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  Single-phase perovskite oxide with super-exchange induced atomic-scale synergistic active centers enables ultrafast hydrogen evolution

Dai, J., Zhu, Y., Tahini, H. A., Lin, Q., Chen, Y., Guan, D., et al. (2020). Single-phase perovskite oxide with super-exchange induced atomic-scale synergistic active centers enables ultrafast hydrogen evolution. Nature Communications, 11(1): 5657, pp. 1-10. doi:10.1038/s41467-020-19433-1.

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 Creators:
Dai, Jie1, Author
Zhu, Yinlong1, Author
Tahini, Hassan A.1, Author
Lin, Qian1, Author
Chen, Yu1, Author
Guan, Daqin1, Author
Zhou, Chuan1, Author
Hu, Zhiwei2, Author           
Lin, Hong-Ji1, Author
Chan, Ting-Shan1, Author
Chen, Chien-Te1, Author
Smith, Sean C.1, Author
Wang, Huanting1, Author
Zhou, Wei1, Author
Shao, Zongping1, Author
Affiliations:
1External Organizations, ou_persistent22              
2Zhiwei Hu, Physics of Correlated Matter, Max Planck Institute for Chemical Physics of Solids, Max Planck Society, ou_1863461              

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 Abstract: The state-of-the-art active HER catalysts in acid media (e.g., Pt) generally lose considerable catalytic performance in alkaline media mainly due to the additional water dissociation step. To address this issue, synergistic hybrid catalysts are always designed by coupling them with metal (hydro)oxides. However, such hybrid systems usually suffer from long reaction path, high cost and complex preparation methods. Here, we discover a single-phase HER catalyst, SrTi0.7Ru0.3O3-δ (STRO) perovskite oxide highlighted with an unusual super-exchange effect, which exhibits excellent HER performance in alkaline media via atomic-scale synergistic active centers. With insights from first-principles calculations, the intrinsically synergistic interplays between multiple active centers in STRO are uncovered to accurately catalyze different elementary steps of alkaline HER; namely, the Ti sites facilitates nearly-barrierless water dissociation, Ru sites function favorably for OH* desorption, and non-metal oxygen sites (i.e., oxygen vacancies/lattice oxygen) promotes optimal H* adsorption and H2 desorption. © 2020, The Author(s).

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Language(s): eng - English
 Dates: 2020-11-092020-11-09
 Publication Status: Issued
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 Identifiers: DOI: 10.1038/s41467-020-19433-1
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Title: Nature Communications
  Abbreviation : Nat. Commun.
Source Genre: Journal
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Publ. Info: London : Nature Publishing Group
Pages: - Volume / Issue: 11 (1) Sequence Number: 5657 Start / End Page: 1 - 10 Identifier: ISSN: 2041-1723
CoNE: https://pure.mpg.de/cone/journals/resource/2041-1723