Recent Developments on Understanding Charge Transfer in Molecular Electron Donor-Acceptor Systems

被引:58
作者
Chen, Xi [1 ]
Zhang, Xue [1 ]
Xiao, Xiao [1 ]
Wang, Zhijia [2 ]
Zhao, Jianzhang [1 ,3 ]
机构
[1] Dalian Univ Technol, Frontier Sci Ctr Smart Mat, Sch Chem Engn, State Key Lab Fine Chem, 2 Ling Gong Rd, Dalian 116024, Peoples R China
[2] Capital Normal Univ, Dept Chem, Beijing 100048, Peoples R China
[3] Xinjiang Univ, Coll Chem, State Key Lab Chem & Utilizat Carbon Based Energy, Urumqi 830017, Peoples R China
关键词
Charge Transfer; Electron Spin Transfer; Intersystem Crossing; Photochemistry; Thermally Activated Delayed Fluorescence; RADICAL-ION PAIRS; PHOTOEXCITED TRIPLET-STATE; SPIN POLARIZATION TRANSFER; TIME-RESOLVED EPR; SYMMETRY-BREAKING; SEPARATED STATE; ENERGY-TRANSFER; FLUORESCENCE; RECOMBINATION; CHROMOPHORE;
D O I
10.1002/anie.202216010
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Charge transfer (CT) in molecular electron donor-acceptor systems is pivotal for artificial photosynthesis, photocatalysis, photovoltaics and fundamental photochemistry. We summarized the recent development in study of CT and discussed its application in thermally activated delayed fluorescence (TADF) emitters. The direct experimental proof of the spin multiplicity of the charge separated (CS) state with pulsed laser excited time-resolved electron paramagnetic resonance (TREPR) spectroscopy was discussed. Experimental determination of the electron exchange energy (J) of the CS state, with magnetic field effect on its yield or lifetime was introduced. The electron spin transfer accompanying the CT, studied with pulsed EPR spectra was briefly discussed. Tuning of the CT yield and kinetics with selective vibration excitation of the linker (the bridge) with IR pulse was presented. Above all, these studies show that there are more fun than simply monitoring the formation of the cations and anions and the kinetics or CS yields in this area.
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页数:27
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