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Enhanced energy density of PVDF-based nanocomposites via a core–shell strategy
In recent years, high energy density polymer capacitors have attracted a lot of scientific interest due to their potential applications in advanced power systems and electronic devices. Here, core–shell structured TiO(2)@SrTiO(3)@polydamine nanowires (TiO(2)@SrTiO(3)@PDA NWs) were synthesized via a...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7555536/ https://www.ncbi.nlm.nih.gov/pubmed/33051480 http://dx.doi.org/10.1038/s41598-020-73884-6 |
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author | Xu, JingJing Fu, Chao Chu, Huiying Wu, Xianyou Tan, Zhongyang Qian, Jing Li, Weiyan Song, Zhongqian Ran, Xianghai Nie, Wei |
author_facet | Xu, JingJing Fu, Chao Chu, Huiying Wu, Xianyou Tan, Zhongyang Qian, Jing Li, Weiyan Song, Zhongqian Ran, Xianghai Nie, Wei |
author_sort | Xu, JingJing |
collection | PubMed |
description | In recent years, high energy density polymer capacitors have attracted a lot of scientific interest due to their potential applications in advanced power systems and electronic devices. Here, core–shell structured TiO(2)@SrTiO(3)@polydamine nanowires (TiO(2)@SrTiO(3)@PDA NWs) were synthesized via a combination of surface conversion reaction and in-situ polymerization method, and then incorporated into the poly(vinylidene fluoride) (PVDF) matrix. Our results showed that a small amount of TiO(2)@SrTiO(3)@PDA NWs can simultaneously enhance the breakdown strength and electric displacement of nanocomposite (NC) films, resulting in improved energy storage capability. The 5 wt% TiO(2)@SrTiO(3)@PDA NWs/PVDF NC demonstrates 1.72 times higher maximum discharge energy density compared to pristine PVDF (10.34 J/cm(3) at 198 MV/m vs. 6.01 J/cm(3) at 170 MV/m). In addition, the NC with 5 wt% TiO(2)@SrTiO(3)@PDA NWs also demonstrates an excellent charge–discharge efficiency (69% at 198 MV/m). Enhanced energy storage performance is due to hierarchical interfacial polarization among their multiple interfaces, the large aspect ratio as well as surface modification of the TiO(2)@SrTiO(3) NWs. The results of this study provide guidelines and a foundation for the preparation of the polymer NCs with an outstanding discharge energy density. |
format | Online Article Text |
id | pubmed-7555536 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75555362020-10-14 Enhanced energy density of PVDF-based nanocomposites via a core–shell strategy Xu, JingJing Fu, Chao Chu, Huiying Wu, Xianyou Tan, Zhongyang Qian, Jing Li, Weiyan Song, Zhongqian Ran, Xianghai Nie, Wei Sci Rep Article In recent years, high energy density polymer capacitors have attracted a lot of scientific interest due to their potential applications in advanced power systems and electronic devices. Here, core–shell structured TiO(2)@SrTiO(3)@polydamine nanowires (TiO(2)@SrTiO(3)@PDA NWs) were synthesized via a combination of surface conversion reaction and in-situ polymerization method, and then incorporated into the poly(vinylidene fluoride) (PVDF) matrix. Our results showed that a small amount of TiO(2)@SrTiO(3)@PDA NWs can simultaneously enhance the breakdown strength and electric displacement of nanocomposite (NC) films, resulting in improved energy storage capability. The 5 wt% TiO(2)@SrTiO(3)@PDA NWs/PVDF NC demonstrates 1.72 times higher maximum discharge energy density compared to pristine PVDF (10.34 J/cm(3) at 198 MV/m vs. 6.01 J/cm(3) at 170 MV/m). In addition, the NC with 5 wt% TiO(2)@SrTiO(3)@PDA NWs also demonstrates an excellent charge–discharge efficiency (69% at 198 MV/m). Enhanced energy storage performance is due to hierarchical interfacial polarization among their multiple interfaces, the large aspect ratio as well as surface modification of the TiO(2)@SrTiO(3) NWs. The results of this study provide guidelines and a foundation for the preparation of the polymer NCs with an outstanding discharge energy density. Nature Publishing Group UK 2020-10-13 /pmc/articles/PMC7555536/ /pubmed/33051480 http://dx.doi.org/10.1038/s41598-020-73884-6 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Xu, JingJing Fu, Chao Chu, Huiying Wu, Xianyou Tan, Zhongyang Qian, Jing Li, Weiyan Song, Zhongqian Ran, Xianghai Nie, Wei Enhanced energy density of PVDF-based nanocomposites via a core–shell strategy |
title | Enhanced energy density of PVDF-based nanocomposites via a core–shell strategy |
title_full | Enhanced energy density of PVDF-based nanocomposites via a core–shell strategy |
title_fullStr | Enhanced energy density of PVDF-based nanocomposites via a core–shell strategy |
title_full_unstemmed | Enhanced energy density of PVDF-based nanocomposites via a core–shell strategy |
title_short | Enhanced energy density of PVDF-based nanocomposites via a core–shell strategy |
title_sort | enhanced energy density of pvdf-based nanocomposites via a core–shell strategy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7555536/ https://www.ncbi.nlm.nih.gov/pubmed/33051480 http://dx.doi.org/10.1038/s41598-020-73884-6 |
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