Ultrafast Spectroscopic Signature of Charge Transfer between Single-Walled Carbon Nanotubes and C60

被引:62
作者
Dowgiallo, Anne-Marie [1 ]
Mistry, Kevin S. [1 ,2 ]
Johnson, Justin C. [1 ]
Blackburn, Jeffrey L. [1 ]
机构
[1] Natl Renewable Energy Lab, Golden, CO 80401 USA
[2] Univ Colorado, Dept Phys, Boulder, CO 80309 USA
关键词
single-walled carbon nanotubes; fullerene; electron transfer; photovoltaic; charge generation; exciton dissociation; recombination; trion; PHOTOINDUCED ELECTRON-TRANSFER; DYNAMICS; EXCITONS; TRIONS; PHOTOVOLTAICS; COMPLEXES; FILMS;
D O I
10.1021/nn503271k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The time scales for interfacial charge separation and recombination play crucial roles in determining efficiencies of excitonic photovoltaics. Near-infrared photons are harvested efficiently by semiconducting single-walled carbon nanotubes (SWCNTs) paired with appropriate electron acceptors, such as fullerenes (e.g., C-60). However, little is known about crucial photochemical events that occur on femtosecond to nanosecond time scales at such heterojunctions. Here, we present transient absorbance measurements that utilize a distinct spectroscopic signature of charges within SWCNTs, the absorbance of a trion quasiparticle, to measure both the ultrafast photoinduced electron transfer time (tau(pet)) and yield (phi(pet)) in photoexcited SWCNT-C-60 bilayer films. The rise time of the trion-induced absorbance enables the determination of the photoinduced electron transfer (PET) time of tau(pet) <= 120 fs, while an experimentally determined trion absorbance cross section reveals the yield of charge transfer (phi(pet) approximate to 38 +/- 3%). The extremely fast electron transfer times observed here are on par with some of the best donor: acceptor pairs in excitonic photovoltaics and underscore the potential for efficient energy harvesting in SWCNT-based devices.
引用
收藏
页码:8573 / 8581
页数:9
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