| Literature DB >> 31141374 |
Laura Simonelli1, Andrea Sorrentino1, Carlo Marini1, Nitya Ramanan1, Dominique Heinis1, Wojciech Olszewski1,2, Angelo Mullaliu3, Agnese Birrozzi4,5, Nina Laszczynski4,5, Marco Giorgetti6, Stefano Passerini4,5, Dino Tonti7.
Abstract
Lithium-rich transition-metal-oxide cathodes are among the most promising materials for next generation lithium-ion-batteries because they operate at high voltages and deliver high capacities. However, their cycle-life remains limited, and individual roles of the transition-metals are still not fully understood. Using bulk-sensitive X-ray absorption and emission spectroscopy on Li[Li0.2Ni0.16Mn0.56Co0.08]O2, we inspect the behavior of Mn, generally considered inert upon the electrochemical process. During the first charge Mn appears to be redox-active showing a partial transformation from high-spin Mn4+ to Mn3+ in both high and low spin configurations, where the latter is expected to favor reversible cycling. The Mn redox-state with cycling continues changing in opposition to the expected charge compensation and is correlated with Ni oxidation/reduction, also spatially. The findings suggest that strain induced on the Mn-O sublattice by Ni oxidation triggers Mn reduction. These results unravel the Mn role in controlling the electrochemistry of Li-rich cathodes.Entities:
Year: 2019 PMID: 31141374 DOI: 10.1021/acs.jpclett.9b01174
Source DB: PubMed Journal: J Phys Chem Lett ISSN: 1948-7185 Impact factor: 6.475