催化作用
氧化还原
电化学
化学
硫黄
纳米材料基催化剂
动力学
无机化学
电子转移
锂(药物)
电化学动力学
化学工程
材料科学
电极
光化学
有机化学
物理化学
物理
量子力学
工程类
医学
内分泌学
作者
Yunhan Xu,Wenkui Yuan,Chuannan Geng,Zhonghao Hu,Qiang Li,Yufei Zhao,Xu Zhang,Zhen Zhou,Chunpeng Yang,Quan‐Hong Yang
标识
DOI:10.1002/advs.202402497
摘要
Abstract Catalysis is crucial to improve redox kinetics in lithium–sulfur (Li–S) batteries. However, conventional catalysts that consist of a single metal element are incapable of accelerating stepwise sulfur redox reactions which involve 16‐electron transfer and multiple Li 2 S n (n = 2–8) intermediate species. To enable fast kinetics of Li–S batteries, it is proposed to use high‐entropy alloy (HEA) nanocatalysts, which are demonstrated effective to adsorb lithium polysulfides and accelerate their redox kinetics. The incorporation of multiple elements (Co, Ni, Fe, Pd, and V) within HEAs greatly enhances the catalytically active sites, which not only improves the rate capability, but also elevates the cycling stability of the assembled batteries. Consequently, HEA‐catalyzed Li–S batteries achieve a high capacity up to 1364 mAh g −1 at 0.1 C and experience only a slight capacity fading rate of 0.054% per cycle over 1000 cycles at 2 C, while the assembled pouch cell achieves a high specific capacity of 1192 mAh g −1 . The superior performance of Li–S batteries demonstrates the effectiveness of the HEA catalysts with maximized synergistic effect for accelerating S conversion reactions, which opens a way to catalytically improving stepwise electrochemical conversion reactions.
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