Abstract

The dielectric capacitor has been widely used in advanced electronic and electrical power systems due to its capability of ultrafast charging-discharging and ultrahigh power density. Nevertheless, its energy density is still limited by the low dielectric constant(≈ 2.2) of the commercial dielectric polypropylene (PP). The conventional enhancement strategy by embedding inorganic fillers in PP matrix is still difficult and challenging due to that PP hardly dissolves in any inorganic/organic solvent. In this work, we develop a new strategy including freeze-drying, surface functionalization, and hot-pressing to incorporate Ti0.87O2 monolayers in PP film. A series of uniform composited Ti0.87O2@PP film has been successfully fabricated with Ti0.87O2 content range of 0–15 wt%. The maximum dielectric constant of the as-prepared Ti0.87O2@PP film is 3.27 when the Ti0.87O2 content is 9 wt%, which is about 1.5 times higher than that of pure PP. Our study provides a feasible strategy to embed two-dimensional material into commercial PP thin-film with superior dielectric performance for practical application.

Details

Title
Freeze-drying and hot-pressing strategy to embed two-dimensional Ti0.87O2 monolayers in commercial polypropylene films with enhanced dielectric properties
Author
Tian Wenchao 1 ; Yan, Fei 2 ; Cai Cailing 1 ; Wu Zeyi 1 ; Zhang, Chenchen 3 ; Yin Ting 2 ; Lao Sijia 2 ; Hu Linfeng 1 

 Fudan University, Department of Materials Science, Shanghai, China (GRID:grid.8547.e) (ISNI:0000 0001 0125 2443) 
 China Electric Power Research Institute, Beijing, China (GRID:grid.433158.8) (ISNI:0000 0000 8891 7315) 
 State Grid Anhui Electric Power Institute, Hefei, China (GRID:grid.8547.e) 
Pages
368-376
Publication year
2021
Publication date
Apr 2021
Publisher
Tsinghua University Press
ISSN
22264108
e-ISSN
22278508
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2497365524
Copyright
© The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.