Electric field assisted assembly of 1D supramolecular nanofibres for enhanced supercapacitive performance

2020 ◽  
Vol 8 (26) ◽  
pp. 13106-13113
Author(s):  
Suman Kundu ◽  
Subi J. George ◽  
Giridhar U. Kulkarni

Supramolecular nanofibres aligned by applying an external AC electric field for enhancing the energy storage performance of a planar supercapacitor.

2021 ◽  
Author(s):  
Ahmed H Biby ◽  
Basant A. Ali ◽  
Nageh Allam

Intercalation of alkali metals has proved to be an effective approach for the enhancement of the energy storage performance in layered-2D materials. However, the research so far has been limited...


2019 ◽  
Vol 31 (3) ◽  
pp. 979-990 ◽  
Author(s):  
Pan Gao ◽  
Zenghui Liu ◽  
Nan Zhang ◽  
Hua Wu ◽  
Alexei A. Bokov ◽  
...  

Materials ◽  
2019 ◽  
Vol 12 (1) ◽  
pp. 119 ◽  
Author(s):  
Bijun Fang ◽  
Yan Jiang ◽  
Xiangyong Zhao ◽  
Shuai Zhang ◽  
Dun Wu ◽  
...  

Antiferroelectric analogous (Pb0.92Sr0.05La0.02)(Zr0.7Sn0.25Ti0.05)O3 (PSLZSnT) ceramics were prepared by the solid-state sintering method by introducing a Y2O3-coating via the self-combustion method. The synthesized Y2O3-doped PSLZSnT ceramics present pseudo-cubic structure and rather uniform microstructural morphology accompanied by relatively small grain size. Excellent energy-storage performance is obtained in the Y2O3-doped PSLZSnT ceramics, in which the value of the energy-storage density presents a linearly increasing trend within the electric field measurement range. Such excellent performance is considered as relating to the rather pure perovskite structure, high relative density accompanied by relatively small grain size, and the antiferroelectric-like polarization-electric field behavior.


2018 ◽  
Vol 6 (21) ◽  
pp. 9823-9832 ◽  
Author(s):  
Jie Yin ◽  
Yuxing Zhang ◽  
Xiang Lv ◽  
Jiagang Wu

Enhancement in energy-storage performance with a recoverable energy density of 2.42 J cm−3 in {Bi0.5[(Na0.8K0.2)0.90Li0.10]0.5}0.96Sr0.04(Ti0.975Ta0.025)O3 ceramics by a hot-pressed sintering (HPS) method.


Nanoscale ◽  
2020 ◽  
Vol 12 (16) ◽  
pp. 8958-8968
Author(s):  
Bingzhong Shen ◽  
Yong Li ◽  
Ningning Sun ◽  
Ye Zhao ◽  
Xihong Hao

The energy-storage performance of an all-inorganic flexible antiferroelectric thin film capacitor is enhanced via constructing a fresh bilayer-like structure.


Author(s):  
Jing Li ◽  
Li Jin ◽  
Ye Tian ◽  
Chao Chen ◽  
Yu Lan ◽  
...  

2018 ◽  
Vol 08 (06) ◽  
pp. 1850039 ◽  
Author(s):  
Bing Xie ◽  
Ling Zhang ◽  
Mohsin Ali Marwat ◽  
Yiwei Zhu ◽  
Weigang Ma ◽  
...  

The development of advanced dielectric film materials with high energy storage performance is of critical significance for pulsed power capacitor applications. Nevertheless, the low discharged energy density ([Formula: see text]) of current dielectric film material restricts their further application. In this work, core-shell structured SrTiO3@SiO2 nanowires (ST@SiO2 NWs) fillers are fabricated based on interface engineering for high [Formula: see text]. The optimized SiO2 insulating layer could effectively confine the mobility of space charge carriers in the interfacial zone between ST NWs and thick SiO2 insulating layer, thus reducing the interfacial polarization between the interface of nanofillers/polymer, which could be used to optimize the electric field strength and electric displacement of the corresponding nanocomposite. As a result, this nanocomposite film simultaneously exhibits enhanced maximum applied electric field ([Formula: see text]) and ([Formula: see text]-[Formula: see text]) values, thus releasing an ultrahigh discharged energy density of 14.7[Formula: see text]J/cm3 at 390[Formula: see text]MV/m, which is 99% higher than that of the conventional ST/P(VDF-CTFE) (without SiO2 coating) nanocomposite, and it is almost 2.5 times that of pure P(VDF-CTFE). This work demonstrates the superiority of the core-shell structured paraelectric nanowire in enhancing the energy storage performance of dielectric film capacitors, which is expected to guide the design of advanced energy-storage nanocomposites.


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