相间
锂(药物)
材料科学
离子
电压
纳米技术
光电子学
化学
电气工程
工程类
医学
遗传学
有机化学
生物
内分泌学
作者
Shihao Duan,Shuo‐Qing Zhang,Yong Li,Rui Guo,Ling Lv,Ruhong Li,Zunchun Wu,Menglu Li,Shunrui Xiao,Lixin Chen,Yong Shi,Tao Deng,Xiulin Fan
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2024-07-01
卷期号:9 (7): 3578-3586
被引量:16
标识
DOI:10.1021/acsenergylett.4c00917
摘要
The dehydrogenation of solvents presents a significant challenge at the cathode–electrolyte interface (CEI) in high-voltage lithium-ion batteries (LIBs), resulting in the generation of corrosive HF and posing detrimental effects on the sustainability of LIBs. Herein, we propose an interfacial self-enhanced strategy mediated by H-transfer to mitigate solvent dehydrogenation at the CEI. As a proof of concept, trimethyl phosphate (TMP) was coupled with 1,1,2,2,3,3,4-heptafluorocyclopentane (HFCP) to prepare the high-voltage electrolyte, where TMP serves to capture H free radicals produced by the dehydrogenation of HFCP, while the dehydrogenated-HFCP radicals would in situ passivate the cathode/electrolyte interface. The TMP/HFCP electrolyte enables a 4.4 V graphite||LiNi0.8Co0.1Mn0.1O2 LIB to achieve over 90% capacity retention after 1300 cycles at 0.5 C. Furthermore, the TMP/HFCP electrolyte exhibits favorable properties in terms of nonflammability and minimal gas production during electrochemical and thermal tests. This work presents a promising pathway for realizing high-voltage and high-safety LIBs.
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