Site-specific electrodeposition enables self-terminating growth of atomically dispersed metal catalysts

被引:171
作者
Shi, Yi [1 ]
Huang, Wen-Mao [1 ]
Li, Jian [1 ]
Zhou, Yue [1 ]
Li, Zhong-Qiu [1 ]
Yin, Yun-Chao [1 ]
Xia, Xing-Hua [1 ]
机构
[1] Nanjing Univ, Sch Chem & Chem Engn, State Key Lab Analyt Chem Life Sci, Nanjing 210023, Peoples R China
基金
中国国家自然科学基金;
关键词
SINGLE-ATOM CATALYSTS; HYDROGEN EVOLUTION; PLATINUM; MOS2; DEPOSITION; SURFACE; CARBON;
D O I
10.1038/s41467-020-18430-8
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 roomtemperature 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.
引用
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页数:9
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