硫族元素
材料科学
原电池
欠电位沉积
Atom(片上系统)
过渡金属
催化作用
金属
贵金属
化学工程
化学物理
纳米技术
结晶学
化学
物理化学
电化学
冶金
嵌入式系统
循环伏安法
工程类
生物化学
计算机科学
电极
作者
Yi Shi,Wenguang Huang,Jian Li,Yue Zhou,Zhong‐Qiu Li,Yunchao Yin,Xing‐Hua Xia
标识
DOI:10.1038/s41467-020-18430-8
摘要
Abstract The growth of atomically dispersed metal catalysts (ADMCs) remains a great challenge owing to the thermodynamically driven atom aggregation. Here we report a surface-limited electrodeposition technique that uses site-specific substrates for the rapid and room-temperature synthesis of ADMCs. We obtained ADMCs by the underpotential deposition of a non-noble single-atom metal onto the chalcogen atoms of transition metal dichalcogenides and subsequent galvanic displacement with a more-noble single-atom metal. The site-specific electrodeposition enables the formation of energetically favorable metal–support bonds, and then automatically terminates the sequential formation of metallic bonding. The self-terminating effect restricts the metal deposition to the atomic scale. The modulated ADMCs exhibit remarkable activity and stability in the hydrogen evolution reaction compared to state-of-the-art single-atom electrocatalysts. We demonstrate that this methodology could be extended to the synthesis of a variety of ADMCs (Pt, Pd, Rh, Cu, Pb, Bi, and Sn), showing its general scope for functional ADMCs manufacturing in heterogeneous catalysis.
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