Single Carbon Vacancy Traps Atomic Platinum for Hydrogen Evolution Catalysis
Open accessAbstract
The coordinated configuration of atomic platinum (Pt) has always been identified as an active site with high intrinsic activity for hydrogen evolution reaction (HER). Herein, we purposely synthesize single vacancies in a carbon matrix (defective graphene) that can trap atomic Pt to form the Pt-C 3 configuration, which gives exceptionally high reactivity for HER in both acidic and alkaline solutions. The intrinsic activity of Pt-C 3 site is valued with a turnover frequency (TOF) of 26.41 s -1 and mass activity of 26.05 A g -1 at 100 mV, respectively, which are both nearly 18 times higher than those of commercial 20 wt % Pt/C. It is revealed that the optimal coordination Pt-C 3 has a stronger electron-capture ability and lower Gibbs free energy difference (Δ G ), resulting in promoting the reduction of adsorbed H + and the acceleration of H 2 desorption, thus exhibiting the extraordinary HER activity. This work provides a new insight on the unique coordinated configuration of dispersive atomic Pt in defective C matrix for superior HER performance.
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The small and homogeneous size of Pt nanoparticles loaded on the carbon aerogel facilitates charge transfer.
“This may be due to the small and homogeneous size of Pt NPs loaded on the CG, which have a good facilitation effect on charge transfer”
From Carbon Aerogels Loaded with Noble Metal Nanocrystal Electrocatalysts for Efficient Full Water Splitting (2023) · cites this paper as [51]
Pt-GA-2 TOF at 50 mV is ca. 6.56 times higher than commercial Pt/C.
“the TOF values of Pt-GA-2 at 50 and 100 mV are ca. 6.56 and 6.76 times higher compared with commercial Pt/C”
From Synergistic interaction of monodisperse Pt nanoparticles with defect‐rich graphene aerogel for efficient acidic hydrogen evolution (2025) · cites this paper as [44]
Cites
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- Authors
- Yang, Q., Liu, H., Yuan, P., Jia, Y., Zhuang, L., Zhang, H., Yan, X., Liu, G., Zhao, Y., Liu, J., Wei, S., Song, L., Wu, Q., Ge, B., Zhang, L., Wang, K., Wang, X., Chang, C.-R., & Yao, X.
- Affiliations
- Griffith University (AU)
- Xi'an Jiaotong University (CN)
- Fuzhou University (CN)
- East China University of Science and Technology (CN)
- State Key Laboratory of Chemical Resource Engineering (CN)
- Nanjing University of Science and Technology (CN)
- University of Science and Technology of China (CN)
- Zhejiang University of Technology (CN)
- Corresponding author
- Yuan, Pei
- Chang, Chun-Ran
- Yao, Xiangdong
- ORCID
- Venue
- Journal of the American Chemical Society
- Publisher
- American Chemical Society (ACS)
- Published
- 2022-01-07
- Volume
- 144
- Issue
- 5
- Pages
- 2171-2178
- ISSN
- 0002-7863 (ISSN-L)
- 1520-5126
- OpenAlex
- W4206378201
- Cited by
- 351
- References
- 1
- Citations by year
- 2026: 43 · 2025: 90 · 2024: 93 · 2023: 85 · 2022: 40
- FWCI
- 13.87
- Type
- journal article
- Language
- en
- Open access
- green
- hdl.handle.net
- Licence
- Locations
- Journal of the American Chemical Society (publishedVersion)
- PubMed (publishedVersion)
- Griffith Research Online (submittedVersion, other-oa)
- Funders
- Natural Science Foundation of Fujian Province (2021J02009)
- Australian Research Council (DE180101030, DP200103043)
- National Natural Science Foundation of China (22078064)
- Topics
- Physical Sciences › Energy › Renewable Energy, Sustainability and the Environment › Electrocatalysts for Energy Conversion
- Physical Sciences › Materials Science › Materials Chemistry › Hydrogen Storage and Materials
- Physical Sciences › Energy › Renewable Energy, Sustainability and the Environment › CO2 Reduction Techniques and Catalysts
- Keywords
- hydrogen evolution reaction, carbon vacancies, defective graphene, single-atom catalysts, electrocatalysis, acidic and alkaline electrolytes, electron capture, hydrogen desorption, turnover frequency, mass activity
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