电负性
催化作用
合理设计
石墨烯
金属
电化学
吡咯
Atom(片上系统)
组合化学
纳米技术
化学
材料科学
计算机科学
物理化学
嵌入式系统
有机化学
电极
作者
Haoxiang Xu,Daojian Cheng,Dapeng Cao,Xiao Cheng Zeng
出处
期刊:Nature Catalysis
[Springer Nature]
日期:2018-04-27
卷期号:1 (5): 339-348
被引量:1405
标识
DOI:10.1038/s41929-018-0063-z
摘要
Developing highly active single-atom catalysts for electrochemical reactions is a key to future renewable energy technology. Here we present a universal design principle to evaluate the activity of graphene-based single-atom catalysts towards the oxygen reduction, oxygen evolution and hydrogen evolution reactions. Our results indicate that the catalytic activity of single-atom catalysts is highly correlated with the local environment of the metal centre, namely its coordination number and electronegativity and the electronegativity of the nearest neighbour atoms, validated by available experimental data. More importantly, we reveal that this design principle can be extended to metal–macrocycle complexes. The principle not only offers a strategy to design highly active nonprecious metal single-atom catalysts with specific active centres, for example, Fe-pyridine/pyrrole-N4 for the oxygen reduction reaction; Co-pyrrole-N4 for the oxygen evolution reaction; and Mn-pyrrole-N4 for the hydrogen evolution reaction to replace precious Pt/Ir/Ru-based catalysts, but also suggests that macrocyclic metal complexes could be used as an alternative to graphene-based single-atom catalysts.
科研通智能强力驱动
Strongly Powered by AbleSci AI