TY - JOUR
T1 - Regulating the Electron Distribution of Metal-Oxygen for Enhanced Oxygen Stability in Li-rich Layered Cathodes
AU - Yin, Zijia
AU - Zhao, Jun
AU - Luo, Dong
AU - Chin, Yi-Ying
AU - Chen, Chien-Te
AU - Chen, Huaican
AU - Yin, Wen
AU - Tang, Yu
AU - Yang, Tingting
AU - Ren, Jincan
AU - Li, Tianyi
AU - Wiaderek, Kamila M.
AU - Kong, Qingyu
AU - Fan, Jun
AU - Zhu, He
AU - Ren, Yang
AU - Liu, Qi
PY - 2024/6/26
Y1 - 2024/6/26
N2 - Li-rich Mn-based layered oxides (LLO) hold great promise as cathode materials for lithium-ion batteries (LIBs) due to their unique oxygen redox (OR) chemistry, which enables additional capacity. However, the LLOs face challenges related to the instability of their OR process due to the weak transition metal (TM)-oxygen bond, leading to oxygen loss and irreversible phase transition that results in severe capacity and voltage decay. Herein, a synergistic electronic regulation strategy of surface and interior structures to enhance oxygen stability is proposed. In the interior of the materials, the local electrons around TM and O atoms may be delocalized by surrounding Mo atoms, facilitating the formation of stronger TM─O bonds at high voltages. Besides, on the surface, the highly reactive O atoms with lone pairs of electrons are passivated by additional TM atoms, which provides a more stable TM─O framework. Hence, this strategy stabilizes the oxygen and hinders TM migration, which enhances the reversibility in structural evolution, leading to increased capacity and voltage retention. This work presents an efficient approach to enhance the performance of LLOs through surface-to-interior electronic structure modulation, while also contributing to a deeper understanding of their redox reaction. © 2024 The Authors. Advanced Science published by Wiley-VCH GmbH.
AB - Li-rich Mn-based layered oxides (LLO) hold great promise as cathode materials for lithium-ion batteries (LIBs) due to their unique oxygen redox (OR) chemistry, which enables additional capacity. However, the LLOs face challenges related to the instability of their OR process due to the weak transition metal (TM)-oxygen bond, leading to oxygen loss and irreversible phase transition that results in severe capacity and voltage decay. Herein, a synergistic electronic regulation strategy of surface and interior structures to enhance oxygen stability is proposed. In the interior of the materials, the local electrons around TM and O atoms may be delocalized by surrounding Mo atoms, facilitating the formation of stronger TM─O bonds at high voltages. Besides, on the surface, the highly reactive O atoms with lone pairs of electrons are passivated by additional TM atoms, which provides a more stable TM─O framework. Hence, this strategy stabilizes the oxygen and hinders TM migration, which enhances the reversibility in structural evolution, leading to increased capacity and voltage retention. This work presents an efficient approach to enhance the performance of LLOs through surface-to-interior electronic structure modulation, while also contributing to a deeper understanding of their redox reaction. © 2024 The Authors. Advanced Science published by Wiley-VCH GmbH.
KW - delocalized electrons
KW - electronic modulation
KW - in situ characterization
KW - lithium-rich oxide cathodes
KW - oxygen stability
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UR - https://www.scopus.com/record/pubmetrics.uri?eid=2-s2.0-85190873010&origin=recordpage
U2 - 10.1002/advs.202307397
DO - 10.1002/advs.202307397
M3 - RGC 21 - Publication in refereed journal
C2 - 38650173
SN - 2198-3844
VL - 11
JO - Advanced Science
JF - Advanced Science
IS - 24
M1 - 2307397
ER -