Insights into the Enhanced Photoelectrochemical Performance through Construction of the Z-Scheme and Type II Heterojunctions

光电流 异质结 化学 分解水 光电子学 电极 载流子 半导体 光电化学 光催化 电化学 材料科学 催化作用 物理化学 生物化学
作者
Ze Wang,Xingming Ning,Yanjun Feng,Rongfang Zhang,Yaorong He,Huihuan Zhao,Jing Chen,Peiyao Du,Xiaoquan Lu
出处
期刊:Analytical Chemistry [American Chemical Society]
卷期号:94 (23): 8539-8546 被引量:18
标识
DOI:10.1021/acs.analchem.2c01607
摘要

Photoelectrochemical (PEC) water splitting technology is a promising strategy toward producing sustainable hydrogen fuel. However, it is an essential bottleneck to reduce severe charge recombination for the improvement of PEC performance. Construction of heterojunction systems, such as Z-scheme and type II heterojunctions, could efficiently boost charge separation, whereas the mechanism of charge separation is still ambiguous. We describe herein a charge transfer system designed with Bi2WO6/Bi2S3 (BWO/BS) as a prototype. In this system, Au nanoparticles act as charge relays to engineer a charge transfer pathway, and the obtained BWO/Au/BS photoanode achieves a remarkable photocurrent density of 0.094 mA cm-2 at 1.23 V versus reversible hydrogen electrode (vs RHE), over approximately 1.2 and 2.3 times larger than those of BWO/BS/Au and BWO, exhibiting long-term photostability. More importantly, scanning photoelectrochemical microscopy (SPECM) and intensity-modulated photocurrent spectroscopy (IMPS) studies are performed to in situ-capture the photogenerated hole during the PEC process. Operando analysis reveals that the Z-scheme BWO/Au/BS system (1.33 × 10-2 cm s-1) exhibits higher charge transfer kinetics compared to the type II BWO/BS/Au heterostructure (0.85 × 10-2 cm s-1) while efficiently suppressing charge recombination for optimized PEC activity. Note that this smart strategy can also be extended to other semiconductor-based photoanodes such as BiVO4. Our study offers an effective pathway for the rational design of highly efficient charge separation for solar conversion based on water splitting.
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