Improving the Charge Conductance of Elemental Sulfur via Tandem Inverse Vulcanization and Electropolymerization

被引:58
作者
Dirlam, Philip T. [1 ]
Simmonds, Adam G. [1 ]
Shallcross, R. Clayton [1 ]
Arrington, Kyle J. [1 ]
Chung, Woo Jin [1 ]
Griebel, Jared J. [1 ]
Hill, Lawrence J. [1 ]
Glass, Richard S. [1 ]
Char, Kookheon [2 ]
Pyun, Jeffrey [1 ,2 ]
机构
[1] Univ Arizona, Dept Chem & Biochem, Tucson, AZ 85721 USA
[2] Natl Creat Res Initiat Ctr Intelligent Hybrids, Sch Chem & Biol Engn, Seoul 151744, South Korea
基金
美国国家科学基金会;
关键词
INDIUM TIN OXIDE; CROSS-LINKING; POLYMER; FILMS; NANOPARTICLES; MONOMER;
D O I
10.1021/mz500730s
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The synthesis of polymeric materials using elemental sulfur (S8) as the chemical feedstock has recently been developed using a process termed inverse vulcanization. The preparation of chemically stable sulfur copolymers was previously prepared by the inverse vulcanization of S-8 and 1,3-diisopropenylbenzene (DIB); however, the development of synthetic methods to introduce new chemical functionality into this novel class of polymers remains an important challenge. In this report the introduction of polythiophene segments into poly(sulfur-random-1,3-diisopropenylbenzene) is achieved by the inverse vulcanization of S-8 with a styrenic functional 3,4-propylenedioxythiophene (ProDOT-Sty) and DIB, followed by electropolymerization of ProDOT side chains. This methodology demonstrates for the first time a facile approach to introduce new functionality into sulfur and high sulfur content polymers, while specifically enhancing the charge conductivity of these intrinsically highly resistive materials.
引用
收藏
页码:111 / 114
页数:4
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