聚(苯并咪唑基苯并菲罗啉)(BBL)薄膜电化学转换的微观观察:分子动力学研究

IF 5.1 1区 化学 Q1 POLYMER SCIENCE Macromolecules Pub Date : 2024-06-02 DOI:10.1021/acs.macromol.4c00446
Sonu Sunny, Shivam Shah, Mohit Garg, Igor Zozoulenko* and Sarbani Ghosh*, 
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引用次数: 0

摘要

梯形苯并咪唑-苯并菲罗啉(BBL)聚合物是最重要、研究最多的 n 型导电聚合物之一。它也是一种有机混合离子电子导体(OMIEC),可以在电解质溶液中通过容纳相反离子实现电化学转换。OMIEC 材料在工作过程中发生的广泛形态变化会影响其传输特性,进而影响器件性能。然而,对电化学转换过程中动态结构变化的分子研究十分有限,因为在实验中很难或根本无法获得这些信息。基于分子动力学(MD)计算的计算显微镜可以让我们全面了解 BBL 聚合物目前在很大程度上缺失的详细动态形态变化。在本研究中,我们利用原子论 MD 模拟,从微观角度了解了 BBL 薄膜在两种不同电解质(即水中的单原子反离子 K+(钾)和氯仿中的分子反离子 DMBI+(二甲基-3-丁基咪唑))中的电化学转换。在这两种情况下,最大结晶度都可达到中等还原水平。超过这一水平后,离子插层会引发结构相变,导致薄膜的结晶阶次降低。在较高的还原水平下,单原子 K+ 反离子稳定在片状堆积的 BBL 链中;相反,分子量较高的 DMBI+ 反离子稳定在 BBL π-π 堆积中,在 BBL 和 DMBI+ 之间形成 π-π 堆积。我们的研究结果证实了分子掺杂剂如何能提高材料的热力学稳定性,以及为什么较小的单原子反离子更有利于保持较好的结晶度。BBL 薄膜在电化学转换过程中的形态变化无法通过实验直接获得,而我们从微观角度详细了解了这些变化,这无疑有助于设计基于 BBL 的 n 型 OMIEC 器件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Microscopic Insights of Electrochemical Switching of Poly(benzimidazobenzophenanthroline) (BBL) Thin Film: A Molecular Dynamics Study

The ladder-type benzimidazobenzophenanthroline (BBL) polymer is one of the most important and most studied n-type conducting polymers. It is also an organic mixed ion-electron conductor (OMIEC), which can undergo electrochemical switching in electrolyte solutions by accommodating opposite ions. The extensive morphological changes of the OMIEC material during operation affect the transport properties and, hence, the device performance. However, molecular insights into the dynamic structural changes during the electrochemical switching are limited, as they are difficult or impossible to access in experiments. The computational microscope based on molecular dynamics (MD) calculations can provide us with complete insights into the detailed dynamic morphological changes that are currently missing, to a large extent, for the BBL polymer. In the present study, using atomistic MD simulations, we obtained microscopic insights into the electrochemical switching of BBL film in two different electrolytes, namely, single-atom counterion K+ (potassium) in water and molecular counterion DMBI+ (dimethyl-3-butyl imidazolium) in chloroform. For both cases, the maximum crystallinity is found up to a moderate reduction level. Beyond that, ion intercalation initiates a structural phase transition and causes a decrease in the crystalline order of the film. At the higher reduction levels, the single-atom K+ counterions are stabilized within the lamellar stacked BBL chains; in contrast, the DMBI+ counterions with higher molecular weights are stabilized within the BBL π–π stacks, forming π–π stacking between BBL and DMBI+. Our findings substantiate how molecular dopants can improve the thermomechanical stability of the material and why smaller single-atom counterions are preferred for maintaining better crystallinity. The detailed microscopic insights into the morphological changes during the electrochemical switching of BBL film, which cannot be directly accessed experimentally, can definitely help design n-type OMIEC-based devices made of BBL.

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来源期刊
Macromolecules
Macromolecules 工程技术-高分子科学
CiteScore
9.30
自引率
16.40%
发文量
942
审稿时长
2 months
期刊介绍: Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.
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