阳极
纳米复合材料
材料科学
电极
硫化物
化学工程
复合数
纳米技术
壳体(结构)
离子
复合材料
化学
冶金
物理化学
工程类
有机化学
作者
Run-Hang Chen,Ji-Miao Xiao,Ningning Zhu,R XIAO,Wanyi Liu,Xian Zeng,Yanfei Chen,Zi-Jian Yi,Guo-Yu Zhu,Lin Liu,De‐Shan Bin,Dan Li
标识
DOI:10.1002/anie.202402497
摘要
The large size of K‐ion makes the pursuit of stable high‐capacity anodes for K‐ion batteries (KIBs) a formidable challenge, particularly for high temperature KIBs as the electrode instability becomes more aggravated with temperature climbing. Herein, we demonstrate that a hollow ZnS@C nanocomposite (h‐ZnS@C) with a precise shell modulation can resist electrode disintegration to enable stable high‐capacity potassium storage at room and high temperature. Based on a model electrode, we identify an interesting structure‐function correlation of the h‐ZnS@C: with an increase in the shell thickness, the cyclability increases while the rate and capacity decreases, shedding light on the design of high‐performance h‐ZnS@C anodes via engineering the shell thickness. Typically, the h‐ZnS@C anode with a shell thickness of 60 nm can deliver an impressive comprehensive performance at room temperature; the h‐ZnS@C with shell thickness increasing to 75 nm can achieve an extraordinary stability (88.6% capacity retention over 450 cycles) with a high capacity (450 mAh g‐1) and a superb rate even at an extreme temperature of 60 ℃, which is much superior than those reported anodes. This contribution envisions new perspectives on rational design of functional metal sulfides composite toward high‐performance KIBs with insights into the significant structure‐function correlation.
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