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聚(3-己基噻吩)晶域中的一维单线态激子扩散

One-Dimensional Singlet Exciton Diffusion in Poly(3-hexylthiophene) Crystalline Domains.

作者信息

Tamai Yasunari, Matsuura Yuu, Ohkita Hideo, Benten Hiroaki, Ito Shinzaburo

机构信息

†Department of Polymer Chemistry, Graduate School of Engineering, Kyoto University, Katsura, Nishikyo, Kyoto 615-8510, Japan.

‡Japan Science and Technology Agency (JST), PRESTO, 4-1-8 Honcho, Kawaguchi, Saitama 332-0012, Japan.

出版信息

J Phys Chem Lett. 2014 Jan 16;5(2):399-403. doi: 10.1021/jz402299a. Epub 2014 Jan 9.

Abstract

Singlet exciton dynamics in crystalline domains of regioregular poly(3-hexylthiophene) (P3HT) films was studied by transient absorption spectroscopy. Upon the selective excitation of crystalline P3HT at the absorption edge, no red shift of the singlet exciton band was observed with an elapse of time, suggesting singlet exciton dynamics in relatively homogeneous P3HT crystalline domains without downhill relaxation in the energetic disorder. Even under such selective excitation conditions, the annihilation rate coefficient γ(t) was still dependent on time, γ(t) ∝ t(-1/2), which is attributed to anisotropic exciton diffusion in P3HT crystalline domains. From the annihilation rate coefficient, the singlet exciton diffusion coefficient D and exciton diffusion length LD in the crystalline domains were evaluated to be 7.9 × 10(-3) cm(2) s(-1) and 20 nm, respectively. The origin of the time-dependent exciton dynamics is discussed in terms of dimensionality.

摘要

通过瞬态吸收光谱研究了区域规整聚(3-己基噻吩)(P3HT)薄膜晶域中的单线态激子动力学。在吸收边缘对结晶P3HT进行选择性激发时,随着时间的推移,未观察到单线态激子带的红移,这表明在相对均匀的P3HT晶域中,单线态激子动力学不存在能量无序下的向下弛豫。即使在这种选择性激发条件下,湮灭速率系数γ(t) 仍与时间有关,γ(t) ∝ t^(-1/2),这归因于P3HT晶域中的各向异性激子扩散。根据湮灭速率系数,晶域中的单线态激子扩散系数D和激子扩散长度LD分别评估为7.9 × 10^(-3) cm^(2) s^(-1) 和20 nm。从维度的角度讨论了与时间相关的激子动力学的起源。

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