导电体
生物电子学
材料科学
溶剂化
聚合物
兴奋剂
电化学
化学物理
导电聚合物
离子
纳米技术
电导率
联轴节(管道)
氢
化学工程
分子
储能
超分子化学
氢气储存
电荷(物理)
电解质
电阻率和电导率
有机聚合物
载流子
作者
Tom P. A. van der Pol,Dongxun Lyu,Zoé Truyens,Vincent Lemaur,Δήμητρα Τσόκκου,Arianna Magni,Chiara Musumeci,Han-Yan Wu,Junpeng Ji,David Cornil,C.-L. Yang,Scott T. Keene,Gabriele D’Avino,Alberto Salleo,Natalie Banerji,Clare Grey,David Beljonne,Simone Fabiano
出处
期刊:Nature Materials
[Nature Portfolio]
日期:2026-02-11
卷期号:25 (5): 832-839
被引量:1
标识
DOI:10.1038/s41563-025-02478-2
摘要
Abstract Controlling ion–polymer interactions in organic mixed ionic-electronic conductors is crucial for optimizing device performance in applications ranging from bioelectronics and energy storage to photonics. Achieving this requires a molecular-level understanding of how ion uptake, solvation and polymer structure evolve during electrochemical doping. Here using a multimodal operando approach, we uncover an unexpected response in the prototypical n-type ladder polymer poly(benzimidazobenzophenanthroline) (BBL) on doping with protic cations such as ammonium. At high doping levels, strong ion–polymer interactions (primarily hydrogen bonding) between cations and the BBL backbone promote charge localization and disrupt ion hydration, leading to a pronounced reduction in mass and thickness. Operando 2 H NMR identifies water expulsion, rather than ion removal, as the origin of this deswelling. Our combined experimental and modelling results reveal a previously unobserved regime of ion–polymer coupling in organic mixed ionic-electronic conductors, establishing a framework for material design and applications that span (bio-)electronics to photonics.
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