伏特
锂钴氧化物
电池(电)
电解质
材料科学
电极
电压
锂(药物)
氟化锂
能量密度
纳米技术
光电子学
化学工程
电气工程
化学
锂离子电池
工程物理
无机化学
物理
物理化学
工程类
功率(物理)
内分泌学
医学
量子力学
作者
Qi Xiong,Dedi Li,Shimei Li,Dechao Zhang,Ruhong Li,Shuo‐Qing Zhang,Shixun Wang,Hu Hong,Daming Zhu,Qi Liu,Xiulin Fan,Chunyi Zhi
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2025-09-17
卷期号:11 (38): eadx5020-eadx5020
标识
DOI:10.1126/sciadv.adx5020
摘要
Raising the charging voltage of a lithium||lithium cobalt oxide (Li||LiCoO 2 ) battery is a shortcut to realize high energy density in portable electronics, while the fragile interface of highly delithiated LiCoO 2 (>4.55 volts) can trigger the lattice oxygen release, thus leading to severe interfacial degradation and structural collapse. Here, using lithium pentadecafluorooctanoate as a fluorine source to build robust lithium fluoride–rich electrode-electrolyte interfaces, stable Li||LiCoO 2 batteries at high voltage have been realized, capable of cycling 1500, 600, and 188 times at 4.6, 4.7, and 4.8 volts, respectively. Furthermore, the practicality of Li||LiCoO 2 batteries at an unprecedented cutoff voltage of 4.8 volts has been validated by a 2.7–ampere hour pouch cell, which shows a superior energy density of 544 watt-hours per kilogram and can operate more than 50 cycles. Our exploration of 4.8-volt LiCoO 2 may pave the way to ceaselessly approach its theoretical capacity.
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