摘要
The co-existence of diverse antibiotics in wastewater systems necessitates the development of multifunctional catalysts for simultaneous pollutant remediation. While indium oxide (In 2 O 3 ) presents advantages as a semiconductor photocatalyst through its high electrical conductivity, low resistivity, and inherent oxygen vacancies, practical applications in broad-spectrum pollutant degradation remain constrained by rapid charge carrier recombination and limited visible-light utilization efficiency. To address these challenges, we developed plasmonic Au nanoparticle-decorated In 2 O 3 composites (Au NPs /In 2 O 3 ) via a controlled in-situ reduction strategy. Systematic characterization revealed that the localized surface plasmon resonance (LSPR) effect of Au nanoparticles synergistically enhanced UV–vis absorption characteristics while effectively suppressing photogenerated electron-hole recombination, as evidenced by photoelectrochemical analyses including transient photocurrent response and electrochemical impedance spectroscopy. The optimized Au NPs /In 2 O 3 hybrid demonstrated exceptional photocatalytic performance, achieving 99.0 % degradation efficiency for both ofloxacin and tetracycline antibiotics under visible-light irradiation, along with remarkable cycling stability (>90 % efficiency retention after three cycles) and practical applicability across varied water matrices. Mechanistic investigations through radical trapping experiments identified the predominant roles of hole (h + ) and superoxide radical (·O 2 − ) species in the multi-pathway degradation processes. This study not only provides an effective strategy for engineering plasmon-enhanced In 2 O 3 photocatalysts but also establishes a methodological framework for developing multifunctional catalytic systems for environmental remediation.
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