A CMP-based [FeFe]-hydrogenase dual-functional biomimetic system for photocatalytic hydrogen evolution coupled with degradation of tetracycline

A novel bio-inspired conjugated microporous polymer (CMP) had been designed, synthesized and characterized. The mimics of [FeFe]-hydrogenase active sites were covalently attached to the CMP skeleton, which facilitates charge transfer between the light-harvesting moiety and active sites, and exhibite...

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Veröffentlicht in:Applied catalysis. B, Environmental Environmental, 2024-01, Vol.340, p.123200, Article 123200
Hauptverfasser: Feng, Guangyuan, Sun, Yajing, Yuan, Jiangyan, Qian, Jingyu, Siam, Nasreldeen, Fa, Dejuan, Ji, Wenyan, Zhang, Enbing, Shen, Yongtao, Yan, Jing, Lei, Shengbin, Hu, Wenping
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Sprache:eng
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Zusammenfassung:A novel bio-inspired conjugated microporous polymer (CMP) had been designed, synthesized and characterized. The mimics of [FeFe]-hydrogenase active sites were covalently attached to the CMP skeleton, which facilitates charge transfer between the light-harvesting moiety and active sites, and exhibited high performance in visible-light photocatalytic hydrogen evolution (2120 μmol·h−1·g−1) in an aqueous solution. The flower-like morphology, covalently linked framework and the “single active-site” effect derived from the porous skeleton were deemed to go a long way toward boosting the properties above. Interestingly, when the electron sacrifice agent (triethanolamine) was replaced by tetracycline, the CMP-based photocatalyst maintained the capability of photocatalytic hydrogen production (370 μmol·h−1·g−1) and realized efficient photodegradation of tetracycline simultaneously. This work provides a heuristic green dual-function strategy for constructing a sustainable and efficient photocatalytic system for hydrogen evolution with concurrent antibiotic residue degradation. [Display omitted] •CMP-based [FeFe]-hydrogenase biomimetic system were achieved.•A sustainable and efficient dual-function photocatalytic system was constructed by covalent link [2Fe2S] site to CMP skeleton.
ISSN:0926-3373
1873-3883
DOI:10.1016/j.apcatb.2023.123200