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聚(噻吩并[3,4 - b]-1,4 - 氧硫杂环戊烷):对电聚合和电致变色性能有中等影响。

Poly(thieno[3,4-b]-1,4-oxathiane): medium effect on electropolymerization and electrochromic performance.

作者信息

Wang Zhipeng, Xu Jingkun, Lu Baoyang, Zhang Shimin, Qin Leiqiang, Mo Daize, Zhen Shijie

机构信息

Jiangxi Key Laboratory of Organic Chemistry, Jiangxi Science and Technology Normal University , Nanchang 330013, P. R. China.

出版信息

Langmuir. 2014 Dec 30;30(51):15581-9. doi: 10.1021/la503948f. Epub 2014 Dec 17.

Abstract

The asymmetrical sulfur analog of 3,4-ethylenedioxythiophene (EDOT), thieno[3,4-b]-1,4-oxathiane (EOTT), was synthesized, and its electropolymerization was comparatively investigated by employing different solvent-electrolyte systems (room temperature ionic liquid 1-butyl-3-methylimidazolium hexafluorophosphate (BmimPF6), CH2Cl2-Bu4NPF6, and CH2Cl2-BmimPF6). Further, the effect of solvents and supporting electrolytes on the structure, morphology, electrochemical, electronic, and optical properties and electrochromic performance of the obtained poly(thieno[3,4-b]-1,4-oxathiane) (PEOTT) films were minutely studied. PEOTT film with a band gap (Eg) of about 1.6 eV could be facilely electrodeposited in all the solvent-electrolytes and displayed excellent electroactivity, outstanding redox stability in a wide potential window, and improved thermal stability. Cyclic voltammetry showed that EOTT could be electropolymerized at a lower oxidation potential in BmimPF6 (∼1.0 V vs Ag/AgCl) due to several advantanges of RTIL BmimPF6 itself, such as high intrinsic conductivity and mild chemical conditions, etc., and the resulting PEOTT film exhibited compact morphology with better electroactivity and stability and higher electrical conductivity. On the other hand, PEOTT films from all the sovent-electrolytes also showed the electrochromic nature by color changing from gray blue to green, and further kinetic studies revealed that PEOTT had decent contrast ratios (36%), higher coloration efficiencies (212 cm(2)/C in BmimPF6), low switching voltages, moderate response time (1.2 s), excellent stability, and color persistence. From these results, PEOTT provides more plentiful electrochromic colors and holds promise for display applications.

摘要

合成了3,4-亚乙基二氧噻吩(EDOT)的不对称硫类似物噻吩并[3,4-b]-1,4-氧硫杂环戊烷(EOTT),并采用不同的溶剂-电解质体系(室温离子液体1-丁基-3-甲基咪唑六氟磷酸盐(BmimPF6)、CH2Cl2-Bu4NPF6和CH2Cl2-BmimPF6)对其电聚合进行了比较研究。此外,还详细研究了溶剂和支持电解质对所得聚(噻吩并[3,4-b]-1,4-氧硫杂环戊烷)(PEOTT)薄膜的结构、形貌、电化学、电子和光学性质以及电致变色性能的影响。在所有溶剂-电解质中都可以轻松电沉积出带隙(Eg)约为1.6 eV的PEOTT薄膜,该薄膜显示出优异的电活性、在宽电位窗口内出色的氧化还原稳定性以及改善的热稳定性。循环伏安法表明,由于室温离子液体BmimPF6本身的几个优点,如高本征电导率和温和的化学条件等,EOTT在BmimPF6中可以在较低的氧化电位(相对于Ag/AgCl约为1.0 V)下进行电聚合,所得的PEOTT薄膜呈现出致密的形貌,具有更好的电活性和稳定性以及更高的电导率。另一方面,所有溶剂-电解质体系制备的PEOTT薄膜也表现出电致变色性质,颜色从灰蓝色变为绿色,进一步的动力学研究表明,PEOTT具有良好的对比度(36%)、较高的显色效率(在BmimPF6中为212 cm2/C)、低开关电压、适中的响应时间(1.2 s)、优异的稳定性和颜色持久性。从这些结果来看,PEOTT提供了更丰富的电致变色颜色,在显示应用方面具有潜力。

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