Phase behavior and complex crystal structures of self-assembled tethered nanoparticle telechelics. Marson, R. L., Phillips, C. L., Anderson, J. A., & Glotzer, S. C. Nano Letters, 14(4):2071–2078, April, 2014. ISBN: 1530-6984
Phase behavior and complex crystal structures of self-assembled tethered nanoparticle telechelics [link]Paper  doi  abstract   bibtex   
Motivated by growing interest in the self-assembly of nanoparticles for applications such as photonics, organic photovoltaics, and DNA-assisted designer crystals, we explore the phase behavior of tethered spherical nanoparticles. Here, a polymer tether is used to geometrically constrain a pair of nanoparticles creating a tethered nanoparticle "telechelic". Using simulation, we examine how varying architectural features, such as the size ratio of the two end-group nanospheres and the length of the flexible tether, affects the self-assembled morphologies. We demonstrate not only that this hybrid building block maintains the same phase diversity as linear triblock copolymers, allowing for a variety of nanoparticle materials to replace polymer blocks, but also that new structures not previously reported are accessible. Our findings imply a robust underlying ordering mechanism is common among these systems, thus allowing flexibility in synthesis approaches to achieve a target morphology.
@article{Marson2014,
	title = {Phase behavior and complex crystal structures of self-assembled tethered nanoparticle telechelics},
	volume = {14},
	issn = {15306992},
	url = {http://pubs.acs.org/doi/abs/10.1021/nl500236b},
	doi = {10.1021/nl500236b},
	abstract = {Motivated by growing interest in the self-assembly of nanoparticles for applications such as photonics, organic photovoltaics, and DNA-assisted designer crystals, we explore the phase behavior of tethered spherical nanoparticles. Here, a polymer tether is used to geometrically constrain a pair of nanoparticles creating a tethered nanoparticle "telechelic". Using simulation, we examine how varying architectural features, such as the size ratio of the two end-group nanospheres and the length of the flexible tether, affects the self-assembled morphologies. We demonstrate not only that this hybrid building block maintains the same phase diversity as linear triblock copolymers, allowing for a variety of nanoparticle materials to replace polymer blocks, but also that new structures not previously reported are accessible. Our findings imply a robust underlying ordering mechanism is common among these systems, thus allowing flexibility in synthesis approaches to achieve a target morphology.},
	number = {4},
	urldate = {2014-05-13},
	journal = {Nano Letters},
	author = {Marson, Ryan L. and Phillips, Carolyn L. and Anderson, Joshua A. and Glotzer, Sharon C.},
	month = apr,
	year = {2014},
	pmid = {24641517},
	note = {ISBN: 1530-6984},
	keywords = {uses hoomd},
	pages = {2071--2078},
}

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