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Synergistically Enhanced Photocatalytic Degradation by Coupling Slow-Photon Effect with Z-Scheme Charge Transfer in CdS QDs/IO-TiO2 Heterojunction

Molecules 2023 5 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 35 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Li‐Bang Zhu, Ning Bao, Qing Zhang, Shou‐Nian Ding

Summary

Researchers fabricated a CdS quantum dot/inverse opal TiO2 heterojunction photocatalyst that couples the slow-photon effect from the periodic inverse opal structure with Z-scheme charge transfer to simultaneously improve light absorption and reduce carrier recombination. The novel architecture achieved synergistically enhanced photocatalytic degradation performance compared to either component alone.

Polymers

Lower light absorption and faster carrier recombination are significant challenges in photocatalysis. This study introduces a novel approach to address these challenges by anchoring cadmium sulfide quantum dots (CdS QDs) on inverse opal (IO)-TiO2, which increases light absorption and promotes carriers' separation by coupling slow-photon effect with Z-scheme charge transfer. Specifically, the IO-TiO2 was created by etching a polystyrene opal template, which resulted in a periodic structure that enhances light absorption by reflecting light in the stop band. The size of CdS quantum dots (QDs) was regulated to achieve appropriate alignment of energy bands between CdS QDs and IO-TiO2, promoting carrier transfer through alterations in charge transfer modes and resulting in synergistic-amplified photocatalysis. Theoretical simulations and electrochemical investigations demonstrated the coexistence of slow-photon effects and Z-scheme transfer. The system's photodegradation performance was tested using rhodamine B as a model. This novel hierarchical structure of the Z-scheme heterojunction exhibits degradability 7.82 and 4.34 times greater than pristine CdS QDs and IO-TiO2, respectively. This study serves as a source of inspiration for enhancing the photocatalytic capabilities of IO-TiO2 and broadening its scope of potential applications.

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