电场
聚合物
极化率
化学物理
偶极子
化学
合理设计
单体
缩放比例
纳米技术
工作(物理)
材料科学
分子
有机化学
物理
热力学
量子力学
数学
几何学
作者
Mark A. Rothermund,Stephen J. Koehler,Valerie Vaissier Welborn
出处
期刊:Chemical Reviews
[American Chemical Society]
日期:2024-11-25
卷期号:124 (23): 13331-13369
被引量:17
标识
DOI:10.1021/acs.chemrev.4c00490
摘要
Polymer-based electronic devices are limited by slow transport and recombination of newly separated charges. Built-in electric fields, which arise from compositional gradients, are known to improve charge separation, directional charge transport, and to reduce recombination. Yet, the optimization of these fields through the rational design of polymeric materials is not prevalent. Indeed, polymers are disordered and generate nonuniform electric fields that are hard to measure, and therefore, hard to optimize. Here, we review work focusing on the intentional optimization of electric fields in polymeric systems with applications to catalysis, energy conversion, and storage. This includes chemical tuning of constituent monomers, linkers, morphology, etc. that result in stronger molecular dipoles, polarizability or crystallinity. We also review techniques to characterize electric fields in polymers and emerging processing strategies based on electric fields. These studies demonstrate the benefits of optimizing electric fields in polymers. However, rational design is often restricted to the molecular scale, deriving new pendants on, or linkers between, monomers. This does not always translate in strong electric fields at the polymer level, because they strongly depend on the monomer orientation. A better control of the morphology and monomer-to-polymer scaling relationship is therefore crucial to enhance electric fields in polymeric materials.
科研通智能强力驱动
Strongly Powered by AbleSci AI