General synthesis and definitive structural identification of MN4C4 single-atom catalysts with tunable electrocatalytic activities

催化作用 合理设计 石墨烯 电化学 过渡金属 部分 组合化学 材料科学 纳米技术 密度泛函理论 Atom(片上系统) 化学 计算机科学 无机化学 计算化学 物理化学 嵌入式系统 有机化学 电极 立体化学
作者
Huilong Fei,Juncai Dong,Yexin Feng,Christopher S. Allen,Chengzhang Wan,Boris Volosskiy,Mufan Li,Zipeng Zhao,Yiliu Wang,Hongtao Sun,Pengfei An,Wenxing Chen,Zhiying Guo,Chain Lee,Dongliang Chen,Imran Shakir,Mingjie Liu,Tiandou Hu,Yadong Li,Angus I. Kirkland
出处
期刊:Nature Catalysis [Nature Portfolio]
卷期号:1 (1): 63-72 被引量:1963
标识
DOI:10.1038/s41929-017-0008-y
摘要

Single-atom catalysts (SACs) have recently attracted broad research interest as they combine the merits of both homogeneous and heterogeneous catalysts. Rational design and synthesis of SACs are of immense significance but have so far been plagued by the lack of a definitive correlation between structure and catalytic properties. Here, we report a general approach to a series of monodispersed atomic transition metals (for example, Fe, Co, Ni) embedded in nitrogen-doped graphene with a common MN4C4 moiety, identified by systematic X-ray absorption fine structure analyses and direct transmission electron microscopy imaging. The unambiguous structure determination allows density functional theoretical prediction of MN4C4 moieties as efficient oxygen evolution catalysts with activities following the trend Ni > Co > Fe, which is confirmed by electrochemical measurements. Determination of atomistic structure and its correlation with catalytic properties represents a critical step towards the rational design and synthesis of precious or nonprecious SACs with exceptional atom utilization efficiency and catalytic activities. Atomically dispersed metal catalysts are of increasing importance in many catalytic processes, but clear structural identification is challenging. Here, a general synthesis of metal (nickel, iron and cobalt) single-atom catalysts on nitrogen-doped graphene allows the authors to identify a common structure and furthermore correlate structure with electrocatalytic activity.
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