The Role of Driving Energy and Delocalized States for Charge Separation in Organic Semiconductors

被引:1019
作者
Bakulin, Artem A. [1 ]
Rao, Akshay [1 ]
Pavelyev, Vlad G. [2 ]
van Loosdrecht, Paul H. M. [2 ]
Pshenichnikov, Maxim S. [2 ]
Niedzialek, Dorota [3 ]
Cornil, Jerome [3 ]
Beljonne, David [3 ]
Friend, Richard H. [1 ]
机构
[1] Univ Cambridge, Cavendish Lab, Cambridge CB3 0HE, England
[2] Univ Groningen, Zernike Inst Adv Mat, NL-9747 AG Groningen, Netherlands
[3] Univ Mons, Lab Chem Novel Mat, B-7000 Mons, Belgium
基金
英国工程与自然科学研究理事会;
关键词
FULLERENE SOLAR-CELLS; EXCITON DISSOCIATION; CONJUGATED POLYMER; PHOTOVOLTAIC CELLS; BINDING-ENERGY; ACCEPTOR; BLENDS; HETEROJUNCTIONS; EFFICIENT; PHOTOGENERATION;
D O I
10.1126/science.1217745
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
The electron-hole pair created via photon absorption in organic photoconversion systems must overcome the Coulomb attraction to achieve long-range charge separation. We show that this process is facilitated through the formation of excited, delocalized band states. In our experiments on organic photovoltaic cells, these states were accessed for a short time (<1 picosecond) via infrared (IR) optical excitation of electron-hole pairs bound at the heterojunction. Atomistic modeling showed that the IR photons promote bound charge pairs to delocalized band states, similar to those formed just after singlet exciton dissociation, which indicates that such states act as the gateway for charge separation. Our results suggest that charge separation in efficient organic photoconversion systems occurs through hot-state charge delocalization rather than energy-gradient-driven intermolecular hopping.
引用
收藏
页码:1340 / 1344
页数:5
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