.104.195116,
  title = {Charge density wave breakdown in a heterostructure with electron-phonon coupling},
  author = {Jansen, David and Jooss, Christian and Heidrich-Meisner, Fabian},
  journal = {Phys. Rev. B},
  volume = {104},
  issue = {19},
  pages = {195116},
  numpages = {14},
  year = {2021},
  month = {Nov},
  publisher = {American Physical Society},
  doi = {10.1103/PhysRevB.104.195116},
  url = {https://link.aps.org/doi/10.1103/PhysRevB.104.195116}
}

@article{https://doi.org/10.1002/chem.202101894,
author = {Choi, Isaac and Shen, Zhigao and Ronge, Emanuel and Karius, Volker and Jooss, Christian and Ackermann, Lutz},
title = {Reusable Manganese Catalyst for Site-Selective Pyridine C−H Arylations and Alkylations},
journal = {Chemistry – A European Journal},
volume = {27},
number = {50},
pages = {12737-12741},
keywords = {C−H alkylation, C−H arylation, hybrid catalysis, manganese catalysis, site-selectivity},
doi = {https://doi.org/10.1002/chem.202101894},
url = {https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/chem.202101894},
eprint = {https://chemistry-europe.onlinelibrary.wiley.com/doi/pdf/10.1002/chem.202101894},
abstract = {Abstract Herein, we disclose a recyclable, hybrid manganese catalyst for site-selective azine C−H activation by weak amide assistance. The novel, reusable catalyst enabled C3–H arylation and C3–H alkylation with ample scope, and was characterized by detailed transmission electron microscopy analysis.},
year = {2021}
}

Abstract Herein, we disclose a recyclable, hybrid manganese catalyst for site-selective azine C−H activation by weak amide assistance. The novel, reusable catalyst enabled C3–H arylation and C3–H alkylation with ample scope, and was characterized by detailed transmission electron microscopy analysis.

@article{PhysRevB.103.235122,
  title = {Orbital-order phase transition in ${\mathrm{Pr}}_{1\ensuremath{-}x}{\mathrm{Ca}}_{x}{\mathrm{MnO}}_{3}$ probed by photovoltaics},
  author = {Kressdorf, B. and Meyer, T. and ten Brink, M. and Seick, C. and Melles, S. and Ottinger, N. and Titze, T. and Meer, H. and Weisser, A. and Hoffmann, J. and Mathias, S. and Ulrichs, H. and Steil, D. and Seibt, M. and Bl\"ochl, P. E. and Jooss, C.},
  journal = {Phys. Rev. B},
  volume = {103},
  issue = {23},
  pages = {235122},
  numpages = {21},
  year = {2021},
  month = {Jun},
  publisher = {American Physical Society},
  doi = {10.1103/PhysRevB.103.235122},
  url = {https://link.aps.org/doi/10.1103/PhysRevB.103.235122}
}

@article{https://doi.org/10.1002/admi.202002049,
author = {Hoffmann-Urlaub, Sarah and Ross, Ulrich and Hoffmann, Jörg and Belenchuk, Alexandr and Shapoval, Oleg and Roddatis, Vladimir and Ma, Qian and Kressdorf, Birte and Moshnyaga, Vasily and Jooss, Christian},
title = {Tailoring c-Axis Orientation in Epitaxial Ruddlesden–Popper Pr0.5Ca1.5MnO4 Films},
journal = {Advanced Materials Interfaces},
volume = {8},
number = {7},
pages = {2002049},
keywords = {epitaxy, Ruddlesden-Popper manganites, thin film growth},
doi = {https://doi.org/10.1002/admi.202002049},
url = {https://onlinelibrary.wiley.com/doi/abs/10.1002/admi.202002049},
eprint = {https://onlinelibrary.wiley.com/doi/pdf/10.1002/admi.202002049},
abstract = {Abstract Interest in layered Ruddlesden–Popper (RP) strongly correlated manganites of Pr0.5Ca1.5MnO4 as well as in their thin film polymorphs is motivated by the high temperature of charge orbital ordering above room temperature. The c-axis orientation in epitaxial films is tailored by different SrTiO3 (STO) substrate orientations and CaMnO3 (CMO) buffer layers. Films on STO(110) show in-plane alignment of the c-axis parallel to the [100] direction. On STO(100), two possible directions of the in-plane c-axis lead to a mosaic like, quasi 2D nanostructure, consisting of RP, rock-salt, and perovskite blocks. With the CMO buffer layer, Pr0.5Ca1.5MnO4 epitaxial films with c-axis out-of-plane are realized. Different physical vapor deposition techniques as ion beam sputtering, pulsed laser deposition and metalorganic aerosol deposition are applied in order to distinguish effects of growth conditions from intrinsic epitaxial properties. Despite their very different growth conditions, surface morphology, crystal structure, and orientation of the thin films reveal a high level of similarity as verified by X-ray diffraction, scanning, and high resolution transmission electron microscopy. For different epitaxial relations stress in the films is relaxed by means of modified interface chemistry. The charge ordering in the films occurs at a temperature close to that expected in bulk material.},
year = {2021}
}

Abstract Interest in layered Ruddlesden–Popper (RP) strongly correlated manganites of Pr0.5Ca1.5MnO4 as well as in their thin film polymorphs is motivated by the high temperature of charge orbital ordering above room temperature. The c-axis orientation in epitaxial films is tailored by different SrTiO3 (STO) substrate orientations and CaMnO3 (CMO) buffer layers. Films on STO(110) show in-plane alignment of the c-axis parallel to the [100] direction. On STO(100), two possible directions of the in-plane c-axis lead to a mosaic like, quasi 2D nanostructure, consisting of RP, rock-salt, and perovskite blocks. With the CMO buffer layer, Pr0.5Ca1.5MnO4 epitaxial films with c-axis out-of-plane are realized. Different physical vapor deposition techniques as ion beam sputtering, pulsed laser deposition and metalorganic aerosol deposition are applied in order to distinguish effects of growth conditions from intrinsic epitaxial properties. Despite their very different growth conditions, surface morphology, crystal structure, and orientation of the thin films reveal a high level of similarity as verified by X-ray diffraction, scanning, and high resolution transmission electron microscopy. For different epitaxial relations stress in the films is relaxed by means of modified interface chemistry. The charge ordering in the films occurs at a temperature close to that expected in bulk material.

