Reaction Heterogeneity in LiNi$_{\textrm{0.8}}$Co$_{\textrm{0.15}}$Al$_{\textrm{0.05}}$O$_{\textrm{2}}$ Induced by Surface Layer. Grenier, A., Liu, H., Wiaderek, K., Lebens-Higgins, Z., Borkiewicz, O., Piper, L., Chupas, P., & Chapman, K. Chemistry of Materials, 29(17):7345 – 7352, August, 2017. doi abstract bibtex Through operando synchrotron powder X-ray diffraction (XRD) analysis of layered transition metal oxide electrodes of composition LiNi$_{\textrm{0.8}}$Co$_{\textrm{0.15}}$Al$_{\textrm{0.05}}$O$_{\textrm{2}}$ (NCA), we decouple the intrinsic bulk reaction mechanism from surface-induced effects. For identically prepared and cycled electrodes stored in different environments, we demonstrate that the intrinsic bulk reaction for pristine NCA follows solid-solution mechanism, not a two-phase as suggested previously. By combining high resolution powder X-ray diffraction, diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) and surface sensitive X-ray photoelectron spectroscopy (XPS), we demonstrate that adventitious Li$_{\textrm{2}}$CO$_{\textrm{3}}$ forms on the electrode particle surface during exposure to air, through reaction with atmospheric CO2. This surface impedes ionic and electronic transport to the underlying electrode, with progressive erosion of this layer during cycling giving rise to different reaction states in particles with an intact vs an eroded Li$_{\textrm{2}}$CO$_{\textrm{3}}$ surface-coating. This reaction heterogeneity, with a bimodal distribution of reaction states, has previously been interpreted as a “two-phase” reaction mechanism for NCA, as an activation step that only occurs during the first cycle. Similar surface layers may impact the reaction mechanism observed in other electrode materials using bulk probes such as operando powder XRD.
@article{grenier_reaction_2017,
title = {Reaction {Heterogeneity} in {LiNi}$_{\textrm{0.8}}${Co}$_{\textrm{0.15}}${Al}$_{\textrm{0.05}}${O}$_{\textrm{2}}$ {Induced} by {Surface} {Layer}},
volume = {29},
copyright = {All rights reserved},
issn = {0897-4756},
doi = {10.1021/acs.chemmater.7b02236},
abstract = {Through operando synchrotron powder X-ray diffraction (XRD) analysis of layered transition metal oxide electrodes of composition LiNi$_{\textrm{0.8}}$Co$_{\textrm{0.15}}$Al$_{\textrm{0.05}}$O$_{\textrm{2}}$ (NCA), we decouple the intrinsic bulk reaction mechanism from surface-induced effects. For identically prepared and cycled electrodes stored in different environments, we demonstrate that the intrinsic bulk reaction for pristine NCA follows solid-solution mechanism, not a two-phase as suggested previously. By combining high resolution powder X-ray diffraction, diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) and surface sensitive X-ray photoelectron spectroscopy (XPS), we demonstrate that adventitious Li$_{\textrm{2}}$CO$_{\textrm{3}}$ forms on the electrode particle surface during exposure to air, through reaction with atmospheric CO2. This surface impedes ionic and electronic transport to the underlying electrode, with progressive erosion of this layer during cycling giving rise to different reaction states in particles with an intact vs an eroded Li$_{\textrm{2}}$CO$_{\textrm{3}}$ surface-coating. This reaction heterogeneity, with a bimodal distribution of reaction states, has previously been interpreted as a “two-phase” reaction mechanism for NCA, as an activation step that only occurs during the first cycle. Similar surface layers may impact the reaction mechanism observed in other electrode materials using bulk probes such as operando powder XRD.},
number = {17},
journal = {Chemistry of Materials},
author = {Grenier, Antonin and Liu, Hao and Wiaderek, Kamila and Lebens-Higgins, Zachary and Borkiewicz, Olaf and Piper, Louis and Chupas, Peter and Chapman, Karena},
month = aug,
year = {2017},
pages = {7345 -- 7352},
}
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For identically prepared and cycled electrodes stored in different environments, we demonstrate that the intrinsic bulk reaction for pristine NCA follows solid-solution mechanism, not a two-phase as suggested previously. By combining high resolution powder X-ray diffraction, diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) and surface sensitive X-ray photoelectron spectroscopy (XPS), we demonstrate that adventitious Li$_{\\textrm{2}}$CO$_{\\textrm{3}}$ forms on the electrode particle surface during exposure to air, through reaction with atmospheric CO2. This surface impedes ionic and electronic transport to the underlying electrode, with progressive erosion of this layer during cycling giving rise to different reaction states in particles with an intact vs an eroded Li$_{\\textrm{2}}$CO$_{\\textrm{3}}$ surface-coating. This reaction heterogeneity, with a bimodal distribution of reaction states, has previously been interpreted as a “two-phase” reaction mechanism for NCA, as an activation step that only occurs during the first cycle. 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For identically prepared and cycled electrodes stored in different environments, we demonstrate that the intrinsic bulk reaction for pristine NCA follows solid-solution mechanism, not a two-phase as suggested previously. By combining high resolution powder X-ray diffraction, diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) and surface sensitive X-ray photoelectron spectroscopy (XPS), we demonstrate that adventitious Li$_{\\textrm{2}}$CO$_{\\textrm{3}}$ forms on the electrode particle surface during exposure to air, through reaction with atmospheric CO2. This surface impedes ionic and electronic transport to the underlying electrode, with progressive erosion of this layer during cycling giving rise to different reaction states in particles with an intact vs an eroded Li$_{\\textrm{2}}$CO$_{\\textrm{3}}$ surface-coating. 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