存水弯(水管)
X射线光电子能谱
材料科学
纳米复合材料
俘获
聚合物
偶极子
聚乙烯
电荷(物理)
聚合物纳米复合材料
表面电荷
化学物理
分析化学(期刊)
纳米技术
分子物理学
复合材料
化学工程
化学
物理化学
物理
有机化学
工程类
气象学
色谱法
生态学
生物
量子力学
作者
Haruto Suzuki,Yugo Kubo,Yoitsu Sekiguchi,Masaki Kobayashi,Akiko Kumada,Masahiro Sato
标识
DOI:10.1088/1361-6463/acd1fa
摘要
Abstract Polymer nanocomposites (PNCs) exhibit excellent electrical properties owing to charge trapping provided by nanofillers. However, the role of nanofillers in trap formation at the microscopic level is poorly understood. In this study, we propose a method to determine the charge trap depth of nanofillers in PNCs using x-ray photoelectron spectroscopy (XPS) measurements and first-principles calculations. The low-density polyethylene (PE)/TiO 2 nanocomposite is selected as the measurement target as it was previously reported the charges are trapped by TiO 2 loading to PE. We observe TiO 2 can serve as a trap for holes, and the trap depth is determined to be 0.9 eV. Furthermore, the computed charge trap depth calculated by G 0 W 0 calculation, which reproduce the experimental band gap, is comparable to the XPS result, which strongly supports the validity of our method. In addition, owing to the quantitative evaluation of the electronic structure, it was shown that the charge trap depth of the nanofiller can be controlled by tuning the surface dipole with surface modification of the nanofiller. The approach proposed in this study to determine the charge trap depth of nanofillers provides the prospect of designing PNCs with desirable properties from the atomic or molecular level.
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