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Anchoring zero valence single atoms of nickel and iron on graphdiyne for hydrogen evolution

Yurui XueKey Laboratory of Organic Solids, Institute of Chemistry, The Chinese Academy of Sciences, Beijing, 100190, PR ChinaBolong HuangDepartment of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University-Hung Hom, Kowloon, Hong Kong SAR, ChinaYuanping YiKey Laboratory of Organic Solids, Institute of Chemistry, The Chinese Academy of Sciences, Beijing, 100190, PR ChinaYuan GuoKey Laboratory of Organic Solids, Institute of Chemistry, The Chinese Academy of Sciences, Beijing, 100190, PR ChinaZicheng ZuoKey Laboratory of Organic Solids, Institute of Chemistry, The Chinese Academy of Sciences, Beijing, 100190, PR ChinaYongjun LiKey Laboratory of Organic Solids, Institute of Chemistry, The Chinese Academy of Sciences, Beijing, 100190, PR ChinaZhiyu JiaKey Laboratory of Organic Solids, Institute of Chemistry, The Chinese Academy of Sciences, Beijing, 100190, PR ChinaHuibiao LiuKey Laboratory of Organic Solids, Institute of Chemistry, The Chinese Academy of Sciences, Beijing, 100190, PR ChinaYuliang LiKey Laboratory of Organic Solids, Institute of Chemistry, The Chinese Academy of Sciences, Beijing, 100190, PR China
2018en
ABI

Annotatsiya

Electrocatalysis by atomic catalysts is a major focus of chemical and energy conversion effort. Although transition-metal-based bulk electrocatalysts for electrochemical application on energy conversion processes have been reported frequently, anchoring the stable transition-metal atoms (e.g. nickel and iron) still remains a practical challenge. Here we report a strategy for fabrication of ACs comprising only isolated nickel/iron atoms anchored on graphdiyne. Our findings identify the very narrow size distributions of both nickel (1.23 Å) and iron (1.02 Å), typical sizes of single-atom nickel and iron. The precision of this method motivates us to develop a general approach in the field of single-atom transition-metal catalysis. Such atomic catalysts have high catalytic activity and stability for hydrogen evolution reactions.

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