Efficient Proton Transfer and Charge Separation within Covalent Organic Frameworks via Hydrogen-Bonding Network to Boost H 2 O 2 Photosynthesis

Photocatalytic synthesis based on the oxygen reduction reaction (ORR) has shown great promise for H O production. However, the low activity and selectivity of 2e ORR result in a fairly low efficiency of H O production. Herein, we propose a strategy to enhance the proton-coupled electron transfer (PC...

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Veröffentlicht in:Nano letters 2024-05, Vol.24 (21), p.6302-6311
Hauptverfasser: Lin, Yan, Zou, Juncong, Wu, Xin, Tong, Shehua, Niu, Qiuya, He, Shanying, Luo, Shenglian, Yang, Chunping
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Sprache:eng
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Zusammenfassung:Photocatalytic synthesis based on the oxygen reduction reaction (ORR) has shown great promise for H O production. However, the low activity and selectivity of 2e ORR result in a fairly low efficiency of H O production. Herein, we propose a strategy to enhance the proton-coupled electron transfer (PCET) process in covalent organic frameworks (COFs), thereby significantly boosting H O photosynthesis. We demonstrated that the construction of a hydrogen-bonding network, achieved by anchoring the H PO molecular network on COF nanochannels, can greatly improve both proton conductivity and photogenerated charge separation efficiency of COFs. Thus, COF@H PO exhibited superior photocatalytic performance in generating H O without sacrificial agents, with a solar-to-chemical conversion efficiency as high as 0.69%. Results indicated that a much more localized spatial distribution of energy band charge density on COF@H PO led to efficient charge separation, and the small energy barrier of the rate-limiting step from *OOH to H O endowed COF@H PO with higher 2e ORR selectivity.
ISSN:1530-6984
1530-6992
DOI:10.1021/acs.nanolett.4c01048