Highly Efficient Photocatalytic Hydrogen Evolution by ReS2 via a Two-Electron Catalytic Reaction

© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Bibliographische Detailangaben
Veröffentlicht in:Advanced materials (Deerfield Beach, Fla.). - 1998. - 30(2018), 23 vom: 10. Juni, Seite e1707123
1. Verfasser: Zhang, Qin (VerfasserIn)
Weitere Verfasser: Wang, Wenjie, Zhang, Jiaqian, Zhu, Xiaohui, Zhang, Qiqi, Zhang, Yujing, Ren, Zemian, Song, Shuaishuai, Wang, Jinming, Ying, Zihao, Wang, Rui, Qiu, Xiaohui, Peng, Tianyou, Fu, Lei
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2018
Zugriff auf das übergeordnete Werk:Advanced materials (Deerfield Beach, Fla.)
Schlagworte:Journal Article ReS2 hydrogen evolution trion two-electron catalytic reaction
Beschreibung
Zusammenfassung:© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Highly efficient photocatalytic hydrogen evolution (PHE) is highly desirable for addressing the global energy crisis and environmental problems. Although much attention has been given to electron-hole separation, ridding photocatalysts of poor efficiency remains challenging. Here, a two-electron catalytic reaction is developed by utilizing the distinct trion behavior of ReS2 and the efficient reduction of two H+ (2H+ + 2e- → H2 ) is realized. Due to the monolayer-like structure of the catalyst, the free electrons in ReS2 can be captured by the tightly bound excitons to form trions consisting of two electrons and one hole. These trions can migrate to the surface and participate in the two-electron reaction at the abundant active sites. As expected, such a two-electron catalytic reaction endows ReS2 with a PHE rate of 13 mmol g-1 h-1 under visible light irradiation. Meanwhile, this reaction allows the typically poor PHE efficiency of pure transition metal dichalcogenides to be overcome. The proposed two-electron catalytic reaction provides a new approach to the design of photocatalysts for PHE
Beschreibung:Date Completed 01.08.2018
Date Revised 01.10.2020
published: Print-Electronic
Citation Status PubMed-not-MEDLINE
ISSN:1521-4095
DOI:10.1002/adma.201707123