俘获
电介质
复合数
电荷(物理)
材料科学
接口(物质)
化学物理
聚合物
复合材料
凝聚态物理
纳米技术
光电子学
化学
物理
量子力学
生物
生态学
毛细管作用
毛细管数
作者
Haoxiang Zhao,Lixuan An,Daning Zhang,Xiong Yang,Huanmin Yao,Guanjun Zhang,Haibao Mu,Björn Baumeier
标识
DOI:10.1021/acs.jpcb.4c08661
摘要
Interface design is a promising strategy to enhance the dielectric strength in polymer composites through regulating the charge transport process. However, the targeted exploitation of interface effects is limited due to a lack of fundamental understanding of the underlying mechanisms involving elementary electronic processes and details of the intricate interplay of characteristics of molecular building blocks and the interfacial morphology - details that cannot fully be resolved with experimental methods or commonly used band transport models. Here, we instead build a proper theoretical framework for polymer dielectrics based on charge hopping and employ a multiscale modeling approach linking the quantum properties of the charge carriers with nano- and mesoscale structural details of complex interfaces. Applied to a prototypical application-proven cellulose-oil interface system, this approach demonstrates that charges are trapped in the disordered region. Specifically, it unveils this trapping as a synergistic effect of two transport-regulating interface mechanisms: back-transfer to the oil region is suppressed by energetic factors, while forward-transfer to the crystalline cellulose is suppressed by low electronic coupling. The insight into the molecular origins of interface effects via dual-interface regulation in the framework of charge hopping offers new development paths for developing advanced energy materials with tailored electrical properties.
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