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Structure–property–performance correlation in BiVO 4 photoanodes synthesized by intensity-tuned pulse electrodeposition

材料科学 钒酸铋 X射线光电子能谱 光电流 介电谱 拉曼光谱 微晶 分析化学(期刊) 析氧 扫描电子显微镜 分解水 电化学 化学工程 脉冲激光沉积 钒酸盐 光谱学 光电子学 沉积(地质) 化学浴沉积 表面电荷 光电化学电池 热氧化 基质(水族馆) 表面光电压
作者
Nguyễn Thị Minh Huyền,Thi Viet Ha Luu,Tran Le,Huu Phuc Dang
出处
期刊:Nanoscale advances [Royal Society of Chemistry]
卷期号:7 (22): 7182-7195 被引量:2
标识
DOI:10.1039/d5na00667h
摘要

The development of efficient and stable photoanodes is critical for advancing photoelectrochemical (PEC) water splitting technologies. In this work, bismuth vanadate (BiVO4) photoanodes were fabricated using a two-step method combining the pulse electrodeposition of bismuth and spin-coating of a vanadium precursor [VO(acac)2], followed by thermal annealing. By systematically varying the pulse voltages and vanadium precursor volume, a series of samples were produced. The sample labeled Bi-576 (deposited at 1.5-1.7 V with 0.6 μL VO(acac)2) exhibited the highest PEC performance. This optimized sample achieved a photocurrent density of 1.33 mA cm-2 at 1.23 V vs. RHE, with an applied bias photon-to-current efficiency (ABPE) of 20% and a charge injection efficiency of 60.1% under AM 1.5G illumination. Structural analysis via X-ray diffraction revealed a preferential (121) crystal orientation and reduced crystallite size, promoting directional charge transport and suppressing recombination. Raman and X-ray photoelectron spectroscopy confirmed the presence of Bi3+, V5+, and strong V-O bonding, along with surface oxygen species that enhance charge separation and interfacial transfer. Field-emission scanning electron microscopy showed a porous, interconnected morphology that increased the electrochemical active surface area (ECSA). Electrochemical impedance spectroscopy and Mott-Schottky analysis revealed a high donor density of 8.65 × 1020 cm-3 and a long interfacial time constant (τ int) of 31.46 ms, both contributing to efficient charge transport. Stability tests showed that Bi-576 retained over 82% of its photocurrent after 10 hours of continuous operation, indicating excellent long-term durability. These results demonstrate that tuning the pulse deposition conditions and precursor chemistry enables the rational design of BiVO4 photoanodes with optimized structural and electronic properties. This scalable approach offers a promising route for the development of high-performance photoanodes for solar-driven water splitting.

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