4.7 Article

Novel 0D/1D ZnBi2O4/ZnO S-scheme photocatalyst for hydrogen production and BPA removal

期刊

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
卷 46, 期 47, 页码 24094-24106

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2021.04.208

关键词

ZnO; ZnBi2O4; S-scheme mechanism; Heterojunction; Dual-function photocatalyst; Hydrogen production

资金

  1. National Natural Science Foundation of China [52072241, 51772187]
  2. Shanghai Science and Technology Committee [18JC1410500]
  3. State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, Donghua University

向作者/读者索取更多资源

Developing interfacial connections between ZnO nanorods and ZnBi2O4 nanoparticles has successfully improved photocatalytic activity. The highest H-2 production was achieved with the ZnO-20 wt% ZnBi2O4 sample, showing a 12.7 times enhancement compared to pure ZnO.
Developing interfacial connections is one of the breakthrough strategies to improve the photocatalytic activity. Herein, ZnBi2O4 nanoparticles-ZnO nanorods heterojunction was successfully synthesized and used, as a dual-function photocatalyst, for photocatalytic degradation of Bisphenol A and hydrogen production with improved photocatalytic activity under simulated sunlight irradiation. The highest H-2 production (3.44 mmol g(-1) h(-1)) was obtained for ZnO-20 wt% ZnBi2O4 sample, which is around 12.7 times higher than pure ZnO. According to the HRTEM result, the intimate interfacial connections are formed between ZnO and ZnBi2O4 which could act as trapping centers for charge carriers and results in the boosted photocatalytic activity. Further, a high aspect ratio of 1D ZnO nanorods and small size of 0D ZnBi2O4 nanoparticles (similar to 10 nm) increases the number of interfacial contacts and thus the charge carriers' recombination was suppressed more efficiently. Based on the trapping experiments, ESR and Mott-Schottky analysis, ZnBi2O4-ZnO hybrid photocatalyst followed the S-scheme charge transfer mechanism. (C) 2021 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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