@Article{D1SE01076J,
author ="Ronge, Emanuel and Ohms, Jonas and Roddatis, Vladimir and Jones, Travis and Sulzmann, Frederic and Knop-Gericke, Axel and Schlögl, Robert and Kurz, Philipp and Jooss, Christian and Skorupska, Katarzyna",
title  ="Operation of calcium-birnessite water-oxidation anodes: interactions of the catalyst with phosphate buffer anions",
journal  ="Sustainable Energy Fuels",
year  ="2021",
volume  ="5",
issue  ="21",
pages  ="5535-5547",
publisher  ="The Royal Society of Chemistry",
doi  ="10.1039/D1SE01076J",
url  ="http://dx.doi.org/10.1039/D1SE01076J",
abstract  ="Investigating the interfaces between electrolytes and electrocatalysts during electrochemical water oxidation is of great importance for an understanding of the factors influencing catalytic activity and stability. Here{,} the interaction of a well-established{,} nanocrystalline and mesoporous Ca-birnessite catalyst material (initial composition K0.2Ca0.21MnO2.21·1.4H2O{,} initial Mn-oxidation state ∼+3.8) with an aqueous potassium phosphate buffer electrolyte at pH 7 was studied mainly by using various electron microscopy and X-ray spectroscopy techniques. In comparison to electrolyte solutions not containing phosphate{,} the investigated Ca-birnessite electrodes show especially high and stable oxygen evolution activity in phosphate buffer. During electrolysis{,} partial ion substitutions of Ca2+ by K+ and OH−/O2− by HnPO4(3−n)− were observed{,} leading to the formation of a stable{,} partially disordered Ca–K–Mn–HnPO4–H2O layer on the outer and the pore surfaces of the active electrocatalyst material. In this surface layer{,} Mn3+ ions are stabilized{,} which are often assumed to be of key importance for oxygen evolution catalysis. Furthermore{,} evidence for the formation of [Ca/PO4/H2O]− complexes located between the [MnO6] layers of the birnessite was found using the soft Ca 2p and Ca L-edge X-ray spectroscopy. A possible way to interpret the observed{,} obviously very favorable “special relationship” between (hydrogen)phosphates and Ca-birnessites in electrocatalytic water oxidation would be that HnPO4(3−n)− anions are incorporated into the catalyst material where they act as stabilizing units for Mn3+ highly active centers and also as “internal bases” for the protons released during the water-oxidation reaction."
}

Investigating the interfaces between electrolytes and electrocatalysts during electrochemical water oxidation is of great importance for an understanding of the factors influencing catalytic activity and stability. Here, the interaction of a well-established, nanocrystalline and mesoporous Ca-birnessite catalyst material (initial composition K0.2Ca0.21MnO2.21·1.4H2O, initial Mn-oxidation state ∼+3.8) with an aqueous potassium phosphate buffer electrolyte at pH 7 was studied mainly by using various electron microscopy and X-ray spectroscopy techniques. In comparison to electrolyte solutions not containing phosphate, the investigated Ca-birnessite electrodes show especially high and stable oxygen evolution activity in phosphate buffer. During electrolysis, partial ion substitutions of Ca2+ by K+ and OH−/O2− by HnPO4(3−n)− were observed, leading to the formation of a stable, partially disordered Ca–K–Mn–HnPO4–H2O layer on the outer and the pore surfaces of the active electrocatalyst material. In this surface layer, Mn3+ ions are stabilized, which are often assumed to be of key importance for oxygen evolution catalysis. Furthermore, evidence for the formation of [Ca/PO4/H2O]− complexes located between the [MnO6] layers of the birnessite was found using the soft Ca 2p and Ca L-edge X-ray spectroscopy. A possible way to interpret the observed, obviously very favorable “special relationship” between (hydrogen)phosphates and Ca-birnessites in electrocatalytic water oxidation would be that HnPO4(3−n)− anions are incorporated into the catalyst material where they act as stabilizing units for Mn3+ highly active centers and also as “internal bases” for the protons released during the water-oxidation reaction.

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author = {Ronge, Emanuel and Lindner, Jonas and Ross, Ulrich and Melder, Jens and Ohms, Jonas and Roddatis, Vladimir and Kurz, Philipp and Jooss, Christian},
title = {Atom Surface Dynamics of Manganese Oxide under Oxygen Evolution Reaction-Like Conditions Studied by In Situ Environmental Transmission Electron Microscopy},
journal = {The Journal of Physical Chemistry C},
volume = {125},
number = {9},
pages = {5037-5047},
year = {2021},
doi = {10.1021/acs.jpcc.0c09806},
URL = {https://doi.org/10.1021/acs.jpcc.0c09806},
eprint = {https://doi.org/10.1021/acs.jpcc.0c09806}
}

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pages = {2003524},
author = {Niklas A. Weber and Hendrik Schmidt and Tim Sievert and Christian Jooss and Friedrich Güthoff and Vasily Moshneaga and Konrad Samwer and Matthias Krüger and Cynthia A. Volkert},
title = {Polaronic Contributions to Friction in a Manganite Thin Film},
journal = {Advanced Science}
}

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publisher = {American Chemical Society ({ACS})},
author = {Emanuel Ronge and Jonas Lindner and Ulrich Ross and Jens Melder and Jonas Ohms and Vladimir Roddatis and Philipp Kurz and Christian Jooss},
title = {Atom Surface Dynamics of Manganese Oxide under Oxygen Evolution Reaction-Like Conditions Studied by In Situ Environmental Transmission Electron Microscopy},
journal = {The Journal of Physical Chemistry C}
}

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title = {High-Pressure Torsion for Synthesis of High-Entropy Alloys},
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volume = {104},
author = {David Jansen and Christian Jooss and Fabian Heidrich-Meisner},
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journal = {Physical Review B},
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c
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publisher = {Elsevier {BV}},
volume = {228},
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author = {Tobias Meyer and Tobias Westphal and Birte Kressdorf and Ulrich Ross and Christian Jooss and Michael Seibt},
title = {Site-specific plan-view {Tem} lamella preparation of pristine surfaces with a large field of view},
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title = {Aberration-corrected {Stem} imaging of 2D materials: Artifacts and practical applications of threefold astigmatism},
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title = {Photoinduced Heterogeneous C-H Arylation by a Reusable Hybrid Copper Catalyst},
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title = {Structure of Nanocrystalline, Partially Disordered {MoS}2$\mathplus$$\updelta$ Derived from {Hrtem}{\textemdash}An Abundant Material for Efficient {Her} Catalysis},
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title = {Outstanding Reviewers for Energy {\&} Environmental Science in 2019},
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publisher = {American Physical Society ({APS})},
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author = {Marco Eckhoff and Florian Schönewald and Marcel Risch and Cynthia A. Volkert and Peter E. Blöchl and Jörg Behler},
title = {Closing the gap between theory and experiment for lithium manganese oxide spinels using a high-dimensional neural network potential},
journal = {Physical Review B},
pages = {174102}
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@article{10.1039/d0dt00381f,
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url = {http://dx.doi.org/10.1039/d0dt00381f},
year = 2020,
publisher = {Royal Society of Chemistry ({RSC})},
volume = {49},
pages = {8367--8374},
author = {Lucas A. Paul and Sheida Rajabi and Christian Jooss and Franc Meyer and Fatemeh Ebrahimi and Inke Siewert},
title = {A dinuclear rhenium complex in the electrochemically driven homogeneous and heterogeneous H$\mathplus$/{Co}2-reduction},
journal = {Dalton Transactions}
}

@article{10.1039/d0gc01187h,
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url = {http://dx.doi.org/10.1039/d0gc01187h},
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publisher = {Royal Society of Chemistry ({RSC})},
volume = {22},
pages = {4516--4522},
author = {Yu Zhang and Nareh Hatami and Niklas Simon Lange and Emanuel Ronge and Waldemar Schilling and Christian Jooss and Shoubhik Das},
title = {A metal-free heterogeneous photocatalyst for the selective oxidative cleavage of CC bonds in aryl olefins via harvesting direct solar energy},
journal = {Green Chemistry}
}

@article{10.1103/physrevb.102.014302,
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url = {http://dx.doi.org/10.1103/physrevb.102.014302},
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publisher = {American Physical Society ({APS})},
volume = {102},
author = {Sangeeta Rajpurohit and Christian Jooss and Peter E. Blöchl},
title = {Evolution of the magnetic and polaronic order of 
Pr1/2Ca1/2MnO3
following an ultrashort light pulse},
journal = {Physical Review B},
pages = {014302}
}

