非极性固态环境下j聚集的苝酰亚胺多聚体薄膜的超快对称破缺电荷分离

IF 4.2 2区化学 Q2 CHEMISTRY, MULTIDISCIPLINARY

Chemical Communications Pub Date : 2025-10-09 Epub Date: 2025-09-29 DOI:10.1039/d5cc04382d

Aniruddha Mazumder , Kavya Vinod , Amalnadh T. , Philip Daniel Maret , Ariharasudhan R. , Mahesh Hariharan

引用次数: 0

摘要

我们证明了在非极性聚甲基丙烯酸甲酯聚合物基体（ε = 2.80-3.20）中，j聚集的苝酰亚胺（PDI）多聚体薄膜的超快速对称破断电荷分离（τCS <110 fs）。理论计算揭示了通过空间电子通信和π-π相互作用促进固态PDI多晶体中超快电荷分离的作用。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

Ultrafast symmetry-breaking charge separation in thin films of J-aggregated perylenediimide multimers in a nonpolar solid-state environment

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Ultrafast symmetry-breaking charge separation in thin films of J-aggregated perylenediimide multimers in a nonpolar solid-state environment

We demonstrate ultrafast symmetry-breaking charge separation (τ_CS <110 fs) in thin films of J-aggregated perylenediimide (PDI) multimers in a nonpolar polymethyl methacrylate polymer matrix (ε = 2.80–3.20). Theoretical calculations reveal the role of through-space electronic communication and π–π interactions promoting ultrafast charge separation in PDI multimers in the solid-state.

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来源期刊

Chemical Communications 化学-化学综合

CiteScore

8.60

自引率

4.10%

发文量

2705

审稿时长

1.4 months

期刊介绍： ChemComm (Chemical Communications) is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world''s major areas of chemical research.