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Reversing the charge transfer between platinum and sulfur-doped carbon support for electrocatalytic hydrogen evolution

Open access
Yan, Qiang-Qiang, Wu, Dao-Xiong, Chu, Sheng-Qi, Chen, Zhi-Qin, Lin, Yue, Chen, Ming-Xi, Zhang, Jing, Wu, Xiao-Jun, Liang, Hai-Wei·2019·Nature Communications

Abstract

Metal–support interaction is of great significance for catalysis as it can induce charge transfer between metal and support, tame electronic structure of supported metals, impact adsorption energy of reaction intermediates, and eventually change the catalytic performance. Here, we report the metal size-dependent charge transfer reversal, that is, electrons transfer from platinum single atoms to sulfur-doped carbons and the carbon supports conversely donate electrons to Pt when their size is expanded to ~1.5 nm cluster. The electron-enriched Pt nanoclusters are far more active than electron-deficient Pt single atoms for catalyzing hydrogen evolution reaction, exhibiting only 11 mV overpotential at 10 mA cm−2 and a high mass activity of 26.1 A mg−1 at 20 mV, which is 38 times greater than that of commercial Pt/C. Our work manifests that the manipulation of metal size-dependent charge transfer between metal and support opens new avenues for developing high-active catalysts.

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Metadata

Authors
Yan, Q.-Q., Wu, D.-X., Chu, S.-Q., Chen, Z.-Q., Lin, Y., Chen, M.-X., Zhang, J., Wu, X.-J., & Liang, H.-W.
Venue
Nature Communications
Published
2019-10-31
Volume
10
Issue
1
Pages
4977-4977
ISSN
2041-1723 (ISSN-L)
OpenAlex
W2982521228
Cited by
444
References
16
FWCI
7.94
Type
journal article
Language
en
Open access
gold

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CoChat. (2026). Citation check: Reversing the charge transfer between platinum and sulfur-doped carbon support for electrocatalytic hydrogen evolution. https://app.cochat.ai/papers/10.1038/s41467-019-12851-w
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Yan, Q.-Q., Wu, D.-X., Chu, S.-Q., Chen, Z.-Q., Lin, Y., Chen, M.-X., Zhang, J., Wu, X.-J., & Liang, H.-W. (2019). Reversing the charge transfer between platinum and sulfur-doped carbon support for electrocatalytic hydrogen evolution. Nature Communications. https://doi.org/10.1038/s41467-019-12851-w

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