期刊
COMPOSITES COMMUNICATIONS
卷 36, 期 -, 页码 -出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.coco.2022.101390
关键词
Hydrogen peroxide; Artificial photocatalysis; Covalent triazine framework; CsPbBr3 quantum dots; Charge separation
资金
- National Natural Science Foundation of China
- Zhejiang Provincial Natural Science Foundation of China
- 111 Project
- Foundation of Hubei Three Gorges Laboratory
- [51872147]
- [22006131]
- [LQ20B070010]
- [D20015]
- [SC213008]
This study presents a novel approach for photocatalytic hydrogen peroxide production using porous CsPbBr3 quantum dots-decorated CTFs nanocomposites. The nanocomposites exhibit significantly enhanced photocatalytic activity and achieve high solar-to-chemical conversion efficiency. This work opens up new avenues for utilizing halide perovskite quantum dots and CTFs in various photocatalytic reactions.
Hydrogen peroxide (H2O2) artificial photocatalysis technology promises a bright prospect in solving the bur-geoning energy and environmental challenges. Covalent triazine frameworks (CTFs) is an exciting group of promising photocatalysts for H2O2 production. However, single CTF still suffers from unsatisfactory photo -catalytic behavior primarily owing to the severe charge recombination and the lack of proficient dioxygen (O2) adsorption/activation catalytic sites. Herein, porous CsPbBr3 quantum dots (QDs)-decorated CTFs (CsPbBr3/ CTFs) nanocomposites were prepared through an in-situ composite method for robust photocatalytic H2O2 evolution from O2 without using any sacrificial agents. The nanocomposites exhibit a significantly boosted performance toward photocatalytic H2O2 production compared with pristine CsPbBr3 and CTFs. The reaction activity can reach a highest value of 134.6 mu M h-1, which is 13.3-times than that of the pristine CTFs. Addi-tionally, the rationally designed porous CsPbBr3/CTFs nanocomposites achieved a solar-to-chemical conversion efficiency of 0.14%, beyond most photocatalysts previously reported. The unique composite effect is key to synergistically enhance charge separation and achieve efficient H2O2 production. This work is anticipated to offer alternative avenues to exploit halide perovskite QDs and CTFs in various photocatalytic reactions.
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