Thermally stable polyimide nanocomposite films from electrospun BaTiO3 fibers for high-density energy storage capacitors

RSC Advances ◽  
2015 ◽  
Vol 5 (56) ◽  
pp. 44749-44755 ◽  
Author(s):  
Yun-Hui Wu ◽  
Jun-Wei Zha ◽  
Zhi-Qiang Yao ◽  
Fang Sun ◽  
Robert K. Y. Li ◽  
...  

PI composite films with electrospun BT fibers were fabricated using the in situ dispersion polymerization method. The microstructures, thermal and dielectric properties of the BT fibers and composite films were investigated.

2020 ◽  
Vol 8 (36) ◽  
pp. 12607-12614 ◽  
Author(s):  
Shuang Xing ◽  
Zhongbin Pan ◽  
Xiaofeng Wu ◽  
Hanxi Chen ◽  
Xujiao Lv ◽  
...  

Composite films with an ultralow filler content of 0.1 vol% Ag-NDs exhibit an excellent high-temperature discharge energy density of 2.56 J cm−3, together with efficiency exceeding 80% at a temperature of 150 °C.


2013 ◽  
Vol 395-396 ◽  
pp. 133-137
Author(s):  
Xing Zhao ◽  
Jin Hua Yin ◽  
Rong Jin ◽  
Jin Yu Dong

Polymer/TiO2 nanocomposite films have good mechanical, electrical and thermal property, which are applied to electrical engineering and microelectronic technique field extensively. Nano-TiO2 has bigger permittivity and better absorption ultraviolet. The PI/TiO2-PI-PI/TiO2 three layer composite films (30mm) with different content and interlayer thickness were prepared via in-situ dispersion polymerization in this paper. And the films with A (5mm), B (10mm) and C (15mm) interlayer PI thickness are divided into three different series. The results show that inorganic TiO2 nanoparticles are well dispersed in the polymer matrices. And the structures of three layers are obvious. The doped nanoparticles don’t affect the imidization of PI matrix in composite films. The time-to-breakdown of all series films increases with the TiO2 content increasing, in which the B series films possess the best performance. Besides, the B series films with 4% doping content are tested with the longest time-to-breakdown, which is three times more than that of pure PI. After corona aging, there are lots of TiO2-particles with the ability of absorbing UV accumulated on the surface of films, playing the role in shielding electric field, which is one factor resulting in improvement of corona-resistance in the composite films.


2010 ◽  
Vol 25 (12) ◽  
pp. 2384-2391 ◽  
Author(s):  
Jun-Wei Zha ◽  
Ben-Hui Fan ◽  
Zhi-Min Dang ◽  
Sheng-Tao Li ◽  
George Chen

Polyimide (PI)-matrix composite films containing inorganic nanoparticles (nano-Al2O3 and nano-TiO2) have been fabricated. A proposed model is used to explain different structures of the (Al2O3–TiO2)/PI (ATP) films synthesized by employing in situ polymerization. Dependences of dielectric permittivities of the ATP films on frequency and temperature were studied. Results show the breakdown strength of the films decreases with prolonging the corona aging time. The incorporation of the nano-Al2O3 and nano-TiO2 particles significantly improves the corona resistance of the films. The corona aging also influences the infrared absorbance, the glass transition temperature (Tg), and loss factor (tanδ) of the ATP films.


2015 ◽  
Vol 41 (10) ◽  
pp. 13582-13588 ◽  
Author(s):  
M. Wang ◽  
W.L. Li ◽  
Y. Feng ◽  
Y.F. Hou ◽  
T.D. Zhang ◽  
...  

Proceedings ◽  
2018 ◽  
Vol 2 (13) ◽  
pp. 1060 ◽  
Author(s):  
Attila Bonyár ◽  
Zsanett Izsold ◽  
Alexandra Borók ◽  
István Csarnovics ◽  
László Himics ◽  
...  

Polydimethylsiloxane (PDMS)–gold/silver nanoparticle composite films were synthetized in situ by using a simple method, which is based on the reduction of chloroauric acid (HAuCl4) or silver nitrate solution (AgNO3) by the PDMS membrane. A method to monitor the development of the plasmonic absorbance peak in situ (during the synthesis of the nanoparticles) is introduced in order to provide a convenient way to investigate the effect of the technological parameters on the position of the resulting peak. The resulting composite films were tested as SERS substrates at two excitation wavelengths (488 nm, 785 nm) and the preliminary results indicate that they are promising candidates for this application, with high sensitivities accompanied by cheap fabrication costs.


Materials ◽  
2019 ◽  
Vol 12 (3) ◽  
pp. 439 ◽  
Author(s):  
Lulu Gu ◽  
Tao Li ◽  
Yongjun Xu ◽  
Chenghua Sun ◽  
Zhenyu Yang ◽  
...  

BaTiO3/polymer/Al (BPA) composite films for energy storage were fabricated by way of a roll coating and thermal curing process. The coating slurry consisted of silicon-containing heat-resistant resin (CYN-01) and BaTiO3 particles with various particle sizes obtained from commercial BaTiO3 powders processed at different durations of wet sand grinding in the presence of silane coupling agent (KH550), which not only improves the dielectric performance of the BPA films but also facilitates its production in a large scale. The major influence factors, such as the ratio between BaTiO3 and resin and the size of BaTiO3 particles, were investigated and their related mechanisms were discussed. The results show that modifying BaTiO3 particles (D90 = 0.83 μm) with the silane coupling agent of KH550 enhances the dielectric properties of the BPA films. The typical BPA films obtained exhibit a high dielectric constant of 32, a high break strength of 20.8 V/μm and a low dielectric loss of 0.014. The present work provides a simple and convenient way to prepare high-quality ceramic/polymer composite films for energy-storage application in a large scale.


2017 ◽  
Vol 29 (23) ◽  
pp. 10206-10211 ◽  
Author(s):  
Zhenguang Wang ◽  
Yuan Xiong ◽  
Stephen V. Kershaw ◽  
Bingkun Chen ◽  
Xuming Yang ◽  
...  

1995 ◽  
Vol 418 ◽  
Author(s):  
M. L. Trudell ◽  
G. Subramanian ◽  
G. Eck ◽  
J. H. Boyer

AbstractAn improved nitration procedure has been developed for the synthesis of y-Tacot (3). The synthesis of y-DBBD (8) has been completed in three steps from 3 in 37% yield. y-DBBD (8) was found to be thermally stable up to 274 °C (decomposed) and insensitive to impact (hammer blow). Nitration of z-BDDB (6) and y-DBBD (8) gave carbonyl derivatives resulting from in situ hydroysis/oxidation of the corresponding tetranitro derivatives z-TBBD (7) and y-TBBD (9), respectively.


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