电催化剂
酞菁
催化作用
石墨烯
化学
色散(光学)
选择性
基质(水族馆)
组合化学
氧化物
分子
密度泛函理论
无机化学
纳米技术
材料科学
化学工程
有机化学
电化学
计算化学
电极
物理化学
海洋学
工程类
地质学
物理
光学
作者
Yi Qin,Cheng‐Hao Chuang,Xiaojing Liu,Xian Liang,Linfeng Xie,Kuan Wang,Chih‐Wen Pao,Ying‐Rui Lu,Yang Liu,Yawei Chen,Zhanwu Lei,Pengfei Yan,Liang Wu,Shuhong Jiao,Qing Li,Ruiguo Cao
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2024-04-30
卷期号:14 (10): 7514-7525
被引量:7
标识
DOI:10.1021/acscatal.4c00795
摘要
Molecular catalysts have attracted significant attention because of their high activity, selectivity, and tunability. However, in heterogeneous catalysis, the uniform dispersion and immobilization of molecular catalysts on the supporting substrate remain a significant challenge due to their aggregation tendency. Here, we present a facile strategy to molecularly disperse and immobilize a series of macrocyclic metal complexes onto reduced graphene oxide (rGO) by using DNA as a mediator. The electroactive amounts of molecularly dispersed iron phthalocyanine (FePc) molecules are increased by ∼50 times greater than that of pristine FePc catalyst. As a result, the single-molecule catalyst demonstrates a notable power density (∼290 mW cm–2) in an H2/O2 alkaline polymer electrolyte fuel cell. Operando X-ray absorption spectroscopy experiments combined with density functional theory calculations reveal that the coordination interaction between FePc and DNA enables the molecular dispersion and immobilization of FePc on the surface of rGO, and consequently improves the activity by regulating the electronic structure of active centers. This study points out a facile strategy to tackle the fundamental challenges facing molecular catalysts in long-lasting energy conversion technologies.
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