高循环TiO2/PANI电致变色薄膜的制备与性能表征

Preparation and property characterisation of high cycle TiO2/PANI electrochromic thin films

  • 摘要: 基于电致变色薄膜在军事伪装、建筑节能、汽车工业等领域具有广泛应用前景,研究采用化学氧化法制备TiO2/聚苯胺(PANI)复合材料。利用XRD、FTIR、SEM、XPS、TG、UV-vis、电化学工作站对制备的TiO2/PANI电极与PANI电极进行测试分析,重点研究TiO2/PANI复合薄膜和PANI薄膜的结构形貌、电化学性能及电致变色性能的变化机制。结果表明:TiO2/PANI复合薄膜具有供体受体结构,相较于PANI 薄膜纤维状结构有更多的活性位点;TiO2/PANI复合薄膜的结构加快PANI质子化和脱质子化的转变进程,改善电荷转移途径,缩短离子扩散路径,延缓变色过程中PANI的氧化降解; TiO2/PANI复合薄膜较PANI薄膜的电致变色性能得到提升,波长650 nm处的着色效率(CE)为 48.52 cm2·C−1,褪色、着色响应时间(τbc)分别为2.5 s、3.0 s,经800次着色褪色循环后薄膜电化学活性保持在初始的71.1%左右。

     

    Abstract: Given the extensive prospective applications of electrochromic thin films in fields such as military camouflage, building energy efficiency, and the automotive industry, this study was conducted to prepare TiO2/Polyaniline (PANI) composites via a chemical oxidation method. The prepared TiO2/PANI electrodes and PANI electrodes were tested and analysed using XRD, FTIR, SEM, XPS, TG, UV-vis and electrochemical workstations. The focus was on the study of the structural morphology, electrochemical properties, and the mechanism of the changes in the electrochromic properties of TiO2/PANI composite films and PANI films. The results demonstrate that the TiO2/PANI composite film exhibits a donor-acceptor structure with a greater number of active sites compared to that of the PANI film, which has a fibrous structure; the structure of TiO2/PANI composite films accelerates the transformation process of PANI protonation and deprotonation, improves the charge transfer pathway, shortens the ion diffusion pathway, and slows down the oxidative degradation of PANI in the process of electrochromic change; the structure of TiO2/PANI composite films is better than PANI films in the process of electrochromic change. The electrochromic performance of the composite film was enhanced in comparison to that of the PANI film, with a colouring efficiency (CE) at wavelength 650 nm of 48.52 cm2·C−1. Additionally, the fading and colouring response times were 2.5 and 3 seconds, respectively. The electrochemical activity of the film was maintained at approximately 71.1% of the initial value after 800 cycles of colouring and fading.

     

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