Niklas Jens, Holt Josh M, Mistry Kevin, Rumbles Garry, Blackburn Jeffrey L, Poluektov Oleg G
†Chemical Sciences and Engineering Division, Argonne National Laboratory, 9700 South Cass Avenue, Argonne, Illinois 60439, United States.
‡Chemical and Materials Science Center, National Renewable Energy Laboratory, 15013 Denver West Pkwy, Golden, Colorado 80401, United States.
J Phys Chem Lett. 2014 Feb 6;5(3):601-6. doi: 10.1021/jz402668h. Epub 2014 Jan 28.
Single-wall carbon nanotubes (SWCNTs) could be employed in organic photovoltaic (OPV) devices as a replacement or additive for currently used fullerene derivatives, but significant research remains to explain fundamental aspects of charge generation. Electron paramagnetic resonance (EPR) spectroscopy, which is sensitive only to unpaired electrons, was applied to explore charge separation in P3HT:SWCNT blends. The EPR signal of the P3HT positive polaron increases as the concentration of SWCNT acceptors in a photoexcited P3HT:SWCNT blend is increased, demonstrating long-lived charge separation induced by electron transfer from P3HT to SWCNTs. An EPR signal from reduced SWCNTs was not identified in blends due to the free and fast-relaxing nature of unpaired SWCNT electrons as well as spectral overlap of this EPR signal with the signal from positive P3HT polarons. However, a weak EPR signal was observed in chemically reduced SWNTs, and the g values of this signal are close to those of C70-PCBM anion radical. The anisotropic line shape indicates that these unpaired electrons are not free but instead localized.
单壁碳纳米管(SWCNTs)可用于有机光伏(OPV)器件,作为当前使用的富勒烯衍生物的替代品或添加剂,但仍需大量研究来解释电荷产生的基本方面。仅对未成对电子敏感的电子顺磁共振(EPR)光谱被用于探索P3HT:SWCNT混合物中的电荷分离。在光激发的P3HT:SWCNT混合物中,随着SWCNT受体浓度的增加,P3HT正极化子的EPR信号增强,这表明从P3HT到SWCNTs的电子转移诱导了长寿命的电荷分离。由于未成对的SWCNT电子具有自由且快速弛豫的特性,以及该EPR信号与P3HT正极化子信号的光谱重叠,在混合物中未识别出还原SWCNTs的EPR信号。然而,在化学还原的SWNTs中观察到一个微弱的EPR信号,该信号的g值与C70-PCBM阴离子自由基的g值接近。各向异性的线形表明这些未成对电子不是自由的,而是局域化的。