Photogenerated Charge Separation in a CdSe Nanocluster Encapsulated in a Metal-Organic Framework for Improved Photocatalysis

被引:21
作者
Choudhuri, Indrani [1 ,2 ]
Truhlar, Donald G. [1 ,2 ]
机构
[1] Univ Minnesota, Chem Theory Ctr, Dept Chem, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Minnesota Supercomp Inst, Minneapolis, MN 55455 USA
关键词
HYDROGEN EVOLUTION; HETEROGENEOUS PHOTOCATALYST; ENERGY-TRANSFER; BAND-GAPS; EFFICIENT; NU-1000; DESIGN; FUNCTIONALIZATION; CATALYST; SULFIDE;
D O I
10.1021/acs.jpcc.0c00007
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Nanoclusters encapsulated in a metal-organic framework (MOF) are the subject of intense interest because of their high promise for photocatalysis. We show computationally that a CdSe nanocluster incorporated into NU-1000 (Cd6Se6@NU-1000) allows electron transfer from a visible-light photo-excited organic linker to the lowest unoccupied crystal orbital of the inorganic cluster, which can lead to charge separation. Substituents on the linker can be used to tune the band position and the band gap of the whole composite (Cd6Se6@NU-1000), and this makes it possible to perform the water splitting reaction under visible light. The achievement of charge separation within the MOF leads to longer life of the excited states, and as a result, it can enhance the photocatalytic activity of the system.
引用
收藏
页码:8504 / 8513
页数:10
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