Significantly enhanced breakdown field for core-shell structured poly(vinylidene fluoride-hexafluoropropylene)/TiO2 nanocomposites for ultra-high energy density capacitor applications

2018 ◽  
Vol 124 (15) ◽  
pp. 154103 ◽  
Author(s):  
Chenchen Wang ◽  
Jinxi Zhang ◽  
Shaobo Gong ◽  
Kailiang Ren
2018 ◽  
Vol 6 (47) ◽  
pp. 24367-24377 ◽  
Author(s):  
Jie Chen ◽  
Yifei Wang ◽  
Xinwei Xu ◽  
Qibin Yuan ◽  
Yujuan Niu ◽  
...  

A multilayered film is capable of an ultra-high energy density of 20.9 J cm−3 with an efficiency of 72%, outperforming the current ferroelectric polymers.


2020 ◽  
Vol 13 (06) ◽  
pp. 2051042
Author(s):  
Zhong Yang ◽  
Jing Wang ◽  
Long He ◽  
Chaoyong Deng ◽  
Kongjun Zhu

Flexible dielectric capacitors are becoming shining stars in modern electronic devices. Ceramic particles with large dielectric constants and benign compatibility are attractive candidates to enhance the energy storage density of pristine polymer capacitors while guaranteeing their flexibility. In this work, double-shell structure of Al2O3 (AO) and dopamine (PDA) were successively coated on the Nd-doped BaTiO3 (NBT) particles and then introduced into the Poly(vinylidene fluoride) (PVDF) matrix. Obvious enhancement in dielectric constants was observed while the dielectric loss remained nearly constant. For the composite films with 1–4[Formula: see text]vol.% NBT@AO@PDA NPs, the maximum energy density of 9.1[Formula: see text]J/cm3 and energy efficiency of 65% was achieved at 430[Formula: see text]MV/m in the sample with 1[Formula: see text]vol.% filling ratio, which are 1.4 and 1.3 times larger than those of pristine PVDF at 450[Formula: see text]MV/m. The finite element simulation reveals the effective relief of the electric field concentration in the composite film induced by the AO and PDA layers. The greater improvement in the energy storage performance could be anticipated if the dispersity of NBT@AO@PDA NPs was further improved.


RSC Advances ◽  
2016 ◽  
Vol 6 (2) ◽  
pp. 1589-1599 ◽  
Author(s):  
Honghong Gong ◽  
Bei Miao ◽  
Xiao Zhang ◽  
Junyong Lu ◽  
Zhicheng Zhang

The antiferroelectric-like behavior could be retained up to 675 MV m−1 with a discharged energy density of 23.3 J cm−3 because of the confinement of rigid PMMA segment onto the ferroelectric relaxation of P(VDF-TrFE-CTFE) and the high breakdown strength.


2020 ◽  
Vol 10 (1) ◽  
Author(s):  
JingJing Xu ◽  
Chao Fu ◽  
Huiying Chu ◽  
Xianyou Wu ◽  
Zhongyang Tan ◽  
...  

Abstract 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 TiO2@SrTiO3@polydamine nanowires (TiO2@SrTiO3@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 TiO2@SrTiO3@PDA NWs can simultaneously enhance the breakdown strength and electric displacement of nanocomposite (NC) films, resulting in improved energy storage capability. The 5 wt% TiO2@SrTiO3@PDA NWs/PVDF NC demonstrates 1.72 times higher maximum discharge energy density compared to pristine PVDF (10.34 J/cm3 at 198 MV/m vs. 6.01 J/cm3 at 170 MV/m). In addition, the NC with 5 wt% TiO2@SrTiO3@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 TiO2@SrTiO3 NWs. The results of this study provide guidelines and a foundation for the preparation of the polymer NCs with an outstanding discharge energy density.


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