@article{10.1038/s43246-020-00070-6,
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title = {Dynamic observation of manganese adatom mobility at perovskite oxide catalyst interfaces with water},
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@article{10.1103/physrevapplied.14.054006,
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publisher = {American Physical Society ({APS})},
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title = {Room-Temperature Hot-Polaron Photovoltaics in the Charge-Ordered State of a Layered Perovskite Oxide Heterojunction},
journal = {Physical Review Applied},
pages = {054006}
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url = {http://dx.doi.org/10.1021/acscatal.0c01577},
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publisher = {American Chemical Society ({ACS})},
volume = {10},
pages = {10614--10626},
author = {Sheida Rajabi and Fatemeh Ebrahimi and Gaurav Lole and Jann Odrobina and Sebastian Dechert and Christian Jooss and Franc Meyer},
title = {Water Oxidizing Diruthenium Electrocatalysts Immobilized on Carbon Nanotubes: Effects of the Number and Positioning of Pyrene Anchors},
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@article{Rajpurohit_2020,
	doi = {10.1103/physrevb.102.174430},  
	url = {https://doi.org/10.1103%2Fphysrevb.102.174430},  
	year = 2020,
	month = {nov},  
	publisher = {American Physical Society ({APS})},  
	volume = {102},  
	number = {17},  
	author = {Sangeeta Rajpurohit and Liang Z. Tan and Christian Jooss and P. E. Blöchl},  
	title = {Ultrafast spin-nematic and ferroelectric phase transitions induced by femtosecond light pulses},  
	journal = {Physical Review B}
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@article{PhysRevApplied.14.054006,
  title = {Room-Temperature Hot-Polaron Photovoltaics in the Charge-Ordered State of a Layered Perovskite Oxide Heterojunction},
  author = {Kressdorf, B. and Meyer, T. and Belenchuk, A. and Shapoval, O. and ten Brink, M. and Melles, S. and Ross, U. and Hoffmann, J. and Moshnyaga, V. and Seibt, M. and Bl\"ochl, P. and Jooss, C.},
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  year = {2020},
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  publisher = {American Physical Society},
  doi = {10.1103/PhysRevApplied.14.054006},
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}

@article{doi:10.1021/acscatal.0c01577,
author = {Rajabi, Sheida and Ebrahimi, Fatemeh and Lole, Gaurav and Odrobina, Jann and Dechert, Sebastian and Jooss, Christian and Meyer, Franc},
title = {Water Oxidizing Diruthenium Electrocatalysts Immobilized on Carbon Nanotubes: Effects of the Number and Positioning of Pyrene Anchors},
journal = {ACS Catalysis},
volume = {10},
number = {18},
pages = {10614-10626},
year = {2020},
doi = {10.1021/acscatal.0c01577},
URL = {https://doi.org/10.1021/acscatal.0c01577},
eprint = {https://doi.org/10.1021/acscatal.0c01577}
}

@article{PhysRevB.102.014302,
  title = {Evolution of the magnetic and polaronic order of ${\mathrm{Pr}}_{1/2}{\mathrm{Ca}}_{1/2}{\mathrm{MnO}}_{3}$ following an ultrashort light pulse},
  author = {Rajpurohit, Sangeeta and Jooss, Christian and Bl\"ochl, Peter E.},
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  volume = {102},
  issue = {1},
  pages = {014302},
  numpages = {23},
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  doi = {10.1103/PhysRevB.102.014302},
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}

@article{ubt_eref86179,
           title = {A metal-free heterogeneous photocatalyst for the selective oxidative cleavage of C=C bonds in aryl olefins via harvesting direct solar energy},
           pages = {4516--4522},
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            year = {2020},
          number = {14},
         journal = {Green Chemistry},
            issn = {1463-9262},
          author = {Zhang, Yu and Hatami, Nareh and Lange, Niklas Simon and Ronge, Emanuel and Schilling, Waldemar and Jooss, Christian and Das, Shoubhik},
             url = {https://eref.uni-bayreuth.de/id/eprint/86179/}
}

@Article{D0DT00381F,
author ="Paul, Lucas A. and Rajabi, Sheida and Jooss, Christian and Meyer, Franc and Ebrahimi, Fatemeh and Siewert, Inke",
title  ="A dinuclear rhenium complex in the electrochemically driven homogeneous and heterogeneous H+/CO2-reduction",
journal  ="Dalton Trans.",
year  ="2020",
volume  ="49",
issue  ="24",
pages  ="8367-8374",
publisher  ="The Royal Society of Chemistry",
doi  ="10.1039/D0DT00381F",
url  ="http://dx.doi.org/10.1039/D0DT00381F",
abstract  ="A dinculear Re(CO)3 complex with a proton responsive phenol unit and a pyrene anchor in the ligand backbone was investigated in the electrochemical CO2/H+ conversion in solution and adsorbed on multi walled carbon nanotubes (MWCNT) on an GC electrode surface. The pyrene group unit is introduced at the end of the ligand synthesis via a coupling reaction{,} which allows for a versatile ligand modification in order to tune the electronic properties or to introduce various anchor groups for heterogenisation at a late stage. The redox chemistry of the pyrene-α-diimine-Re(CO)3 complex{,} 1{,} was investigated in N{,}N-dimethylformamide (dmf){,} including IR-spectroelectrochemical (IR-SEC) characterisation of the short lived{,} reduced species. Subsequently{,} the electrochemical H+/CO2-reduction catalysis in dmf/water was investigated. The complex catalyses syngas formation yielding CO and H2 with similar rates{,} namely in Faraday yields of 45% and 35%{,} respectively. Since the similar complex without the pyrene anchor in the backbone{,} I{,} prefers CO2 over H+ reduction{,} the formation of syngas was rationalised by the small differences in the redox properties and pKa values of the phenol-pyrene unit in regard to phenol unit as in I. Subsequently{,} the complex was adsorbed on multi walled carbon nanotubes (MWCNT) on a GC electrode surface. Scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS) confirmed coating of the electrode. The immobilised complex was utilised in the electrochemical CO2/H+ reduction in dmf/water{,} however{,} the complex quickly desorbed under reductive conditions{,} likely due to the good solubility of the reduced species. Water as a solvent prevents desorption as confirmed by XPS{,} however{,} then a preference for H2 formation over syngas formation was observed under electrocatalytic conditions. Thus{,} these experiments show{,} that the results obtained in aqueous organic solution are not easily transferable to the heterogeneous systems operating in water due to changes in the reaction rates for competing pathways."
}

A dinculear Re(CO)3 complex with a proton responsive phenol unit and a pyrene anchor in the ligand backbone was investigated in the electrochemical CO2/H+ conversion in solution and adsorbed on multi walled carbon nanotubes (MWCNT) on an GC electrode surface. The pyrene group unit is introduced at the end of the ligand synthesis via a coupling reaction, which allows for a versatile ligand modification in order to tune the electronic properties or to introduce various anchor groups for heterogenisation at a late stage. The redox chemistry of the pyrene-α-diimine-Re(CO)3 complex, 1, was investigated in N,N-dimethylformamide (dmf), including IR-spectroelectrochemical (IR-SEC) characterisation of the short lived, reduced species. Subsequently, the electrochemical H+/CO2-reduction catalysis in dmf/water was investigated. The complex catalyses syngas formation yielding CO and H2 with similar rates, namely in Faraday yields of 45% and 35%, respectively. Since the similar complex without the pyrene anchor in the backbone, I, prefers CO2 over H+ reduction, the formation of syngas was rationalised by the small differences in the redox properties and pKa values of the phenol-pyrene unit in regard to phenol unit as in I. Subsequently, the complex was adsorbed on multi walled carbon nanotubes (MWCNT) on a GC electrode surface. Scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS) confirmed coating of the electrode. The immobilised complex was utilised in the electrochemical CO2/H+ reduction in dmf/water, however, the complex quickly desorbed under reductive conditions, likely due to the good solubility of the reduced species. Water as a solvent prevents desorption as confirmed by XPS, however, then a preference for H2 formation over syngas formation was observed under electrocatalytic conditions. Thus, these experiments show, that the results obtained in aqueous organic solution are not easily transferable to the heterogeneous systems operating in water due to changes in the reaction rates for competing pathways.

