电催化剂
材料科学
阳极
双金属片
催化作用
电化学
钝化
电化学能量转换
化学工程
纳米技术
电极
能量转换
异质结
储能
降级(电信)
电化学动力学
无机化学
动力学
过程(计算)
作者
Kexuan Liao,Tian-Zi Hao,Ruijin Meng,Yuanhui Zuo,Ting He,Lu Chen,Shuo Meng,Tingting Liu,Hang Lu,Chi Zhang,Jinhu Yang
标识
DOI:10.1002/adma.202511379
摘要
Abstract Catalysts are pivotal in enhancing reaction kinetics across various domains, including energy conversion and storage. However, their application in lithium‐ion batteries (LIBs) has been largely unexplored, primarily due to the challenges posed by solid‐solid conversion reactions in bulk electrode materials, and electrochemical instability and passivation of electrocatalysts during cycling. Herein, this study presents that Co atom clusters (Co ac ) cyclically regenerate from a designed heterostructure of bimetallic selenides anode (CoSe–ZnSe) during electrochemical lithiation process as a novel and effective solid‐state bulk‐phase electrocatalyst can significantly accelerate conversion reactions of ZnSe anode for fast‐charging LIBs. The propose strategy overcomes the bottlenecks in solid‐state bulk‐phase catalyst design, imparting Co ac catalyst with high catalytic efficiency, full‐voltage‐range electrochemical stability and anti‐passivation during long‐cycling test. With catalytic effect of Co ac , the batteries demonstrate fast‐charging performance such as unprecedented rate capability up to 50 A g −1 , as well as high‐rate long cyclability (3000 cycles at 10 A g −1 ).
科研通智能强力驱动
Strongly Powered by AbleSci AI