使用烷基膦酸改性剂改善电致变色聚合物-透明氧化物电极界面的相互作用

IF 3.1 4区 工程技术 Q2 POLYMER SCIENCE
Keith E. Johnson, D. Eric Shen, John R. Reynolds, Aubrey L Dyer
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引用次数: 0

摘要

随着制备可溶液加工电致变色聚合物的新合成方法的探索,包括合成规模不断扩大,超出研究实验室的范围,预计聚合物分子间和分子内的相互作用将受到影响。在本研究中,我们探讨了使用四种不同链长的烷基膦酸对 ITO 透明电极进行界面处理,以改善聚合物与电极之间的相互作用,从而减轻薄膜在反复氧化/还原和膨胀/溶胀过程中的完整性损失以及由此产生的电致变色特性(电流密度、光学特性和有效开关速率)。研究发现,膦酸层可以使电极表面与聚合物层的极性相容,同时还能改善表面能量的均匀性。我们评估了两种电致变色聚合物 (ECP),虽然在未经处理的 ITO 上观察到近乎完全的分层,但在涂覆到十二烷基膦酸上后,薄膜的完整性在重复 25 次循环后仍能保持,聚合物的光学对比度在所有开关速率下均能保持。此外,我们还表明,电致变色聚合物薄膜的完整性可在一定薄膜厚度范围内保持不变。这种方法可以推广到使用各种与金属氧化物表面接触的可溶液加工电活性聚合物的应用中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Improving interactions at the electrochromic polymer‐transparent oxide electrode interface using alkyl phosphonic acid modifiers
As new synthetic methods for the preparation of solution processable electrochromic polymers are explored, including increasing synthetic scale beyond that of the research laboratory, it is expected that polymer intermolecular and intramolecular interactions will be affected. In this study, we explore the use of four different alkyl phosphonic acids of differing chain lengths as an interfacial treatment on ITO transparent electrodes to improve the polymer‐electrode interactions to mitigate the loss of film integrity and resulting electrochromic properties (current density, optical properties, and effective switch rates) during repeated oxidation/reduction and swelling/deswelling of the film. It was found that the phosphonic acid layer allows for a compatibilization of the polarity of the electrode surface with the polymer layer while also improving surface energy uniformity. We evaluated two electrochromic polymers (ECPs), and while a near complete delamination was observed on untreated ITO, film integrity was maintained beyond 25 repeated cycles, with polymer optical contrast maintained at all switching rates when coated onto dodecylphosphonic acid. Additionally, we show that electrochromic polymer film integrity is maintained over a range of film thicknesses. This method can be extended to applications using a variety of solution processable electroactive polymers in contact with metal oxide surfaces.
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来源期刊
Polymers for Advanced Technologies
Polymers for Advanced Technologies 工程技术-高分子科学
CiteScore
6.20
自引率
5.90%
发文量
337
审稿时长
2.1 months
期刊介绍: Polymers for Advanced Technologies is published in response to recent significant changes in the patterns of materials research and development. Worldwide attention has been focused on the critical importance of materials in the creation of new devices and systems. It is now recognized that materials are often the limiting factor in bringing a new technical concept to fruition and that polymers are often the materials of choice in these demanding applications. A significant portion of the polymer research ongoing in the world is directly or indirectly related to the solution of complex, interdisciplinary problems whose successful resolution is necessary for achievement of broad system objectives. Polymers for Advanced Technologies is focused to the interest of scientists and engineers from academia and industry who are participating in these new areas of polymer research and development. It is the intent of this journal to impact the polymer related advanced technologies to meet the challenge of the twenty-first century. Polymers for Advanced Technologies aims at encouraging innovation, invention, imagination and creativity by providing a broad interdisciplinary platform for the presentation of new research and development concepts, theories and results which reflect the changing image and pace of modern polymer science and technology. Polymers for Advanced Technologies aims at becoming the central organ of the new multi-disciplinary polymer oriented materials science of the highest scientific standards. It will publish original research papers on finished studies; communications limited to five typewritten pages plus three illustrations, containing experimental details; review articles of up to 40 pages; letters to the editor and book reviews. Review articles will normally be published by invitation. The Editor-in-Chief welcomes suggestions for reviews.
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