Decline Mechanism of Graphite/Lithium Metal Hybrid Anode and Its Stabilization by Inorganic-Rich Solid Electrolyte Interface

被引:4
|
作者
Wu, Zeyu [1 ]
Wang, Zhenhua [1 ]
Zhang, Jing [1 ]
Bai, Zhe [1 ]
Zhao, Lina [1 ]
Li, Ruilong [1 ]
Yang, Zhanfeng [1 ]
Bai, Yu [1 ]
Sun, Kening [1 ]
机构
[1] Beijing Inst Technol, Beijing Key Lab Chem Power Source & Green Catalysi, Beijing 100081, Peoples R China
基金
中国国家自然科学基金;
关键词
hybrid battery; graphite; lithium plating; anode stabilization; solid-electrolyte interphase; IN-SITU RAMAN; LITHIUM METAL; RELAXATION-TIMES; HIGH-ENERGY; SPECTROSCOPY; CHALLENGES; BATTERY; CARBON; INTERCALATION;
D O I
10.1021/acsami.3c05630
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Thegraphite/lithium metal hybrid anode shows great potential forachieving high-specific-energy lithium batteries. Despite the "deadlithium" problem caused by repeated stripping and depositionof Li component based on a conversion reaction, the degradation mechanism,based on intercalation reaction, of graphite in a hybrid anode isgenerally ignored. In this contribution, through in situ X-ray diffractionand in situ Raman analysis, we reveal that hysteresis and the mixed-phasestate of graphite during deintercalation play a critical role in hybridbattery degradation. On the other hand, we successfully mitigatedgraphite degradation and increased the reversible capacity of thehybrid anode by introducing an inorganic-rich solid electrolyte interface.Remarkably, the hybrid anode (30% higher specific capacity comparedto graphite) exhibits an average coulombic efficiency of 99.11% andretains 96.13% of initial capacity over 120 cycles. This work shedsnew light on the advancement of high-specific-energy lithium secondarybatteries.
引用
收藏
页码:34922 / 34930
页数:9
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