Electron spin-controlled charge transfer and the resulting long-lived charge transfer state: from transition metal complexes to organic compounds

被引:15
作者
Zhang, Xue [1 ]
Chen, Xi [1 ]
Zhao, Jianzhang [1 ,2 ]
机构
[1] Dalian Univ Technol, Sch Chem Engn, State Key Lab Fine Chem, E-208 West Campus,2 Ling Gong Rd, Dalian 116021, Peoples R China
[2] Xinjiang Univ, Sch Chem, Urumqi 830046, Xinjiang, Peoples R China
关键词
TRIPLET-STATE; SEPARATED STATE; SINGLET OXYGEN; BODIPY; RECOMBINATION; DYAD; ENERGY; DESIGN; TRIAD; ION;
D O I
10.1039/d0dt03737k
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The generation of long-lived charge transfer (CT) states in electron donor/acceptor dyads upon photoexcitation is crucial for artificial photosynthesis, photocatalysis and photovoltaics. Electron spin control is a novel strategy to prolong the CT state lifetime via generation of the (CT)-C-3 triplet state, instead of the traditional short-lived (CT)-C-1 state. This method involves a local triplet excited state ((LE)-L-3) as the precursor of charge separation (CS), and the electron forbidden feature of the charge recombination (CR) of (CT)-C-3 -> S-0 vs. the electron spin allowed (CT)-C-1 -> S-0 prolongs the CT state lifetime. In this article, we summarized the recent developments and challenges in this emerging fascinating area.
引用
收藏
页码:59 / 67
页数:9
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