Issue 2, 2025, Issue in Progress

Tuning surface hydrophilicity of a BiVO4 photoanode through interface engineering for efficient PEC water splitting

Abstract

This study presents a novel approach to enhance photoelectrochemical (PEC) water oxidation by integrating cobalt phthalocyanine (CoPc) with bismuth vanadate (BVO) via a direct solvothermal method. The as-prepared BVO@CoPc photoanode demonstrated a photocurrent density of 4.0 mA cm−2 at 1.23 V vs. RHE, which is approximately 3.1 times greater than that of the unmodified BVO, and has superior stability. The incident photon-to-current conversion efficiency (IPCE) of the BVO@CoPc photoanode reaches an impressive value of 81%, accompanied by significant enhancements in charge injection efficiency. This excellent performance can be ascribed to the enhanced hydrophilicity with the BVO/CoPc interface engineering, which facilitates interfacial interaction between the electrode and electrolyte, accelerates photogenerated charge carrier transfer and separation. Furthermore, compared to the immersion and drop-casting methods, the BVO@CoPc-S composite photoanode prepared via the solvothermal method exhibits a significant improvement in interfacial contact and surface hydrophilicity. These findings highlight the potential of the strategy based on interfacial hydrophilicity modification to overcome key limitations in PEC water splitting, providing a pathway to more efficient and durable photoanode design.

Graphical abstract: Tuning surface hydrophilicity of a BiVO4 photoanode through interface engineering for efficient PEC water splitting

Supplementary files

Article information

Article type
Paper
Submitted
21 Nov 2024
Accepted
06 Jan 2025
First published
10 Jan 2025
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2025,15, 815-823

Tuning surface hydrophilicity of a BiVO4 photoanode through interface engineering for efficient PEC water splitting

S. Yu, C. Su, Z. Xiao, Y. Kuang, X. Gong, X. He, J. Liu, Q. Jin and Z. Sun, RSC Adv., 2025, 15, 815 DOI: 10.1039/D4RA08254K

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