Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/87644
Title: The synergistic effect of cation mixing in mesoporous BixFe1−xVO4 heterojunction photoanodes for solar water splitting
Authors: Zhang, Mengyuan
Pham, Huu Khue
Fang, Yanan
Tay, Ying Fan
Fatwa F. Abdi
Wong, Lydia Helena
Keywords: Heterojunction
Photoactivity
Engineering::Materials
Issue Date: 2019
Source: Zhang, M., Pham, H. K., Fang, Y., Tay, Y. F., Fatwa F. Abdi, & Wong, L. H. (2019). The synergistic effect of cation mixing in mesoporous BixFe1−xVO4 heterojunction photoanodes for solar water splitting. Journal of Materials Chemistry A, 7(24), 14816-14824. doi:10.1039/C9TA01791G
Series/Report no.: Journal of Materials Chemistry A
Abstract: Mixed metal vanadates are an interesting class of materials due to their favorable bandgap for visible light absorption and their catalytic activity. Here, we report a novel BixFe1−xVO4 mixture system fabricated by electrospinning, which upon annealing is composed of triclinic FeVO4 and monoclinic BiVO4 phases. The mixture demonstrates extended optical absorption and a clear bandgap shift as compared with a pure BiVO4. This is also accompanied by an extended wavelength range for its photoactivity as evident from the incident photon-to-current efficiency. In addition, the mixture with a Bi/(Bi + Fe) ratio of 0.5 (i.e., x = 0.5) shows superior charge transfer and charge separation efficiency. The improved charge transfer efficiency is attributed to the higher catalytic activity of the mixed cation, while the presence of a BiVO4/FeVO4 heterojunction enhances the charge separation. The formation of the heterojunction is verified through detailed microscopic investigations revealing BiVO4 particles intimately surrounded by FeVO4. Our results demonstrate the advantage of establishing a mixture of complex metal oxides in extending optical absorption and boosting the photoelectrochemical performance.
URI: https://hdl.handle.net/10356/87644
http://hdl.handle.net/10220/49887
ISSN: 2050-7488
DOI: 10.1039/C9TA01791G
Rights: © 2019 The Royal Society of Chemistry. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence.
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:MSE Journal Articles

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