成核
锂(药物)
化学工程
电解质
材料科学
阳极
阴极
纤维
碳纤维
电化学
氧气
基质(水族馆)
金属
电极
化学
复合材料
冶金
物理化学
有机化学
内分泌学
工程类
地质学
海洋学
复合数
医学
作者
Minjun Bae,Yonghwan Kim,Juhyung Choi,Seungman Park,Liwei Lin,tae-hyun yoo,Hwichan Hong,Dayun Jung,Yuanzhe Piao
出处
期刊:Carbon
[Elsevier BV]
日期:2022-05-20
卷期号:196: 663-675
被引量:13
标识
DOI:10.1016/j.carbon.2022.05.030
摘要
Lithium (Li) metal is the ultimate anode material for next generation batteries, thanks to its ultrahigh theoretical specific capacity and lowest reduction potential. However, an unstable solid electrolyte interphase caused by uneven Li deposition and infinite volume expansion of Li obstruct the commercialization of Li metal anodes. Herein, we introduce a unique strategy to tune lithiophobic carbon fiber (CF) to lithiophilic pore-gradient structured and oxygen-enriched carbon fiber (PGOCF) as dense Li nucleation enabler. The simultaneous regulation of surface chemistry and structure of CF is simply achieved by using CoAl layered double hydroxide as an etchant-protectant agent in thermal treatment, in which the porosifying role of Co and the protecting role of Al elements synergistically affect the morphology of PGOCF. The O enriched PGOCF (the atomic O ratio of 10.55%) can exhibit strong Li absorption, lowering Li nucleation barrier, and the pore-gradient structure of PGOCF can effectively lower Li nuclei-substrate contact angle, leading to dense and uniform Li electrodeposition. As a result, PGOCF exhibits an impressive electrochemical performance. When paired with a LiFePO4 cathode, [email protected] delivers a specific capacity of 138.3 mA h g−1 at 2C with an exceptional capacity retention of 98.3% for 500 cycles.
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