Polyaniline nanowire arrays generated through oriented mesoporous silica films: effect of pore size and spectroelectrochemical response

IF 3.1 3区 化学 Q2 CHEMISTRY, PHYSICAL
Wahid Ullah, Grégoire Herzog, Neus Vilà and Alain Walcarius
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引用次数: 3

Abstract

Indium–tin oxide electrodes modified with vertically aligned silica nanochannel membranes have been produced by electrochemically assisted self-assembly of cationic surfactants (cetyl- or octadecyl-trimethylammonium bromide) and concomitant polycondensation of the silica precursors (tetraethoxysilane). They exhibited pore diameters in the 2–3 nm range depending on the surfactant used. After surfactant removal, the bottom of mesopores was derivatized with aminophenyl groups via electrografting (i.e., electrochemical reduction of in situ generated aminophenyl monodiazonium salt). These species covalently bonded to the ITO substrate were then exploited to grow polyaniline nanofilaments by electropolymerization of aniline through the nanochannels. Under potentiostatic conditions, the length of polyaniline wires is controllable by tuning the electropolymerization time. From cyclic voltammetry characterization performed either before or after dissolution of the silica template, it appeared that both the polyaniline/silica composite and the free polyaniline nanowire arrays were electroactive, yet with much larger peak currents in the latter case as a result of larger effective surface area offered to the electrolyte solution. At identical electropolymerization time, the amount of deposited polyaniline was larger when using the silica membrane with larger pore diameter. All polyaniline deposits exhibited electrochromic properties. However, the spectroelectrochemical data indicated more complete interconversion between the coloured oxidized form and colourless reduced polyaniline for the arrays of nanofilaments in comparison to bulky films. In addition, the template-free nanowire arrays (i.e., after silica dissolution) were characterized by faster electrochromic behaviour than the polyaniline/silica hybrid, confirming the potential interest of such polyaniline nano-brushes for practical applications.

Abstract Image

定向介孔二氧化硅膜制备聚苯胺纳米线阵列:孔径和光谱电化学响应的影响
通过电化学辅助阳离子表面活性剂(十六烷基或十八烷基三甲基溴化铵)的自组装和二氧化硅前体(四乙氧基硅烷)的缩聚,制备了用垂直排列的二氧化硅纳米通道膜修饰的氧化铟锡电极。根据所使用的表面活性剂的不同,它们的孔径在2-3纳米之间。去除表面活性剂后,通过电接枝(即原位生成的氨基苯基单重氮盐的电化学还原)将介孔底部衍生为氨基苯基。这些物质与ITO衬底共价结合,然后通过纳米通道通过苯胺的电聚合来生长聚苯胺纳米丝。在恒电位条件下,通过调整电聚合时间可以控制聚苯胺丝的长度。从溶解二氧化硅模板之前或之后的循环伏安法表征来看,聚苯胺/二氧化硅复合材料和自由聚苯胺纳米线阵列都具有电活性,但由于提供给电解质溶液的有效表面积更大,后者具有更大的峰值电流。在相同电聚合时间下,孔径较大的二氧化硅膜沉积的聚苯胺量较大。所有聚苯胺沉积层均表现出电致变色性质。然而,光谱电化学数据表明,与大体积薄膜相比,纳米丝阵列的有色氧化形式和无色还原聚苯胺之间的相互转换更完全。此外,无模板纳米线阵列(即在二氧化硅溶解后)的电致变色行为比聚苯胺/二氧化硅杂化物更快,证实了这种聚苯胺纳米刷在实际应用中的潜在兴趣。
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来源期刊
Faraday Discussions
Faraday Discussions 化学-物理化学
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期刊介绍: Discussion summary and research papers from discussion meetings that focus on rapidly developing areas of physical chemistry and its interfaces
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