Kim Yunseul, Kim Yeon-Ju, Kim Yeong-A, Jung Eunhwan, Mok Yoonjung, Kim Kihyeun, Hwang Hansu, Park Jong-Jin, Kim Min-Gon, Mathur Sanjay, Kim Dong-Yu
School of Materials Science and Engineering (SMSE), Research Institute for Solar and Sustainable Energies (RISE), Gwangju Institute of Science and Technology (GIST), Gwangju 61005, Republic of Korea.
Basic Materials and Chemicals R&D, LG Chem, Jeonnam 59611, Republic of Korea.
ACS Appl Mater Interfaces. 2021 Jan 20;13(2):2887-2898. doi: 10.1021/acsami.0c15893. Epub 2021 Jan 6.
While quinoidal moieties are considered as emerging platforms showing efficient charge transport and interesting open-shell diradical characteristics, whether these properties could be changed by extension to the conjugated polymer structure remains as a fundamental question. Here, we developed and characterized two conjugated polymers incorporating quinoids with different lengths, which have a stable close- and open-shell diradical character, respectively, namely, poly(quinoidal thiophene-thienylene vinylene) (PQuT-TV) and poly(quinoidal bithiophene-thienylene vinylene) (PQuBT-TV). A longer length of a quinoidal core led to enhanced diradical characteristics. Therefore, the longer core length of QuBT was favorable for the formation of an open-shell diradical structure in its monomer and in the quinoidal polymer. PQuBT-TV exhibited high spin characteristics observed by the strong ESR signal, a low band gap, and improved electrochemical stability. On the other hand, as QuT maintained a closed-shell quinoid structure, PQuT-TV exhibited high backbone coplanarity and strong intermolecular interaction, which was beneficial for charge transport and led to high hole mobility (up to 2.40 cm V s) in organic field-effect transistors. This work successfully demonstrated how the control of the closed/open-shell character of quinoidal building blocks changes charge transport and spin properties of quinoidal conjugated polymers quinoid-aromatic interconversion.
虽然醌型部分被认为是具有高效电荷传输和有趣的开壳双自由基特性的新兴平台,但这些特性是否会因扩展到共轭聚合物结构而改变仍是一个基本问题。在此,我们开发并表征了两种包含不同长度醌类的共轭聚合物,它们分别具有稳定的闭壳和开壳双自由基特性,即聚(醌型噻吩 - 亚乙烯基)(PQuT - TV)和聚(醌型联噻吩 - 亚乙烯基)(PQuBT - TV)。醌型核心长度的增加导致双自由基特性增强。因此,更长的QuBT核心长度有利于在其单体和醌型聚合物中形成开壳双自由基结构。PQuBT - TV通过强ESR信号、低带隙和改善的电化学稳定性表现出高自旋特性。另一方面,由于QuT保持闭壳醌型结构,PQuT - TV表现出高主链共面性和强分子间相互作用,这有利于电荷传输,并在有机场效应晶体管中导致高空穴迁移率(高达2.40 cm² V⁻¹ s⁻¹)。这项工作成功地证明了如何通过控制醌型结构单元的闭壳/开壳特性来改变醌型共轭聚合物的电荷传输和自旋性质——醌型 - 芳香族相互转化。