...
首页> 外文期刊>Macromolecules >Surface-grafted polymers from electropolymerized polythiophene RAFT agent
【24h】

Surface-grafted polymers from electropolymerized polythiophene RAFT agent

机译:电聚合聚噻吩RAFT剂的表面接枝聚合物

获取原文
获取原文并翻译 | 示例
           

摘要

The synthesis of grafted homopolymer and block copolymer films is reported using a surface-initiated reversible addition-fragmentation chain transfer (SI-RAFT) polymerization from electropolymerized polythiophene on indium tin oxide (ITO) and Au electrode surfaces. The polythiophene macro-RAFT agent was electrodeposited by cyclic voltammetry (CV) from thiobenzoate-functionalized terthiophene monomers. The ultrathin films on Au surfaces were investigated using atomic force microscopy (AFM), static contact angle, X-ray photoelectron spectroscopy (XPS), and ellipsometry. On the other hand, the RAFT agent-modified ITO substrate was monitored by UV-vis to track the electropolymerization of the RAFT agent and formation of π-conjugated polymer. Molecular weight (MW) and polydispersity index (PDI) were determined from sacrificial polymerization in solution. AFM imaging revealed typical polymer layer morphology for the films. Investigation of film thicknesses by ellipsometry and AFM profilometry gave comparable results. XPS showed atomic percentages close to expected values, accounting for variations based on component thickness and XPS sensitivity. Diblock copolymer brush formation revealed capabilities of a conventional SI-RAFT procedure using a polythiophene macroinitiator film.
机译:使用表面引发的可逆加成-断裂链转移(SI-RAFT)聚合反应从电聚合的聚噻吩在铟锡氧化物(ITO)和金电极表面上合成了接枝均聚物和嵌段共聚物薄膜。通过循环伏安法(CV)从硫代苯甲酸酯官能化的对噻吩单体中电沉积聚噻吩大分子RAFT剂。使用原子力显微镜(AFM),静态接触角,X射线光电子能谱(XPS)和椭偏仪研究了Au表面的超薄膜。另一方面,通过UV-vis监测RAFT剂改性的ITO基材,以追踪RAFT剂的电聚合和π-共轭聚合物的形成。分子量(MW)和多分散指数(PDI)由溶液中的牺牲聚合确定。原子力显微镜成像揭示了薄膜的典型聚合物层形态。通过椭圆偏振光度法和AFM轮廓分析法对膜厚度的研究给出了可比较的结果。 XPS的原子百分比接近预期值,这说明了基于组件厚度和XPS灵敏度的变化。二嵌段共聚物刷的形成揭示了使用聚噻吩大分子引发剂膜的常规SI-RAFT方法的能力。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号