Traditional methods struggle to optimize active interfaces; F engineering enhances water splitting efficiency in novel photonic systems.
The highly efficient performance of photoelectrochemical (PEC) water splitting is largely governed by the construction of active interfaces, especially for the star semiconductor/electrocatalyst system. However, traditional strategies struggle to optimize this critical process. To overcome this challenge, we report a fluorine (F) engineering strategy that enables the synchronous modulation of charge transfer and surface catalytic reaction dynamics in a BiVO4/FeCoOOH-integrated photoanode. Various characterization methods confirm that F engineering can activate the BiVO4/FeCoOOH/electrolyte interfaces. Benefiting from these positive effects, the optimized BiVO4/FeCoOOH-F photoanode achieves a relatively high photocurrent density of 5.46 mA/cm2 at 1.23 V vs. RHE, along with outstanding photostability and a small Tafel slope of 96.5 mV dec−1. This study provides new insights into F-based interface manipulation, offering a promising route to developing high-performance semiconductor/electrocatalyst systems for efficient and stable PEC water splitting applications.
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Quan et al. (2026) studied this question.
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