摘要
Hydrogen peroxide (H 2 O 2 ) serves as a critical industrial chemical and potential energy carrier. Photocatalytic synthesis presents a viable alternative to the anthraquinone process, yet existing catalyst systems exhibit restricted sunlight wavelength responses and inadequate activity. In this study, zinc phthalocyanine/polymer carbon nitride (ZnPc/PCN) S-scheme heterojunction formation extends the photocatalyst's light absorption range to the near-infrared region (400–800 nm) and generates an internal electric field at the interface, facilitating photogenerated carrier separation and transfer. ZnPc/PCN exhibits an AQY of 1.11 % for H 2 O 2 production under 800 nm irradiation. The optimized ZnPc/PCN yields 1.87 mM H 2 O 2 , surpassing the original PCN and ZnPc by 1.36 and 93.5 times, respectively·H 2 O 2 production remains above 1.5 mM (80 %) after five cycles, demonstrating ZnPc/PCN stability. Detection of intermediate ·OOH suggests H 2 O 2 production via 2 e - oxygen reduction processes. This research offers novel insights for designing near-infrared absorbing photocatalysts.
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