{"title":"聚苯胺薄膜的电沉积与表征","authors":"Y. Mohd, R. Ibrahim, M. Zainal","doi":"10.1109/SHUSER.2012.6268811","DOIUrl":null,"url":null,"abstract":"This study describes the effects of deposition potential and deposition time on the electrodeposition of Polyaniline (PANi) films on indium tin oxide (ITO)-coated glass substrate. It was found that the aniline with 0.5M in 1M H2SO4 started to polymerize on ITO substrate at + 0.70 V vs Ag/AgCl. Chronoamperometry was used to deposit PANi on ITO-coated glass at three different applied potentials (ie: +0.75V, +1.0V and +1.5V) and three different deposition times (ie: 60s, 300s and 600s). The surface morphology of the PANi films was imaged by field emission scanning electron microscopy (FESEM). The films electrodeposited at different potential and different deposition time exhibit different surface morphologies. At short deposition time (60s) with constant potential of +0.75V, a thin two dimensional (2D) PANi film was deposited on the ITO and adhered strongly on the ITO surface. However, when the deposition time was prolonged longer, the microgranular and nanorod-shaped PANI particles started growing upward on the first layer (thin compact film) and finally the uppermost layer consisted of compact and dense nano-fibrillar PANi particles with few small voids. Nevertheless, the top layer was not strongly adhered on the adherent thin film. On the other hand, deposition at high potential (+1.50V) for a short time also produced a thick and dense PANi layer (dark blue in colour) was formed on the ITO surface with the presence of few voids and crevices. The electrodeposition of Polyaniline (PANi) at +1.50 V was 2.5 times faster than at +1.0V and 23 times faster than at +0.75V. The thin compact PANi film is a promising material to be used in electrochromic windows due to its good adhesion, transparency and electrochromism.","PeriodicalId":426671,"journal":{"name":"2012 IEEE Symposium on Humanities, Science and Engineering Research","volume":"238 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2012-06-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"16","resultStr":"{\"title\":\"Electrodeposition and characterization of Polyaniline films\",\"authors\":\"Y. Mohd, R. Ibrahim, M. Zainal\",\"doi\":\"10.1109/SHUSER.2012.6268811\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"This study describes the effects of deposition potential and deposition time on the electrodeposition of Polyaniline (PANi) films on indium tin oxide (ITO)-coated glass substrate. It was found that the aniline with 0.5M in 1M H2SO4 started to polymerize on ITO substrate at + 0.70 V vs Ag/AgCl. Chronoamperometry was used to deposit PANi on ITO-coated glass at three different applied potentials (ie: +0.75V, +1.0V and +1.5V) and three different deposition times (ie: 60s, 300s and 600s). The surface morphology of the PANi films was imaged by field emission scanning electron microscopy (FESEM). The films electrodeposited at different potential and different deposition time exhibit different surface morphologies. At short deposition time (60s) with constant potential of +0.75V, a thin two dimensional (2D) PANi film was deposited on the ITO and adhered strongly on the ITO surface. However, when the deposition time was prolonged longer, the microgranular and nanorod-shaped PANI particles started growing upward on the first layer (thin compact film) and finally the uppermost layer consisted of compact and dense nano-fibrillar PANi particles with few small voids. Nevertheless, the top layer was not strongly adhered on the adherent thin film. On the other hand, deposition at high potential (+1.50V) for a short time also produced a thick and dense PANi layer (dark blue in colour) was formed on the ITO surface with the presence of few voids and crevices. The electrodeposition of Polyaniline (PANi) at +1.50 V was 2.5 times faster than at +1.0V and 23 times faster than at +0.75V. The thin compact PANi film is a promising material to be used in electrochromic windows due to its good adhesion, transparency and electrochromism.\",\"PeriodicalId\":426671,\"journal\":{\"name\":\"2012 IEEE Symposium on Humanities, Science and Engineering Research\",\"volume\":\"238 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2012-06-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"16\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"2012 IEEE Symposium on Humanities, Science and Engineering Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1109/SHUSER.2012.6268811\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"2012 IEEE Symposium on Humanities, Science and Engineering Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/SHUSER.2012.6268811","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 16
摘要
研究了沉积电位和沉积时间对聚苯胺(PANi)薄膜在氧化铟锡(ITO)镀膜玻璃基板上电沉积的影响。结果表明,在+ 0.70 V /Ag /AgCl条件下,在1M H2SO4中加入0.5M的苯胺在ITO衬底上开始聚合。采用计时电流法在三种不同的应用电位(+0.75V, +1.0V和+1.5V)和三种不同的沉积时间(60s, 300s和600s)下在ito镀膜玻璃上沉积聚苯胺。利用场发射扫描电子显微镜(FESEM)对聚苯胺薄膜的表面形貌进行了成像。在不同电势和不同沉积时间下沉积的薄膜表面形貌不同。在+0.75V恒定电位下,在短时间(60s)内沉积了一层薄薄的二维聚苯胺薄膜,并牢固地粘附在ITO表面。然而,随着沉积时间的延长,第一层(致密薄膜)上开始向上生长微颗粒和纳米棒状的聚苯胺颗粒,最后最上层由致密致密的纳米纤维状聚苯胺颗粒组成,几乎没有小的空隙。然而,顶层在粘附薄膜上的粘附不强。另一方面,在高电位(+1.50V)下短时间沉积也会在ITO表面形成厚而致密的聚苯胺层(颜色为深蓝色),并且几乎没有空洞和缝隙。聚苯胺(PANi)在+1.50 V下的电沉积速度比+1.0V快2.5倍,比+0.75V快23倍。聚苯胺薄膜具有良好的附着力、透明性和电致变色性,是一种很有前途的电致变色窗材料。
Electrodeposition and characterization of Polyaniline films
This study describes the effects of deposition potential and deposition time on the electrodeposition of Polyaniline (PANi) films on indium tin oxide (ITO)-coated glass substrate. It was found that the aniline with 0.5M in 1M H2SO4 started to polymerize on ITO substrate at + 0.70 V vs Ag/AgCl. Chronoamperometry was used to deposit PANi on ITO-coated glass at three different applied potentials (ie: +0.75V, +1.0V and +1.5V) and three different deposition times (ie: 60s, 300s and 600s). The surface morphology of the PANi films was imaged by field emission scanning electron microscopy (FESEM). The films electrodeposited at different potential and different deposition time exhibit different surface morphologies. At short deposition time (60s) with constant potential of +0.75V, a thin two dimensional (2D) PANi film was deposited on the ITO and adhered strongly on the ITO surface. However, when the deposition time was prolonged longer, the microgranular and nanorod-shaped PANI particles started growing upward on the first layer (thin compact film) and finally the uppermost layer consisted of compact and dense nano-fibrillar PANi particles with few small voids. Nevertheless, the top layer was not strongly adhered on the adherent thin film. On the other hand, deposition at high potential (+1.50V) for a short time also produced a thick and dense PANi layer (dark blue in colour) was formed on the ITO surface with the presence of few voids and crevices. The electrodeposition of Polyaniline (PANi) at +1.50 V was 2.5 times faster than at +1.0V and 23 times faster than at +0.75V. The thin compact PANi film is a promising material to be used in electrochromic windows due to its good adhesion, transparency and electrochromism.