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Effect of Morphology and Manganese Valence on the Voltage Fade and Capacity Retention of Li[Li2/12Ni3/12Mn7/12]O2
Author(s) -
Michael G. Verde,
Haodong Liu,
Kyler J. Carroll,
Loïc Baggetto,
Gabriel M. Veith,
Ying Shirley Meng
Publication year - 2014
Publication title -
acs applied materials and interfaces
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.535
H-Index - 228
eISSN - 1944-8252
pISSN - 1944-8244
DOI - 10.1021/am504701s
Subject(s) - coprecipitation , x ray photoelectron spectroscopy , materials science , electrochemistry , valence (chemistry) , manganese , hydroxide , electrolyte , oxidation state , crystal structure , ion , cathode , chemical engineering , inorganic chemistry , analytical chemistry (journal) , electrode , chemistry , crystallography , metallurgy , engineering , chromatography , metal , organic chemistry
We have determined the electrochemical characteristics of the high voltage, high capacity Li-ion battery cathode material Li[Li2/12Ni3/12Mn7/12]O2 prepared using three different synthesis routes: sol-gel, hydroxide coprecipitation, and carbonate coprecipitation. Each route leads to distinct morphologies and surface areas while maintaining the same crystal structures. X-ray photoelectron spectroscopy (XPS) measurements reveal differences in their surface chemistries upon cycling, which correlate with voltage fading. Indeed, we observe the valence state of Mn on the surface to decrease upon lithiation, and this reduction is specifically correlated to discharging below 3.6 V. Furthermore, the data shows a correlation of the formation of Li2CO3 with the Mn oxidation state from the decomposition of electrolyte. These phenomena are related to each material's electrochemistry in order to expand upon the reaction mechanisms taking place-specifically in terms of the particle morphology produced by each synthetic approach.

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