材料科学
镍
阴极
催化作用
电池(电)
二茂铁
金属
化学工程
无机化学
电化学
冶金
电极
纳米技术
有机化学
电气工程
物理化学
功率(物理)
化学
物理
量子力学
工程类
作者
Haixia Chen,Xijuan Li,Z. Liu,Yunyun Xu,Yige Yan,Peng Li,Kun Chang,Xianli Huang,Jianping He,Tao Wang
标识
DOI:10.1002/adfm.202412387
摘要
Abstract Li‐CO 2 batteries, as a novel type of secondary battery, show great potential for energy conversion and storage. However, challenges such as large electrode polarization and poor cycling performance, stemming from difficulties in decomposing discharge products, limit their practical application. Here, Ferrocene‐based nickel metal–organic framework (Ni‐Fc) nanosheets structure to act as cathode catalysts, prepared via a one‐pot solvothermal reaction. X‐ray absorption fine structure (XAFS) analysis shows that Ni metal forms abundant catalytic active centers with O coordination of carboxylic acid groups in ferrocene units. The Ni‐Fc‐based battery demonstrates a high discharge capacity of 18636 mAh g −1 and exhibits a cycle life exceeding 2000 h at a current of 200 mA g −1 . Density functional theory (DFT) calculations indicate that the stronger interaction of Ni‐Fc with discharge intermediates and enhanced Li adsorption accelerate battery reaction kinetics. This study introduces novel catalyst design concepts aimed at achieving high‐performance CO 2 reduction and oxidation, thereby advancing Li‐CO 2 batteries toward practical application.
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