@article{doi:10.1021/acs.jpcc.0c00840,
author = {Busse, Philipp and Yin, Zhong and Mierwaldt, Daniel and Scholz, Julius and Kressdorf, Birte and Glaser, Leif and Miedema, Piter S. and Rothkirch, André and Viefhaus, Jens and Jooss, Christian and Techert, Simone and Risch, Marcel},
title = {Probing the Surface of La0.6Sr0.4MnO3 in Water Vapor by In Situ Photon-In/Photon-Out Spectroscopy},
journal = {The Journal of Physical Chemistry C},
volume = {124},
number = {14},
pages = {7893-7902},
year = {2020},
doi = {10.1021/acs.jpcc.0c00840},
URL = {https://doi.org/10.1021/acs.jpcc.0c00840},
eprint = {https://doi.org/10.1021/acs.jpcc.0c00840}
}

@Article{catal10080856,
AUTHOR = {Ronge, Emanuel and Hildebrandt, Sonja and Grutza, Marie-Luise and Klein, Helmut and Kurz, Philipp and Jooss, Christian},
TITLE = {Structure of Nanocrystalline, Partially Disordered MoS2+δ Derived from HRTEM—An Abundant Material for Efficient HER Catalysis},
JOURNAL = {Catalysts},
VOLUME = {10},
YEAR = {2020},
NUMBER = {8},
ARTICLE-NUMBER = {856},
URL = {https://www.mdpi.com/2073-4344/10/8/856},
ISSN = {2073-4344},
ABSTRACT = {Molybdenum sulfides (MoSx, x > 2) are promising catalysts for the hydrogen evolution reaction (HER) that show high hydrogen evolution rates and potentially represent an abundant alternative to platinum. However, a complete understanding of the structure of the most active variants is still lacking. Nanocrystalline MoS2+δ was prepared by a solvothermal method and immobilized on graphene. The obtained electrodes exhibit stable HER current densities of 3 mA cm−2 at an overpotential of ~200 mV for at least 7 h. A structural analysis of the material by high-resolution transmission electron microscopy (HRTEM) show partially disordered nanocrystals of a size between 5–10 nm. Both X-ray and electron diffraction reveal large fluctuations in lattice spacing, where the average c-axis stacking is increased and the in-plane lattice parameter is locally reduced in comparison to the layered structure of crystalline MoS2. A three-dimensional structural model of MoS2+δ could be derived from the experiments, in which [Mo2S12]2− and [Mo3S13]2− clusters as well as disclinations represent the typical defects in the ideal MoS2 structure. It is suggested that the partially disordered nanostructure leads to a high density of coordinatively modified Mo sites with lower Mo–Mo distances representing the active sites for HER catalysis, and, that these structural features are more important than the S:Mo ratio for the activity.},
DOI = {10.3390/catal10080856}
}

Molybdenum sulfides (MoSx, x > 2) are promising catalysts for the hydrogen evolution reaction (HER) that show high hydrogen evolution rates and potentially represent an abundant alternative to platinum. However, a complete understanding of the structure of the most active variants is still lacking. Nanocrystalline MoS2+δ was prepared by a solvothermal method and immobilized on graphene. The obtained electrodes exhibit stable HER current densities of 3 mA cm−2 at an overpotential of  200 mV for at least 7 h. A structural analysis of the material by high-resolution transmission electron microscopy (HRTEM) show partially disordered nanocrystals of a size between 5–10 nm. Both X-ray and electron diffraction reveal large fluctuations in lattice spacing, where the average c-axis stacking is increased and the in-plane lattice parameter is locally reduced in comparison to the layered structure of crystalline MoS2. A three-dimensional structural model of MoS2+δ could be derived from the experiments, in which [Mo2S12]2− and [Mo3S13]2− clusters as well as disclinations represent the typical defects in the ideal MoS2 structure. It is suggested that the partially disordered nanostructure leads to a high density of coordinatively modified Mo sites with lower Mo–Mo distances representing the active sites for HER catalysis, and, that these structural features are more important than the S:Mo ratio for the activity.

@article{CottreWelterRongeSmirnovFingerJoossKaiserJaegermann+2020+1155+1169,
url = {https://doi.org/10.1515/zpch-2019-1483},
title = {Integrated Devices for Photoelectrochemical Water Splitting Using Adapted Silicon Based Multi-Junction Solar Cells Protected by ALD TiO2 Coatings},
title = {},
author = {Thorsten Cottre and Katharina Welter and Emanuel Ronge and Vladimir Smirnov and Friedhelm Finger and Christian Jooss and Bernhard Kaiser and Wolfram Jaegermann},
pages = {1155--1169},
volume = {234},
number = {6},
journal = {Zeitschrift für Physikalische Chemie},
doi = {doi:10.1515/zpch-2019-1483},
year = {2020},
lastchecked = {2023-08-30}
}

@article{https://doi.org/10.1002/chem.202000192,
author = {Choi, Isaac and Müller, Valentin and Lole, Gaurav and Köhler, Robert and Karius, Volker and Viöl, Wolfgang and Jooss, Christian and Ackermann, Lutz},
title = {Photoinduced Heterogeneous C−H Arylation by a Reusable Hybrid Copper Catalyst},
journal = {Chemistry – A European Journal},
volume = {26},
number = {16},
pages = {3509-3514},
keywords = {C−H arylation, copper catalysis, heterogeneous catalysis, hybrid catalysis, photocatalysis},
doi = {https://doi.org/10.1002/chem.202000192},
url = {https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/chem.202000192},
eprint = {https://chemistry-europe.onlinelibrary.wiley.com/doi/pdf/10.1002/chem.202000192},
abstract = {Abstract Heterogeneous copper catalysis enabled photoinduced C−H arylations under exceedingly mild conditions at room temperature. The versatile hybrid copper catalyst provided step-economical access to arylated heteroarenes, terpenes and alkaloid natural products with various aryl halides. The hybrid copper catalyst could be reused without significant loss of catalytic efficacy. Detailed studies in terms of TEM, HRTEM and XPS analysis of the hybrid copper catalyst, among others, supported its outstanding stability and reusability.},
year = {2020}
}

Abstract Heterogeneous copper catalysis enabled photoinduced C−H arylations under exceedingly mild conditions at room temperature. The versatile hybrid copper catalyst provided step-economical access to arylated heteroarenes, terpenes and alkaloid natural products with various aryl halides. The hybrid copper catalyst could be reused without significant loss of catalytic efficacy. Detailed studies in terms of TEM, HRTEM and XPS analysis of the hybrid copper catalyst, among others, supported its outstanding stability and reusability.

