Affiliation:
1. School of Advanced Materials Peking University Shenzhen Graduate School Peking University Shenzhen Guangdong 518055 China
2. Tsinghua‐Berkeley Shenzhen Institute & Tsinghua Shenzhen International Graduate School Tsinghua University Shenzhen Guangdong 518055 China
3. Chemical Sciences and Engineering Division Argonne National Laboratory Lemont IL 60439 USA
4. School of Energy and Power Engineering Jiangsu University Zhenjiang Jiangsu 212013 China
5. Institute of Materials Research Tsinghua Shenzhen International Graduate School Tsinghua University Shenzhen Guangdong 518055 China
Abstract
AbstractFor LiCoO2 (LCO) operated beyond 4.55 V (vs Li/Li+), it usually suffers from severe surface degradation. Constructing a robust cathode/electrolyte interphase (CEI) is effective to alleviate the above issues, however, the correlated mechanisms still remain vague. Herein, a progressively reinforced CEI is realized via constructing Zr─O deposits (ZrO2 and Li2ZrO3) on LCO surface (i.e., Z‐LCO). Upon cycle, these Zr─O deposits can promote the decomposition of LiPF6, and progressively convert to the highly dispersed Zr─O─F species. In particular, the chemical reaction between LiF and Zr─O─F species further leads to the densification of CEI, which greatly reinforces its toughness and conductivity. Combining the robust CEI and thin surface rock‐salt layer of Z‐LCO, several benefits are achieved, including stabilizing the surface lattice oxygen, facilitating the interface Li+ transport kinetics, and enhancing the reversibility of O3/H1‐3 phase transition, etc. As a result, the Z‐LCO||Li cells exhibit a high capacity retention of 84.2% after 1000 cycles in 3–4.65 V, 80.9% after 1500 cycles in 3–4.6 V, and a high rate capacity of 160 mAh g−1 at 16 C (1 C = 200 mA g−1). This work provides a new insight for developing advanced LCO cathodes.
Funder
Basic and Applied Basic Research Foundation of Guangdong Province