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Despite significant progress in photoelectrochemical (PEC) water splitting, high fabrication costs and limited efficiency of photoanodes hinder practical applications. Bismuth vanadate (BiVO), with its low cost, non-toxicity, and suitable band structure, is a promising photoanode material but suffers from poor charge transport, sluggish surface kinetics, and photocorrosion. In this study, porous monoclinic BiVO films are fabricated via a simplified successive ionic layer adsorption and reaction (SILAR) method, followed by borate treatment and PEC deposition of NiFeO. The resulting B/BiVO/NiFeO photoanode exhibits a significantly enhanced photocurrent density of 2.45 mA cm at 1.23 V vs. RHE-5.3 times higher than pristine BiVO. It also achieves an ABPE of 0.77% and a charge transfer efficiency of 79.5%. These results demonstrate that dual surface modification via borate and NiFeO is a cost-effective strategy to improve BiVO-based PEC water splitting performance. This work provides a promising pathway for the scalable development of efficient and economically viable photoanodes for solar hydrogen production.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12388382 | PMC |
http://dx.doi.org/10.3390/mi16080866 | DOI Listing |
Micromachines (Basel)
July 2025
Key Laboratory of Low-Dimensional Structural Physics and Application, Education Department of Guangxi Zhuang Autonomous Region, College of Physics and Electronic Information Engineering, Guilin University of Technology, Guilin 541004, China.
Despite significant progress in photoelectrochemical (PEC) water splitting, high fabrication costs and limited efficiency of photoanodes hinder practical applications. Bismuth vanadate (BiVO), with its low cost, non-toxicity, and suitable band structure, is a promising photoanode material but suffers from poor charge transport, sluggish surface kinetics, and photocorrosion. In this study, porous monoclinic BiVO films are fabricated via a simplified successive ionic layer adsorption and reaction (SILAR) method, followed by borate treatment and PEC deposition of NiFeO.
View Article and Find Full Text PDFJ Phys Chem Lett
June 2025
Department of Chemical System Engineering, School of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656, Japan.
The corrosion of anode materials caused by dissolved chloride ions (Cl) is considered one of the most significant issues in the long term durability of seawater electrolysis systems. This study examined the corrosion behaviors of Ni-based electrodes based on a dynamic potential-pH (Pourbaix) diagram with various buffered electrolytes (borate, carbonate, and phosphate). It was found that NiFeO/Ni plate electrodes degraded faster in media with mild pH than those with alkaline pH, and the corrosion rate depended on the dissolved ionic species in the presence of Cl, which could be explained in terms of the thermodynamic stability of the formed compounds on the surface.
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