Affiliation:
1. Shenzhen Geim Graphene Center Institute of Materials Research Tsinghua Shenzhen International Graduate School Tsinghua University Shenzhen 518055 China
2. State Key Laboratory of Coal Combustion School of Energy and Power Engineering Huazhong University of Science and Technology (HUST) Wuhan 430074 China
Abstract
AbstractVarious electrolyte additives are developed to construct a cathode electrolyte interphase (CEI) layer for high‐voltage LiCoO2 since the cathode suffers severe interfacial degradation when increasing the cut‐off voltage over 4.55 V. However, the CEI derived from the additive sacrificial reaction faces the risk of rupture due to the corrosion reaction and the volumetric variation of the cathode. Herein, a non‐passivating cathode interface is realized for 4.6 V LiCoO2 with a non‐sacrificial electrolyte additive (TBAClO4) by regulating the solvent environment at the interface rather than the preferential decomposition for CEI formation. Owing to the novel protection mechanism, the cell performance shows little dependence on the CEI‐formation process. Therefore, an ultra‐high initial coulombic efficiency (96.63%) and excellent cycling stability (81% capacity retention after 300 cycles) are achieved in Li||LiCoO2 batteries. Moreover, even with the electrolyte containing 1000 ppm H2O, the remarkable water capture ability of the additive together with its interfacial regulation enables the 4.6 V Li||LiCoO2 battery to retain 80% capacity after 200 cycles. This non‐sacrificial strategy provides new insights into high‐voltage electrolyte additive design for high‐energy‐density lithium metal batteries.
Funder
National Basic Research Program of China
National Natural Science Foundation of China
Cited by
8 articles.
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