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}

@article{10.1021/acs.jpcc.0c00840,
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year = 2020,
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author = {Philipp Busse and Zhong Yin and Daniel Mierwaldt and Julius Scholz and Birte Kressdorf and Leif Glaser and Piter S. Miedema and Andre Rothkirch and Jens Viefhaus and Christian Jooss and Simone Agnes Techert and Marcel Risch},
title = {Probing the Surface of La0.6Sr0.4MnO3 in Water Vapor by In Situ Photon-In / Photon-Out Spectroscopy},
journal = {The Journal of Physical Chemistry C}
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@article{10.1515/zpch-2019-1483,
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url = {http://dx.doi.org/10.1515/zpch-2019-1483},
year = 2020,
publisher = {Walter de Gruyter {GmbH}},
volume = {0},
author = {Thorsten Cottre and Katharina Welter and Emanuel Ronge and Vladimir Smirnov and Friedhelm Finger and Christian Jooss and Bernhard Kaiser and Wolfram Jaegermann},
title = {Integrated Devices for Photoelectrochemical Water Splitting Using Adapted Silicon Based Multi-Junction Solar Cells Protected by {Ald} {TiO}2 Coatings},
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author = {F. Rieger and V. Roddatis and K. Kaiser and G. Bendt and S. Schulz and C. Jooss},
title = {Transition into a phonon glass in crystalline thermoelectric 
(Sb1-{xBix})2Te3
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}

@article{Doring:ve5095,
author = "D{\"{o}}ring, Florian and Risch, Marcel and R{\"{o}}sner, Benedikt and Beye, Martin and Busse, Philipp and Kubi{\v{c}}ek, Katharina and Glaser, Leif and Miedema, Piter S. and Soltau, Jakob and Raiser, Dirk and Guzenko, Vitaliy A. and Szabadics, Lukas and Kochanneck, Leif and Baumung, Max and Buck, Jens and Jooss, Christian and Techert, Simone and David, Christian",
title = "{A zone-plate-based two-color spectrometer for indirect X-ray absorption spectroscopy}",
journal = "Journal of Synchrotron Radiation",
year = "2019",
volume = "26",
number = "4",
pages = "1266--1271",
month = "Jul",
doi = {10.1107/S1600577519003898},
url = {https://doi.org/10.1107/S1600577519003898},
abstract = {X-ray absorption spectroscopy (XAS) is a powerful element-specific technique that allows the study of structural and chemical properties of matter. Often an indirect method is used to access the X-ray absorption (XA). This work demonstrates a new XAS implementation that is based on off-axis transmission Fresnel zone plates to obtain the XA spectrum of La${\sb 0.6}$Sr${\sb 0.4}$MnO${\sb 3}$ by analysis of three emission lines simultaneously at the detector, namely the O 2{\it p}{--}1{\it s}, Mn 3{\it s}{--}2{\it p} and Mn 3{\it d}{--}2{\it p} transitions. This scheme allows the simultaneous measurement of an integrated total fluorescence yield and the partial fluorescence yields (PFY) of the Mn 3{\it s}{--}2{\it p} and Mn 3{\it d}{--}2{\it p} transitions when scanning the Mn {\it L}-edge. In addition to this, the reduction in O fluorescence provides another measure for absorption often referred to as the inverse partial fluorescence yield (IPFY). Among these different methods to measure XA, the Mn 3{\it s} PFY and IPFY deviate the least from the true XA spectra due to the negligible influence of selection rules on the decay channel. Other advantages of this new scheme are the potential to strongly increase the efficiency and throughput compared with similar measurements using conventional gratings and to increase the signal-to-noise of the XA spectra as compared with a photodiode. The ability to record undistorted bulk XA spectra at high flux is crucial for future {\it in situ} spectroscopy experiments on complex materials.},
keywords = {two-color X-ray absorption spectroscopy, zone plates, soft X-rays},
}

X-ray absorption spectroscopy (XAS) is a powerful element-specific technique that allows the study of structural and chemical properties of matter. Often an indirect method is used to access the X-ray absorption (XA). This work demonstrates a new XAS implementation that is based on off-axis transmission Fresnel zone plates to obtain the XA spectrum of La${\sb 0.6}$Sr${\sb 0.4}$MnO${\sb 3}$ by analysis of three emission lines simultaneously at the detector, namely the O 2ıt p–1ıt s, Mn 3ıt s–2ıt p and Mn 3ıt d–2ıt p transitions. This scheme allows the simultaneous measurement of an integrated total fluorescence yield and the partial fluorescence yields (PFY) of the Mn 3ıt s–2ıt p and Mn 3ıt d–2ıt p transitions when scanning the Mn ıt L-edge. In addition to this, the reduction in O fluorescence provides another measure for absorption often referred to as the inverse partial fluorescence yield (IPFY). Among these different methods to measure XA, the Mn 3ıt s PFY and IPFY deviate the least from the true XA spectra due to the negligible influence of selection rules on the decay channel. Other advantages of this new scheme are the potential to strongly increase the efficiency and throughput compared with similar measurements using conventional gratings and to increase the signal-to-noise of the XA spectra as compared with a photodiode. The ability to record undistorted bulk XA spectra at high flux is crucial for future ıt in situ spectroscopy experiments on complex materials.

@Article{catal9090751,
AUTHOR = {Roddatis, Vladimir and Lole, Gaurav and Jooss, Christian},
TITLE = {In Situ Preparation of Pr1-xCaxMnO3 and La1-xSrxMnO3 Catalysts Surface for High-Resolution Environmental Transmission Electron Microscopy},
JOURNAL = {Catalysts},
VOLUME = {9},
YEAR = {2019},
NUMBER = {9},
ARTICLE-NUMBER = {751},
URL = {https://www.mdpi.com/2073-4344/9/9/751},
ISSN = {2073-4344},
ABSTRACT = {The study of changes in the atomic structure of a catalyst under chemical reaction conditions is extremely important for understanding the mechanism of their operation. For in situ environmental transmission electron microscopy (ETEM) studies, this requires preparation of electron transparent ultrathin TEM lamella without surface damage. Here, thin films of Pr1-xCaxMnO3 (PCMO, x = 0.1, 0.33) and La1-xSrxMnO3 (LSMO, x = 0.4) perovskites are used to demonstrate a cross-section specimen preparation method, comprised of two steps. The first step is based on optimized focused ion beam cutting procedures using a photoresist protection layer, finally being removed by plasma-etching. The second step is applicable for materials susceptible to surface amorphization, where in situ recrystallization back to perovskite structure is achieved by using electron beam driven chemistry in gases. This requires reduction of residual water vapor in a TEM column. Depending on the gas environment, long crystalline facets having different atomic terminations and Mn-valence state, can be prepared.},
DOI = {10.3390/catal9090751}
}

The study of changes in the atomic structure of a catalyst under chemical reaction conditions is extremely important for understanding the mechanism of their operation. For in situ environmental transmission electron microscopy (ETEM) studies, this requires preparation of electron transparent ultrathin TEM lamella without surface damage. Here, thin films of Pr1-xCaxMnO3 (PCMO, x = 0.1, 0.33) and La1-xSrxMnO3 (LSMO, x = 0.4) perovskites are used to demonstrate a cross-section specimen preparation method, comprised of two steps. The first step is based on optimized focused ion beam cutting procedures using a photoresist protection layer, finally being removed by plasma-etching. The second step is applicable for materials susceptible to surface amorphization, where in situ recrystallization back to perovskite structure is achieved by using electron beam driven chemistry in gases. This requires reduction of residual water vapor in a TEM column. Depending on the gas environment, long crystalline facets having different atomic terminations and Mn-valence state, can be prepared.

