通过处理后去除侧链,显著提高合聚合物的电导性
James F Ponder1, Shawn A Gregory2, Amalie Atassi2
1George W. Woodruff School of Mechanical Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332, United States.
Journal of the American Chemical Society
|January 10, 2022
概括
通过水解从合聚合物 (CP) 中去除侧链可显著提高电导率. 这一过程提高了电荷载体密度,并减少了局部化,使高级设备能够使用高导电性CP膜.
科学领域:
- 材料科学
- 聚合物化学
- 有机电子
背景情况:
- 结合聚合物 (CP) 对于氧化还原和固态装置至关重要.
- 溶解CP需要侧链,这可以通过减少电活性物质和阻碍相互作用来阻碍性能.
- 尽量减少侧链的影响是优化CP属性的关键.
研究的目的:
- 调查加工后侧链去除对结合聚合物的电导率的影响.
- 了解侧链水解后导电性增强背后的机制.
- 将侧链去除用于高性能共聚物,以提高电子性能.
主要方法:
- 用以除去侧链的化.
- 聚合物膜体积和形态的特征.
- 电化学分析,X射线光电子光谱 (XPS) 和电荷传输建模.
主要成果:
- 侧链水解显著增加了化学化CP薄膜的电导率.
- 导电性增强归因于电荷载体密度的增加和载体局部化的减少,而不是注的增加.
- 对ProDOT-alt-EDOT共聚物的水解产生了高达700S/cm的导电性.
结论:
- 处理后的侧链去除是提高CP导电性的有效策略.
- 这种方法克服了溶解侧链所带来的局限性.
- 该方法可用于各种应用的高导电合聚合物薄膜的溶液处理.
相关概念视频
Anionic Chain-Growth Polymerization: Overview
2.2K
The polymerization process that involves carbanion as an intermediate is called anionic polymerization. It is also a type of addition or chain-growth polymerization. Anionic polymerization gets initiated by a strong nucleophile such as an organolithium or a Grignard reagent. The most commonly used initiator for anionic polymerization is butyl lithium. Monomers involved in anionic polymerization must possess a vinyl group bonded to one or two electron-withdrawing groups. For instance,...
2.2K
Cationic Chain-Growth Polymerization: Mechanism
2.5K
The cationic polymerization mechanism consists of three steps: initiation, propagation, and termination. In the initiation step of the polymerization process, the π bond of a monomer gets protonated by the Lewis acid catalyst, which is formed from boron trifluoride and water. The protonation of the π bond generates a carbocation stabilized by the electron‐donating group. In the propagation step, the π bond of the second monomer acts as a nucleophile and attacks the...
2.5K
Anionic Chain-Growth Polymerization: Mechanism
2.1K
The mechanism for anionic chain-growth polymerization involves initiation, propagation, and termination steps. In the initiation step, a nucleophilic anion, such as butyl lithium, initiates the polymerization process by attacking the π bond of the vinylic monomer. As a result, a carbanion, stabilized by the electron‐withdrawing group, is generated. The resulting carbanion acts as a Michael donor in the propagation step and attacks the second vinylic monomer, which acts as a Michael...
2.1K
Radical Chain-Growth Polymerization: Mechanism
2.8K
The radical chain-growth polymerization mechanism consists of three steps: initiation, propagation, and termination of polymerization. The polymerization initiates when a free radical generated from the radical initiator adds to the unsaturated bond in the monomer. The unpaired electron of the free radical and one π electron in the unsaturated bond creates a σ bond between the free radical and the monomer. As a result, the other π electron in the unsaturated bond converts this...
2.8K
Ziegler–Natta Chain-Growth Polymerization: Overview
3.5K
Ziegler–Natta polymerization is another form of addition or chain‐growth polymerization used for synthesizing linear polymers over branched polymers. The catalyst used for polymerization is the Ziegler–Natta catalyst, named after Karl Ziegler and Giulio Natta, who developed it in 1953. This catalyst is an organometallic complex of titanium tetrachloride and triethyl aluminum, with the active form of the catalyst being an alkyl titanium compound. Using the Ziegler–Natta...
3.5K
Polymer Classification: Architecture
3.1K
Polymers are classified as linear or branched on the basis of their chain architecture. The polymer chains in linear polymers have a long chain-like structure with minimal to no branching at all. Even if a polymer features large substituent groups on the monomer, which appear as branches to the skeleton, it is not considered a branched polymer. A branched polymer contains secondary polymer chains that arise from the main polymer chain. The branching occurs when the polymer growth shifts from...
3.1K


