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Encapsulating Perovskite Quantum Dots in Iron‐Based Metal–Organic Frameworks (MOFs) for Efficient Photocatalytic CO<sub>2</sub> Reduction

Liyuan WuInstitute for New Energy Materials and Low Carbon Technologies School of Chemistry and Chemical Engineering Tianjin University of Technology Tianjin 300384 ChinaYanfei MuInstitute for New Energy Materials and Low Carbon Technologies School of Chemistry and Chemical Engineering Tianjin University of Technology Tianjin 300384 ChinaXiao‐Xuan GuoInstitute for New Energy Materials and Low Carbon Technologies School of Chemistry and Chemical Engineering Tianjin University of Technology Tianjin 300384 ChinaWen ZhangInstitute for New Energy Materials and Low Carbon Technologies School of Chemistry and Chemical Engineering Tianjin University of Technology Tianjin 300384 ChinaZhiming ZhangInstitute for New Energy Materials and Low Carbon Technologies School of Chemistry and Chemical Engineering Tianjin University of Technology Tianjin 300384 ChinaMin ZhangInstitute for New Energy Materials and Low Carbon Technologies School of Chemistry and Chemical Engineering Tianjin University of Technology Tianjin 300384 ChinaTong‐Bu LuInstitute for New Energy Materials and Low Carbon Technologies School of Chemistry and Chemical Engineering Tianjin University of Technology Tianjin 300384 China
2019en
ABI

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Abstract Improving the stability of lead halide perovskite quantum dots (QDs) in a system containing water is the key for their practical application in artificial photosynthesis. Herein, we encapsulate low‐cost CH 3 NH 3 PbI 3 (MAPbI 3 ) perovskite QDs in the pores of earth‐abundant Fe‐porphyrin based metal organic framework (MOF) PCN‐221(Fe x ) by a sequential deposition route, to construct a series of composite photocatalysts of MAPbI 3 @PCN‐221(Fe x ) ( x =0–1). Protected by the MOF the composite photocatalysts exhibit much improved stability in reaction systems containing water. The close contact of QDs to the Fe catalytic site in the MOF, allows the photogenerated electrons in the QDs to transfer rapidly the Fe catalytic sites to enhance the photocatalytic activity for CO 2 reduction. Using water as an electron source, MAPbI 3 @PCN‐221(Fe 0.2 ) exhibits a record‐high total yield of 1559 μmol g −1 for photocatalytic CO 2 reduction to CO (34 %) and CH 4 (66 %), 38 times higher than that of PCN‐221(Fe 0.2 ) in the absence of perovskite QDs.

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