@article{Meyer_2019,
doi = {10.1088/1742-6596/1190/1/012009},
url = {https://dx.doi.org/10.1088/1742-6596/1190/1/012009},
year = {2019},
month = {may},
publisher = {IOP Publishing},
volume = {1190},
number = {1},
pages = {012009},
author = {T Meyer and B Kressdorf and J Lindner and P Peretzki and V Roddatis and C Jooss and M Seibt},
title = {High-resolution Scanning Transmission EBIC Analysis of Misfit Dislocations at Perovskite pn-Heterojunctions},
journal = {Journal of Physics: Conference Series},
abstract = {Fundamental losses of photovoltaic energy conversion are transmission of sub band gap photons and thermalisation which are the underlying physics of the Shockley-Queisser limit defining maximum conversion efficiency of single-junction solar cells. Strongly correlated materials such as perovskites are promising candidates to exceed this limit by exploiting (i) long wavelength light absorption and (ii) the existence of long-living intraband excitations indicating that harvesting hot excess carriers might be feasible in such systems. In this work, we study pn-heterojunctions produced from Pr1-xCaxMnO3 on SrTi1-yNbyO3 by means of microscopic techniques. Such systems exhibit relevant quantities such as space charge layer width, screening lengths and excess carrier diffusion lengths in the 1-10 nm range which makes the use of standard methods such as electron beam induced current a challenging task. We report scanning transmission electron beam induced current experiments of misfit dislocations at the heterojunction. The dislocation-induced reduction of the charge collection is studied with nanometer spatial resolution. Effects of surface recombination and the heterojunction electric field are discussed.}
}

Fundamental losses of photovoltaic energy conversion are transmission of sub band gap photons and thermalisation which are the underlying physics of the Shockley-Queisser limit defining maximum conversion efficiency of single-junction solar cells. Strongly correlated materials such as perovskites are promising candidates to exceed this limit by exploiting (i) long wavelength light absorption and (ii) the existence of long-living intraband excitations indicating that harvesting hot excess carriers might be feasible in such systems. In this work, we study pn-heterojunctions produced from Pr1-xCaxMnO3 on SrTi1-yNbyO3 by means of microscopic techniques. Such systems exhibit relevant quantities such as space charge layer width, screening lengths and excess carrier diffusion lengths in the 1-10 nm range which makes the use of standard methods such as electron beam induced current a challenging task. We report scanning transmission electron beam induced current experiments of misfit dislocations at the heterojunction. The dislocation-induced reduction of the charge collection is studied with nanometer spatial resolution. Effects of surface recombination and the heterojunction electric field are discussed.

@article{https://doi.org/10.1002/batt.201800119,
author = {Köhler, Lennart and Szabadics, Lukas and Jooss, Christian and Risch, Marcel},
title = {Peroxide Yield of the (001) La0.6Sr0.4MnO3 Surface as a Bifunctional Electrocatalyst for the Oxygen Reduction Reaction and Oxygen Evolution Reaction in Alkaline Media},
journal = {Batteries \& Supercaps},
volume = {2},
number = {4},
pages = {364-372},
keywords = {bifunctional catalysts, model electrode, oxygen reduction, peroxide, RRDE},
doi = {https://doi.org/10.1002/batt.201800119},
url = {https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/batt.201800119},
eprint = {https://chemistry-europe.onlinelibrary.wiley.com/doi/pdf/10.1002/batt.201800119},
abstract = {Abstract Active and stable bifunctional electrocatalysts are required for large-scale deployment of rechargeable metal-air and metal-O2 batteries. This is hindered by the large overpotentials of the oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) in alkaline media, where peroxide is an undesired side product. We study the suitability of epitaxial (001)-oriented La0.6Sr0.4MnO3 perovskite surfaces as a bifunctional catalyst using a rotating-ring disk electrode (RRDE) assembly and focus particularly on the selectivity of the ORR. The peroxide yield is above 50 \% during ORR-only investigations in the scan range of 0.69 to 0.99 V vs. RHE where the CV traces are reproducible. In contrast, the peroxide yield is drastically reduced during OER-ORR cycling where a peroxide yield below 10 \% is reached during the ORR in the scan range of 0.74 V to 1.74 V vs. RHE. Our study highlights the importance of the electrode history and thus clearly demonstrates that separate studies of the OER and ORR are insufficient to optimize bifunctional electrocatalysts.},
year = {2019}
}

Abstract Active and stable bifunctional electrocatalysts are required for large-scale deployment of rechargeable metal-air and metal-O2 batteries. This is hindered by the large overpotentials of the oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) in alkaline media, where peroxide is an undesired side product. We study the suitability of epitaxial (001)-oriented La0.6Sr0.4MnO3 perovskite surfaces as a bifunctional catalyst using a rotating-ring disk electrode (RRDE) assembly and focus particularly on the selectivity of the ORR. The peroxide yield is above 50 % during ORR-only investigations in the scan range of 0.69 to 0.99 V vs. RHE where the CV traces are reproducible. In contrast, the peroxide yield is drastically reduced during OER-ORR cycling where a peroxide yield below 10 % is reached during the ORR in the scan range of 0.74 V to 1.74 V vs. RHE. Our study highlights the importance of the electrode history and thus clearly demonstrates that separate studies of the OER and ORR are insufficient to optimize bifunctional electrocatalysts.

@article{10.1002/adfm.201808270,
doi = {10.1002/adfm.201808270},
url = {http://dx.doi.org/10.1002/adfm.201808270},
year = 2019,
publisher = {Wiley},
pages = {1808270},
author = {Marius Keunecke and Fryderyk Lyzwa and Danny Schwarzbach and Vladimir Roddatis and Nicolas Gauquelin and Knut Müller-Caspary and Johann Verbeeck and Sara J. Callori and Frank Klose and Markus Jungbauer and Vasily Moshnyaga},
title = {High-T
C
Interfacial Ferromagnetism in {SrMnO}3
/{LaMnO}3
Superlattices},
journal = {Advanced Functional Materials}
}

@article{10.1039/c8se00551f,
doi = {10.1039/c8se00551f},
url = {http://dx.doi.org/10.1039/c8se00551f},
year = 2019,
publisher = {Royal Society of Chemistry ({RSC})},
author = {Max Baumung and Florian Schönewald and Torben Erichsen and Cynthia A. Volkert and Marcel Risch},
title = {Influence of particle size on the apparent electrocatalytic activity of {LiMn}2O4 for oxygen evolution},
journal = {Sustainable Energy {\&} Fuels}
}

@article{10.1088/1742-6596/1190/1/012009,
doi = {10.1088/1742-6596/1190/1/012009},
url = {http://dx.doi.org/10.1088/1742-6596/1190/1/012009},
year = 2019,
publisher = {{IOP} Publishing},
volume = {1190},
pages = {012009},
author = {T Meyer and B Kressdorf and J Lindner and P Peretzki and V Roddatis and C Jooss and M Seibt},
title = {High-resolution Scanning Transmission {Ebic} Analysis of Misfit Dislocations at Perovskite pn-Heterojunctions},
journal = {Journal of Physics: Conference Series}
}

