离域电子
光诱导电荷分离
皮秒
光电子学
激发态
有机半导体
分子间力
电子
材料科学
离解(化学)
化学物理
载流子
凝聚态物理
化学
原子物理学
激子
分子物理学
物理
光催化
分子
人工光合作用
物理化学
量子力学
催化作用
生物化学
有机化学
激光器
作者
Artem A. Bakulin,Akshay Rao,Vlad G. Pavelyev,P. H. M. van Loosdrecht,Maxim S. Pshenichnikov,Dorota Niedziałek,Jérôme Cornil,David Beljonne,Richard H. Friend
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2012-02-24
卷期号:335 (6074): 1340-1344
被引量:1156
标识
DOI:10.1126/science.1217745
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI