Cavendish Laboratory, Department of Physics, University of Cambridge, CB3 0HE, United Kingdom.
Phys Rev Lett. 2010 Apr 30;104(17):177701. doi: 10.1103/PhysRevLett.104.177701. Epub 2010 Apr 29.
We present direct spectroscopic evidence for substantial subnanosecond charge recombination in polymer-polymer blend photovoltaic devices. Early dynamics are dominated by exciton-charge interactions associated with high initial excitation densities. Independent of density, 30% of charges subsequently recombine geminately within just 2 nanoseconds, in contrast with fullerene blends. The remainder recombines with a half-life of approximately 200 ns. The morphological invariance of subnanosecond recombination suggests that its origin is inherent in the molecular structure at the polymer-polymer interface.
我们提供了聚合物-聚合物混合光伏器件中大量亚纳秒电荷复合的直接光谱证据。早期动力学主要由与初始高激发密度相关的激子-电荷相互作用主导。与富勒烯混合物不同,独立于密度,30%的电荷随后在短短 2 纳秒内以孪生形式复合,其余电荷的复合半衰期约为 200 纳秒。亚纳秒复合的形态不变性表明,其起源是聚合物-聚合物界面处分子结构固有的。