@article{10.1002/adma.201806296,
doi = {10.1002/adma.201806296},
url = {http://dx.doi.org/10.1002/adma.201806296},
year = 2019,
publisher = {Wiley},
pages = {1806296},
author = {Chao Wei and Reshma R. Rao and Jiayu Peng and Botao Huang and Ifan E. L. Stephens and Marcel Risch and Zhichuan J. Xu and Yang Shao-Horn},
title = {Recommended Practices and Benchmark Activity for Hydrogen and Oxygen Electrocatalysis in Water Splitting and Fuel Cells},
journal = {Advanced Materials}
}

@article{10.3390/catal9090751,
doi = {10.3390/catal9090751},
url = {http://dx.doi.org/10.3390/catal9090751},
year = 2019,
publisher = {{MDPI} {AG}},
volume = {9},
pages = {751},
author = {Roddatis and  Lole and  Jooss},
title = {In Situ Preparation of Pr1-{xCaxMnO}3 and La1-{xSrxMnO}3 Catalysts Surface for High-Resolution Environmental Transmission Electron Microscopy},
journal = {Catalysts}
}

@article{10.1016/j.ultramic.2017.08.012,
doi = {10.1016/j.ultramic.2017.08.012},
url = {http://dx.doi.org/10.1016/j.ultramic.2017.08.012},
year = 2018,
publisher = {Elsevier {BV}},
volume = {184},
pages = {61--70},
author = {Thilo Kramer and Daniel Mierwaldt and Malte Scherff and Mike Kanbach and Christian Jooss},
title = {Developing an in situ environmental {Tem} set up for investigations of resistive switching mechanisms in Pt-Pr1-{xCaxMnO}3-$\updelta$-Pt sandwich structures},
journal = {Ultramicroscopy}
}

@article{10.1088/1361-6641/aad7a3,
doi = {10.1088/1361-6641/aad7a3},
url = {http://dx.doi.org/10.1088/1361-6641/aad7a3},
year = 2018,
publisher = {{IOP} Publishing},
volume = {33},
pages = {105002},
author = {Georg Bendt and Kevin Kaiser and Alla Heckel and Felix Rieger and Dennis Oing and Axel Lorke and Nicolas Perez Rodriguez and Gabi Schierning and Christian Jooss and Stephan Schulz},
title = {Structural and thermoelectrical characterization of epitaxial Sb2Te3 high quality thin films grown by thermal evaporation},
journal = {Semiconductor Science and Technology}
}

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doi = {10.3390/met8121085},
url = {http://dx.doi.org/10.3390/met8121085},
year = 2018,
publisher = {{MDPI} {AG}},
volume = {8},
pages = {1085},
author = {Lin Tian and Cynthia A. Volkert},
title = {Measuring Structural Heterogeneities in Metallic Glasses Using Transmission Electron Microscopy},
journal = {Metals}
}

@article{10.1016/j.tca.2018.08.006,
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url = {http://dx.doi.org/10.1016/j.tca.2018.08.006},
year = 2018,
publisher = {Elsevier {BV}},
volume = {668},
pages = {116--125},
author = {Emanuel Franke and David A. LaVan and Cynthia A. Volkert},
title = {Quantifying {Dc} differential scanning nanocalorimetry for determining heat capacities},
journal = {Thermochimica Acta}
}

@article{10.1016/j.scriptamat.2017.11.033,
doi = {10.1016/j.scriptamat.2017.11.033},
url = {http://dx.doi.org/10.1016/j.scriptamat.2017.11.033},
year = 2018,
publisher = {Elsevier {BV}},
volume = {146},
pages = {150--153},
author = {K.R. Mangipudi and E. Epler and C.A. Volkert},
title = {On the multiaxial yielding and hardness to yield stress relation of nanoporous gold},
journal = {Scripta Materialia}
}

@article{10.1016/j.ijhydene.2017.11.101,
doi = {10.1016/j.ijhydene.2017.11.101},
url = {http://dx.doi.org/10.1016/j.ijhydene.2017.11.101},
year = 2018,
publisher = {Elsevier {BV}},
volume = {43},
pages = {1634--1642},
author = {Niklas Teichmann and Magnus Hamm and Astrid Pundt},
title = {Fast lateral hydrogen diffusion in magnesium-hydride films on sapphire substrates studied by electrochemical hydrogenography},
journal = {International Journal of Hydrogen Energy}
}

@article{10.1021/acs.jpcc.8b02692,
doi = {10.1021/acs.jpcc.8b02692},
url = {http://dx.doi.org/10.1021/acs.jpcc.8b02692},
year = 2018,
publisher = {American Chemical Society ({ACS})},
volume = {122},
pages = {10096--10102},
author = {Yvonne Dorenkamp and Christian Volkmann and Vladimir Roddatis and Sven Schneider and Alec M. Wodtke and Oliver Bünermann},
title = {Inelastic H Atom Scattering from Ultrathin Aluminum Oxide Films Grown by Atomic Layer Deposition on Pt(111)},
journal = {The Journal of Physical Chemistry C}
}

@article{10.1088/1361-6463/aaac64,
doi = {10.1088/1361-6463/aaac64},
url = {http://dx.doi.org/10.1088/1361-6463/aaac64},
year = 2018,
publisher = {{IOP} Publishing},
volume = {51},
pages = {125306},
author = {F Lyzwa and P Marsik and V Roddatis and C Bernhard and M Jungbauer and V Moshnyaga},
title = {In situ monitoring of atomic layer epitaxy via optical ellipsometry},
journal = {Journal of Physics D: Applied Physics}
}

@article{10.1021/acsomega.8b00833,
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url = {http://dx.doi.org/10.1021/acsomega.8b00833},
year = 2018,
publisher = {American Chemical Society ({ACS})},
volume = {3},
pages = {6841--6848},
author = {Bo Pang and Robert Köhler and Vladimir Roddatis and Huan Liu and Xiaohui Wang and Wolfgang Viöl and Kai Zhang},
title = {One-Step Synthesis of Quadrilateral-Shaped Silver Nanoplates with Lamellar Structures Tuned by Amylopectin Derivatives},
journal = {{ACS} Omega}
}

@article{10.1016/j.jcrysgro.2018.03.021,
doi = {10.1016/j.jcrysgro.2018.03.021},
url = {http://dx.doi.org/10.1016/j.jcrysgro.2018.03.021},
year = 2018,
publisher = {Elsevier {BV}},
volume = {490},
pages = {77--83},
author = {Georg Bendt and Sanae Gassa and Felix Rieger and Christian Jooss and Stephan Schulz},
title = {Low-temperature {Mocvd} deposition of Bi 2 Te 3  thin films using Et 2 {BiTeEt} as single source precursor},
journal = {Journal of Crystal Growth}
}

@article{10.1021/acs.jpclett.8b02363,
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year = 2018,
publisher = {American Chemical Society ({ACS})},
volume = {9},
pages = {5246--5253},
author = {Vladimir Roddatis and Marian D. Bongers and Richard Vink and Vladimir Burlaka and Jakub {\v{C}}{\'{\i}}{\v{z}}ek and Astrid Pundt},
title = {Insights into Hydrogen Gas Environment-Promoted Nanostructural Changes in Stressed and Relaxed Palladium by Environmental Transmission Electron Microscopy and Variable-Energy Positron Annihilation Spectroscopy},
journal = {The Journal of Physical Chemistry Letters}
}

