材料科学
锂(药物)
电解质
钴
锂钴氧化物
化学工程
自放电
石墨
二甲氧基乙烷
电池(电)
无机化学
锂离子电池
离子
电极
有机化学
电化学
冶金
复合材料
化学
物理化学
医学
量子力学
物理
功率(物理)
内分泌学
工程类
作者
Hao Jia,Xianhui Zhang,Yaobin Xu,Lianfeng Zou,Ju‐Myung Kim,Peiyuan Gao,Mark Engelhard,Qiuyan Li,Chaojiang Niu,Bethany E. Matthews,Teresa Lemmon,Jiangtao Hu,Chongmin Wang,Wu Xu
标识
DOI:10.1021/acsami.1c12072
摘要
The criticality of cobalt (Co) has been motivating the quest for Co-free positive electrode materials for building lithium (Li)-ion batteries (LIBs). However, the LIBs based on Co-free positive electrode materials usually suffer from relatively fast capacity decay when coupled with conventional LiPF6-organocarbonate electrolytes. To address this issue, a 1,2-dimethoxyethane-based localized high-concentration electrolyte (LHCE) was developed and evaluated in a Co-free Li-ion cell chemistry (graphite||LiNi0.96Mg0.02Ti0.02O2). Extraordinary capacity retentions were achieved with the LHCE in coin cells (95.3%), single-layer pouch cells (79.4%), and high-capacity loading double-layer pouch cells (70.9%) after being operated within the voltage range of 2.5–4.4 V for 500 charge/discharge cycles. The capacity retentions of counterpart cells using the LiPF6-based conventional electrolyte only reached 61.1, 57.2, and 59.8%, respectively. Mechanistic studies reveal that the superior electrode/electrolyte interphases formed by the LHCE and the intrinsic chemical stability of the LHCE account for the excellent electrochemical performance in the Co-free Li-ion cells.
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