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Electropolymerization of Polydopamine at Electrode-Supported Insulating Mesoporous Films

介孔材料 纳米孔 材料科学 介孔二氧化硅 纳米技术 纳米孔 化学工程 介孔有机硅 电极 离子键合 表面改性 循环伏安法 薄膜 聚合物 电化学 离子 催化作用 化学 有机化学 复合材料 物理化学 工程类
作者
H. Samet Varol,Tilmann Herberger,Marius Kirsch,Joanna J. Mikolei,Lothar Veith,Venkataprasanna Kannan-Sampathkumar,Raoul D. Brand,Christopher V. Synatschke,Tanja Weil,Annette Andrieu‐Brunsen
出处
期刊:Chemistry of Materials [American Chemical Society]
卷期号:35 (21): 9192-9207 被引量:8
标识
DOI:10.1021/acs.chemmater.3c01890
摘要

Bioinspired, stimuli-responsive, polymer-functionalized mesoporous films are promising platforms for precisely regulating nanopore transport toward applications in water management, iontronics, catalysis, sensing, drug delivery, or energy conversion. Nanopore technologies still require new, facile, and effective nanopore functionalization with multi- and stimuli-responsive polymers to reach these complicated application targets. In recent years, zwitterionic and multifunctional polydopamine (PDA) films deposited on planar surfaces by electropolymerization have helped surfaces respond to various external stimuli such as light, temperature, moisture, and pH. However, PDA has not been used to functionalize nanoporous films, where the PDA-coating could locally regulate the ionic nanopore transport. This study investigates the electropolymerization of homogeneous thin PDA films to functionalize nanopores of mesoporous silica films. We investigate the effect of different mesoporous film structures and the number of electropolymerization cycles on the presence of PDA at mesopores and mesoporous film surfaces. Our spectroscopic, microscopic, and electrochemical analysis reveals that the amount and location (pores and surface) of deposited PDA at mesoporous films is related to the combination of the number of electropolymerization cycles and the mesoporous film thickness and pore size. In view of the application of the proposed PDA-functionalized mesoporous films in areas requiring ion transport control, we studied the ion nanopore transport of the films by cyclic voltammetry. We realized that the amount of PDA in the nanopores helps to limit the overall ionic transport, while the pH-dependent transport mechanism of pristine silica films remains unchanged. It was found that (i) the pH-dependent deprotonation of PDA and silica walls and (ii) the insulation of the indium-tin oxide (ITO) surface by increasing the amount of PDA within the mesoporous silica film affect the ionic nanopore transport.
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