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year = 2018,
publisher = {Elsevier {BV}},
volume = {21},
pages = {527--536},
author = {Olivier Guillon and Christian Elsässer and Oliver Gutfleisch and Jürgen Janek and Sandra Korte-Kerzel and Dierk Raabe and Cynthia A. Volkert},
title = {Manipulation of matter by electric and magnetic fields: Toward novel synthesis and processing routes of inorganic materials},
journal = {Materials Today}
}

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doi = {10.1002/cssc.201801678},
url = {http://dx.doi.org/10.1002/cssc.201801678},
year = 2018,
publisher = {Wiley},
volume = {11},
pages = {3581--3585},
author = {Peiwen Liu and Bo Pang and Lin Tian and Timmy Schäfer and Torsten Gutmann and Huan Liu and Cynthia A. Volkert and Gerd Buntkowsky and Kai Zhang},
title = {Efficient, Self-Terminating Isolation of Cellulose Nanocrystals through Periodate Oxidation in Pickering Emulsions},
journal = {{ChemSusChem}}
}

@article{10.1103/physrevb.98.134433,
doi = {10.1103/physrevb.98.134433},
url = {http://dx.doi.org/10.1103/physrevb.98.134433},
year = 2018,
publisher = {American Physical Society ({APS})},
volume = {98},
author = {Ch. Meyer and V. Roddatis and P. Ksoll and B. Damaschke and V. Moshnyaga},
title = {Structure, magnetism, and spin-phonon coupling in heteroepitaxial 
La2CoMnO6/Al2O3(0001)
films},
journal = {Physical Review B},
pages = {134433}
}

@article{10.1021/acsami.8b01903,
doi = {10.1021/acsami.8b01903},
url = {http://dx.doi.org/10.1021/acsami.8b01903},
year = 2018,
publisher = {American Chemical Society ({ACS})},
volume = {10},
pages = {14160--14169},
author = {Daniele Pergolesi and Elisa Gilardi and Emiliana Fabbri and Vladimir Roddatis and George F. Harrington and Thomas Lippert and John A. Kilner and Enrico Traversa},
title = {Interface Effects on the Ionic Conductivity of Doped Ceria-Yttria-Stabilized Zirconia Heterostructures},
journal = {{ACS} Applied Materials {\&} Interfaces}
}

@article{10.1103/physrevb.97.205121,
doi = {10.1103/physrevb.97.205121},
url = {http://dx.doi.org/10.1103/physrevb.97.205121},
year = 2018,
publisher = {American Physical Society ({APS})},
volume = {97},
author = {S. Esser and C. F. Chang and C.-Y. Kuo and S. Merten and V. Roddatis and T. D. Ha and A. Jesche and V. Moshnyaga and H.-J. Lin and A. Tanaka and C. T. Chen and L. H. Tjeng and P. Gegenwart},
title = {Strain-induced changes of the electronic properties of B-site ordered double-perovskite Sr2CoIrO6 thin films},
journal = {Physical Review B},
pages = {205121}
}

@article{10.1103/physreve.98.062109,
doi = {10.1103/physreve.98.062109},
url = {http://dx.doi.org/10.1103/physreve.98.062109},
year = 2018,
publisher = {American Physical Society ({APS})},
volume = {98},
author = {Richard L. C. Vink},
title = {Universality class of a displacive structural phase transition in two dimensions},
journal = {Physical Review E},
pages = {062109}
}

@article{10.1103/physrevb.98.195114,
doi = {10.1103/physrevb.98.195114},
url = {http://dx.doi.org/10.1103/physrevb.98.195114},
year = 2018,
publisher = {American Physical Society ({APS})},
volume = {98},
author = {P. Thiessen and V. Roddatis and F. Rieger and A. Belenchuk and M. Keunecke and V. Moshnyaga and Ch. Jooss},
title = {Effect of charge ordering on crossplane thermal conductivity in correlated perovskite oxide superlattices},
journal = {Physical Review B},
pages = {195114}
}

@article{10.1063/1.5025491,
doi = {10.1063/1.5025491},
url = {http://dx.doi.org/10.1063/1.5025491},
year = 2018,
publisher = {{AIP} Publishing},
volume = {123},
pages = {175108},
author = {F. Rieger and K. Kaiser and G. Bendt and V. Roddatis and P. Thiessen and S. Schulz and C. Jooss},
title = {Low intrinsic c-axis thermal conductivity in {Pvd} grown epitaxial Sb2Te3 films},
journal = {Journal of Applied Physics}
}

@article{10.1039/c7cp00198c,
doi = {10.1039/c7cp00198c},
url = {http://dx.doi.org/10.1039/c7cp00198c},
year = 2017,
publisher = {Royal Society of Chemistry ({RSC})},
volume = {19},
pages = {9762--9769},
author = {Johannes Martin and Melanie Gräf and Thilo Kramer and Christian Jooss and Min-Ju Choe and Katsuyo Thornton and Karl-Michael Weitzel},
title = {Charge attachment induced transport - bulk and grain boundary diffusion of potassium in {PrMnO}3},
journal = {Physical Chemistry Chemical Physics}
}

@article{10.1002/adsu.201700109,
doi = {10.1002/adsu.201700109},
url = {http://dx.doi.org/10.1002/adsu.201700109},
year = 2017,
publisher = {Wiley},
volume = {1},
pages = {1700109},
author = {Daniel Mierwaldt and Vladimir Roddatis and Marcel Risch and Julius Scholz and Janis Geppert and Majid Ebrahimizadeh Abrishami and Christian Jooss},
title = {Environmental {Tem} Investigation of Electrochemical Stability of Perovskite and Ruddlesden-Popper Type Manganite Oxygen Evolution Catalysts},
journal = {Advanced Sustainable Systems}
}

@article{10.1039/c6ee03046g,
doi = {10.1039/c6ee03046g},
url = {http://dx.doi.org/10.1039/c6ee03046g},
year = 2017,
publisher = {Royal Society of Chemistry ({RSC})},
volume = {10},
pages = {129--136},
author = {Joohyuk Park and Marcel Risch and Gyutae Nam and Minjoon Park and Tae Joo Shin and Suhyeon Park and Min Gyu Kim and Yang Shao-Horn and Jaephil Cho},
title = {Single crystalline pyrochlore nanoparticles with metallic conduction as efficient bi-functional oxygen electrocatalysts for Zn-air batteries},
journal = {Energy {\&} Environmental Science}
}

@article{10.1021/acscatal.7b01600,
doi = {10.1021/acscatal.7b01600},
url = {http://dx.doi.org/10.1021/acscatal.7b01600},
year = 2017,
publisher = {American Chemical Society ({ACS})},
volume = {7},
pages = {6843--6857},
author = {Joseph S. Elias and Kelsey A. Stoerzinger and Wesley T. Hong and Marcel Risch and Livia Giordano and Azzam N. Mansour and Yang Shao-Horn},
title = {In Situ Spectroscopy and Mechanistic Insights into {Co} Oxidation on Transition-Metal-Substituted Ceria Nanoparticles},
journal = {{ACS} Catalysis}
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