尖晶石
电解质
化学计量学
溶解
水溶液
钴
材料科学
无机化学
锂(药物)
锂钴氧化物
阴极
氧化物
化学
电池(电)
锂离子电池
电极
冶金
物理化学
功率(物理)
内分泌学
物理
医学
量子力学
作者
Hyeon Jeong Lee,Jihoon Lee,In Hyuk Son,Sangil Han,Pilgyu Byeon,Min Park,Sung‐Yoon Chung,Jang Wook Choi
标识
DOI:10.1021/acsaem.8b01317
摘要
Despite the long history in commercial lithium-ion batteries, layered lithium cobalt oxide (LiCoO2) suffers from structural degradations that shorten the cycle life when operating at high voltages (i.e., 4.5 V vs Li/Li+) in nonaqueous electrolytes or even at moderate voltages in aqueous electrolytes. This limited performance originates from the O3-to-O1 phase transition involving cobalt dissolution or the leaching of Li2O. Here, we report a one-pot synthesis that yields LiCoO2 bearing a spinel-Co3O4 surface structure with a thickness of 2 nm via lithium-deficient stoichiometry (Li:Co = 0.98:1). The lithium-deficiency induces the spinel structure, a thermodynamically preferred phase at the given stoichiometry, by temperature-specific phase separation. The spinel surface layer mitigates cobalt dissolution and oxygen gas evolution or avoids direct contact with the electrolyte causing the leaching of Li2O, improving the cyclability in nonaqueous and aqueous electrolytes by 35% and 20% after 100 cycles compared to that of LiCoO2 when the upper cutoff voltages were imposed at 4.5 V (vs Li/Li+) and 0.8 V (vs Ag/AgCl), respectively.
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