Electrochemistry
Online ISSN : 2186-2451
Print ISSN : 1344-3542
ISSN-L : 1344-3542

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UNCORRECTED PROOF
Rational Construction of Heterojunction of Bi4V2O11/Au/ZnRh2O4 to Promote Photocatalytic Overall Water Splitting
Toshihiro TAKASHIMA Tomoka SUGIHARAMasaomi YODAHikaru INOUEHiroshi IRIE
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JOURNAL OPEN ACCESS Advance online publication
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Article ID: 25-72071

UNCORRECTED PROOF: June 03, 2025
ACCEPTED MANUSCRIPT: May 21, 2025
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Abstract

The rational design of heterojunction Z-scheme photocatalysts with controlled particle alignment is critical for improving the efficiency of overall water splitting. In this study, we report the fabrication of a Z-scheme photocatalyst composed of Bi4V2O11 (BVO), Au nanoparticles and ZnRh2O4 (ZRO), with a focus on spatially aligning the constituent particles via an electrostatic assembly method. The surface of BVO was functionalized with 3-aminopropyltrimethoxysilane (APTMS) to promote the uniform deposition of Au nanoparticles, which subsequently enabled the anchoring of ZRO particles, forming a well-aligned heterojunction photocatalyst (BapAcZ). Structural and spectroscopic analyses confirmed the successful formation of the ternary composite with embedded Au between BVO and ZRO. Photocatalytic tests under monochromatic light at 700 nm revealed that BapAcZ exhibits significantly higher activity and reproducibility than randomly assembled composites, achieving an apparent quantum efficiency (AQE) of 4.7 × 10−2 %, which is 1.8 times that of the control sample. These findings highlight the importance of particle-level structural engineering in designing efficient Z-scheme systems for solar water splitting and provide insights for further development of multi-component photocatalytic systems with precisely controlled architectures.

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© The Author(s) 2025. Published by ECSJ.

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License (CC BY-NC-SA, https://creativecommons.org/licenses/by-nc-sa/4.0/), which permits non-commercial reuse, distribution, and reproduction in any medium by share-alike, provided the original work is properly cited. For permission for commercial reuse, please email to the corresponding author. [DOI: 10.5796/electrochemistry.25-72071].
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