五氧化二铁
材料科学
钒
异质结
离子
光电子学
锂(药物)
纳米技术
无机化学
结晶学
化学工程
化学
冶金
有机化学
内分泌学
工程类
医学
作者
Henghan Dai,Xi Zhao,Hai Xu,Jia Yang,Jinyuan Zhou,Qiang Chen,Gengzhi Sun
出处
期刊:ACS Nano
[American Chemical Society]
日期:2022-04-15
卷期号:16 (4): 5556-5565
被引量:50
标识
DOI:10.1021/acsnano.1c10212
摘要
Designing a thick electrode with appropriate mass loading is a prerequisite toward practical applications for lithium ion batteries (LIBs) yet suffers severe limitations of slow electron/ion transport, unavoidable volume expansion, and the involvement of inactive additives, which lead to compromised output capacity, poor rate perforamnce, and cycling instability. Herein, self-supported thick electrode composed of vertically aligned two-dimensional (2D) heterostructures (V-MXene/V2O5) of rigid Ti3C2TX MXene and pliable vanadium pentoxide are assembled via an ice crystallization-induced strategy. The vertical channels prompt fast electron/ion transport within the entire electrode; in the meantime, the 3D MXene scaffold provides mechanical robustness during lithiation/delithiation. The optimized electrodes with 1 and 5 mg cm–2 of V-MXene/V2O5 respectively deliver 472 and 300 mAh g–1 at a current density of 0.2 A g–1, rate performance with 380 and 222 mAh g–1 retained at 5 A g–1, and reliability over 800 charge/discharge cycles.
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