噻吩
电催化剂
电化学
杂原子
硫黄
催化作用
化学
共价键
阴极
铂金
共价有机骨架
电子转移
组合化学
氧还原反应
化学工程
无机化学
光化学
有机化学
电极
物理化学
工程类
戒指(化学)
作者
Shunkai Chang,Cuiyan Li,Hui Li,Liangkui Zhu,Qianrong Fang
标识
DOI:10.1007/s40242-022-1465-7
摘要
Exploring novel materials deriving from earth resources to substitute for platinum(Pt) electrocatalyst to promote oxygen reduction reaction(ORR) of fuel cell cathode is very important. Herein, we have exploited two crystallographic thiophene-sulfur covalent organic frameworks(COFs), termed JUC-607 and JUC-608, as electrocatalysts that exhibited good ORR performances. These thiophene-sulfur COFs exhibited high stability, and their functional groups acting as active centers in the ORR can be precisely determined. Notably, due to a larger aperture for mass transfer and electrons transport, JUC-608 displayed a growing electrochemical performance, leading to a better ORR activity. Thus, this study will provide a new strategy for designing heteroatom-based COF materials for high-performance electrochemical catalysis.
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