Lead halide perovskites for photocatalytic organic synthesis

被引:296
|
作者
Zhu, Xiaolin [1 ]
Lin, Yixiong [1 ]
San Martin, Jovan [1 ]
Sun, Yue [1 ]
Zhu, Dian [1 ]
Yan, Yong [1 ]
机构
[1] San Diego State Univ, Dept Chem & Biochem, San Diego, CA 92182 USA
基金
美国国家科学基金会;
关键词
LIGHT PHOTOREDOX CATALYSIS; ANION-EXCHANGE; HIGHLY LUMINESCENT; OPTICAL-PROPERTIES; NANOCRYSTALS; ELECTRON; LIGAND; BR; CL; ALKYLATION;
D O I
10.1038/s41467-019-10634-x
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Nature is capable of storing solar energy in chemical bonds via photosynthesis through a series of C-C, C-O and C-N bond-forming reactions starting from CO2 and light. Direct capture of solar energy for organic synthesis is a promising approach. Lead (Pb)-halide perovskite solar cells reach 24.2% power conversion efficiency, rendering perovskite a unique type material for solar energy capture. We argue that photophysical properties of perovskites already proved for photovoltaics, also should be of interest in photoredox organic synthesis. Because the key aspects of these two applications are both relying on charge separation and transfer. Here we demonstrated that perovskites nanocrystals are exceptional candidates as photocatalysts for fundamental organic reactions, for example C-C, C-N and C-O bond-formations. Stability of CsPbBr3 in organic solvents and ease-of-tuning their bandedges garner perovskite a wider scope of organic substrate activations. Our low-cost, easy-to-process, highly-efficient, air-tolerant and bandedge-tunable perovskites may bring new breakthrough in organic chemistry.
引用
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页数:10
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