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


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.

SUBMITTER: Shi Y 

PROVIDER: S-EPMC7486907 | biostudies-literature | 2020 Sep

REPOSITORIES: biostudies-literature

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

Shi Yi Y   Huang Wen-Mao WM   Li Jian J   Zhou Yue Y   Li Zhong-Qiu ZQ   Yin Yun-Chao YC   Xia Xing-Hua XH  

Nature communications 20200911 1


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-a  ...[more]

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