Ultrafast charge carrier dynamics in potassium-doped endohedral metallofullerene Sc3N@C80 thin films

被引:5
作者
Emmerich, Sebastian [1 ,3 ]
Hedwig, Sebastian [1 ]
Cinchetti, Mirko [2 ]
Stadtmueller, Benjamin [1 ]
Aeschlimann, Martin [1 ]
机构
[1] Univ Kaiserslautern, Erwin Schrodinger Str 46, D-67663 Kaiserslautern, Germany
[2] Tech Univ Dortmund, Expt Phys 6, D-44221 Dortmund, Germany
[3] Fraunhofer Inst Ind Math ITWM, Div Math Vehicle Engn MF, Fraunhofer Pl 1, D-67663 Kaiserslautern, Germany
基金
欧洲研究理事会;
关键词
Ultrafast exciton dynamics; Molecular thin films; Endohedral metallofullerene; Time- and angle-resolved photoelectron spectroscopy; Alkali metal doping; RESOLVED PHOTOEMISSION; ELECTRONIC STATES; EXCITON DYNAMICS; C-60; FULLERENES; SEPARATION; EFFICIENCY;
D O I
10.1016/j.elspec.2021.147110
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
Molecular materials have emerged as highly flexible platform for photovoltaic and light-harvesting applications. One of the most important challenges for this class of materials is the trapping of charge carriers in bound electron-hole pairs, which severely limits the free charge carrier generation. Here, we demonstrate a significant modification of the exciton dynamics in thin films of endohedral metallofullerene complexes upon alkali metal doping. For the exemplary case of Sc3N@C-80 thin films, we show that potassium doping results in an additional relaxation channel for the optically excited charge-transfer excitons that prevents the trapping of excitons in a long-lived Frenkel exciton-like state. Instead, potassium doping leads to an ultrafast exciton dissociation and most likely to the generation of free charge carriers. In this way, we propose alkali metal doping of molecular films as a novel approach to enhance the light-to-charge carrier conversion efficiency in photovoltaic molecular materials.
引用
收藏
页数:8
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