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首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Primary Dynamics of Exciton and Charge Photogeneration in Solvent Vapor Annealed P3HT/PCBM Films
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Primary Dynamics of Exciton and Charge Photogeneration in Solvent Vapor Annealed P3HT/PCBM Films

机译:溶剂蒸气退火的P3HT / PCBM膜中激子和电荷光生的主要动力学

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摘要

The primary dynamics of exciton and charge photogeneration in the neat P3HT (poly(3-hexylthiophene)) and the blend P3HT/PCBM ([6,6]-phenyl-C61-butyric acid methyl ester) films were investigated by the use of near-infrared femtosecond transient absorption spectroscopy with varying excitation photon energy and fluence. The effects of film morphology were examined by comparing the solvent vapor annealed (SVA) and the carbon disulfide (CS2) cast films. Spectroelectrochemistry was employed to characterize the cationic polaron P3HT~(·+) to facilitate the assignments of the transient spectra. Time-resolved spectroscopy revealed two different types of polarons, the delocalized (DP, absorbing over 630-830 nm) and the localized (LP, 750-1100 nm) ones inhabiting the crystalline and the disordered P3HT phases, respectively. In addition, the characteristic absorption of the long-sought anionic polaron P3HT~(·+) is proposed to be a broad-band spectrum extending up to ~1300 nm with a maximum at ~1080 nm. For SVA neat P3HT films under the low-fluence photoexcitation, ~10~(12) photons·cm~(-2) pulse~(-1), the overall polaron yield (DP + LP) at 1.45 ns was determined to be <7% after the blue-edge excitation at 460 nm, or to be negligible after the red-edge excitation at 620 nm. For the P3HT/PCBM blends under the low-fluence photoexcitation, the prompt and the delayed polaron formation with comparable contribution are found to be independent of the excitation wavelengths; the former is governed by the instantaneous charge separation at the donor-acceptor interfaces, whereas the latter relies on the exciton diffusion in P3HT crystallites with a time constant of 7-10 ps. The effects of film morphology and photon energy on the charge photogeneration dynamics are discussed in terms of the disordered intermediate between the P3HT crystallite and the PCBM aggregate, which is suggested to be in less dimension for SVA films than that for thermally annealed films, and thereby to be advantageous in minimizing the traps or blocks of charge carriers.
机译:通过使用近红外光谱研究了纯P3HT(聚(3-己基噻吩))和P3HT / PCBM共混物([6,6]-苯基-C61-丁酸甲酯)薄膜中激子和电荷光生化的主要动力学。激发光子能量和能量密度变化的红外飞秒瞬态吸收光谱。通过比较溶剂蒸汽退火(SVA)和二硫化碳(CS2)流延膜来检验膜形态的影响。光谱电化学用于表征阳离子极化子P3HT〜(·+),以利于瞬态光谱的分配。时间分辨光谱法显示了两种不同类型的极化子,分别位于晶体和无序P3HT相的离域(DP,吸收630-830 nm)和局域(LP,750-1100 nm)。此外,长期以来寻求的阴离子极化子P3HT〜(·+)的特征吸收被认为是一个宽带光谱,扩展到〜1300 nm,最大在〜1080 nm。对于低通量光激发〜10〜(12)光子·cm〜(-2)脉冲〜(-1)的SVA纯P3HT薄膜,在1.45 ns处的总极化子产率(DP + LP)确定为<在460 nm的蓝边激发后为7%,或者在620 nm的红边激发后可以忽略不计。对于低通量光激发下的P3HT / PCBM共混物,发现迅速和延迟的极化子形成具有可比的贡献,这与激发波长无关。前者由施主与受主界面的瞬时电荷分离控制,而后者则依赖于P3HT微晶中的激子扩散,其时间常数为7-10 ps。根据P3HT微晶与PCBM聚集体之间的无序中间物,讨论了膜形态和光子能量对电荷光生动力学的影响,这表明SVA膜的尺寸小于热退火膜的尺寸,因此在最小化电荷载流子的陷阱或块方面是有利的。

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