scholarly journals Core–shell structured Ag@C nanocables for flexible ferroelectric polymer nanodielectric materials with low percolation threshold and excellent dielectric properties

RSC Advances ◽  
2018 ◽  
Vol 8 (1) ◽  
pp. 1-9 ◽  
Author(s):  
Zhihui Chen ◽  
Hengfeng Li ◽  
Guangyou Xie ◽  
Ke Yang

Flexible Ag@C-NC/PVDF nanocomposite materials with low percolation threshold and dielectric constant of 295 at 1 kHz.

Nanoscale ◽  
2014 ◽  
Vol 6 (24) ◽  
pp. 14740-14753 ◽  
Author(s):  
Ke Yang ◽  
Xingyi Huang ◽  
Lijun Fang ◽  
Jinliang He ◽  
Pingkai Jiang

Fluoro-polymer functionalized graphene was synthesized for flexible polymer-based nanodielectrics. The resulting nanocomposites exhibit high dielectric constant, suppressed dielectric loss and low percolation threshold.


2018 ◽  
Vol 11 (01) ◽  
pp. 1850010 ◽  
Author(s):  
Yuqiang Guo ◽  
Yifei Wang ◽  
Yaxuan Ren ◽  
Mingzhu Fu ◽  
Hongmei Ma ◽  
...  

Based on the percolation threshold theory of conductive-dielectric composites, the dielectric constant can be improved more by adding a certain mass fraction of conductive particle into polymer matrix. However, the dielectric loss increases with the increasing mass fraction of conductive particle. In this paper, conductive Polyaniline (PANI) with different particle sizes is utilized to illustrate that reducing particle size can improve the dielectric properties. The dielectric constant is increased from 319 to 540, and dielectric loss is decreased from 2.34 to 0.85 when PANI with smaller particle size is used. Moreover, PANI coated with an insulating surfactant layer can further improve the dielectric properties, the experimental results show that the dielectric constant of the composite could be more than 1000, while the dielectric loss is 0.35 at 1[Formula: see text]KHz.


RSC Advances ◽  
2016 ◽  
Vol 6 (30) ◽  
pp. 25015-25022 ◽  
Author(s):  
Weng Ling ◽  
Li Hongxia ◽  
Ju Peihai ◽  
Wang Ting ◽  
Liu Lizhu

The dielectric constant of PVDF/TiC@AlOOH nanocomposite films is as high as 1.8 × 107 at 100 Hz.


This chapter sheds light on the recent nanotechnology theoretical models for interphase power law IPL model, inhomogeneous interphase, and multi-nanoparticles technique. Moreover, this chapter reviews deliberate hypothetical researches of the effective dielectric constant for polymer/filler nanocomposites and its reliance on “filler concentration, the interphase interactions, polymer filler dielectric constant, and interphase dielectric constant.” This chapter also investigates the prediction of the dielectric constant of new nanocomposite materials dependent upon exponential power law model. Thus, this work moves from the dielectric properties of beginning polymer matrix forward and predicts the dielectric properties of new nanocomposite materials to be utilized for high voltage and directing materials by adding specified nanoparticles with polymer matrix.


2018 ◽  
Vol 20 (4) ◽  
pp. 2777-2786 ◽  
Author(s):  
Minhao Yang ◽  
Hang Zhao ◽  
Chaohe Hu ◽  
Paul Haghi-Ashtiani ◽  
Delong He ◽  
...  

Core–shell structured TiO2@C nanowires were synthesized and the dielectric properties of the nanocomposites could be largely enhanced after incorporating these core–shell structured nanowires.


2002 ◽  
Vol 718 ◽  
Author(s):  
Dae-Chul Park ◽  
Jun-ichi Itoh ◽  
Isao Sakaguchi ◽  
Naoki Ohashi ◽  
Toyohiko Yano ◽  
...  

AbstractDielectric properties and microstructure were investigated in BaTiO3 ceramics with various additives, Ho2O3, MgO, Ho2O3/MgO, and La2O3. The dielectric constants were increased up to ∼4000 and ∼3000 at 25°C in the 1 mol% Ho-doped and 0.5 mol% Mg-doped BaTiO3 materials, respectively. The BaTiO3 material codoped with 3 mol% Ho + 1.5 mol% Mg led to increase dielectric constant up to ∼6000 at 25°C and the dielectric constant peak around Curie temperature was suppressed at temperature range of from 25°C to 125°C. The size of BaTiO3 grains depended on the content and kind of an additive. Core-shell grains and secondary phase were also dependent on an additive. Core-shell grains were formed completely in Ho-doped BaTiO3 except for 0.5 mol%, but the structure was little observed in Mg- and La-doped BaTiO3 material. Codoped BaTiO3 also formed the core-shell grains.


2020 ◽  
Vol 16 ◽  
Author(s):  
Alliya Qamar ◽  
Rehana Zia ◽  
Madeeha Riaz

Background: Hydroxyapatite is similar to bone mineral in chemical composition, has good biocompatibility with host tissue and bone. Objective: This work aims to tailor the mechanical and dielectric properties of hydroxyapatite with zinc sudstitution, to improve wearability of implant and accelerate the healing process. Method: Pure and zinc incorporated hydroxyapatite Ca10(PO4)6(OH)2 samples have been successfully prepared by means of the chemical precipitation method. Results: The results showed that hydroxyapatite(Hap) having hexagonal structure was the major phase identified in all the samples. It was found that secondary phase of β-tricalcium phosphate (β-TCP) formed due to addition of Zinc resulting in biphasic structure BCP (Hap + β-TCP). A minor phase of ZnO also formed for higher concentration of Zn (Zn ≥ 2mol%) doping. It was found that the Zn incorporation to Hap enhanced both mechanical and dielectric properties without altering the bioactive properties. The microhardness increased upto 0.87 GPa for Zn concentration equal to 1.5mol%, which is comparable to the human bone ~0.3 - 0.9 GPa. The dielectric properties evaluated in the study showed that 1.5 mol% Zn doped hydroxyapatite had highest dielectric constant. Higher values of dielectric constant at low frequencies signifies its importance in healing processes and bone growth due to polarization of the material under the influence of electric field. Conclusion: Sample Z1.5 having 1.5 mol% Zn doping showed the most optimized properties suitable for bone regeneration applications.


Polymers ◽  
2021 ◽  
Vol 13 (15) ◽  
pp. 2451
Author(s):  
Jianwen Zhang ◽  
Dongwei Wang ◽  
Lujia Wang ◽  
Wanwan Zuo ◽  
Lijun Zhou ◽  
...  

To study the effect of hyperbranched polyester with different kinds of terminal groups on the thermomechanical and dielectric properties of silica–epoxy resin composite, a molecular dynamics simulation method was utilized. Pure epoxy resin and four groups of silica–epoxy resin composites were established, where the silica surface was hydrogenated, grafted with silane coupling agents, and grafted with hyperbranched polyester with terminal carboxyl and terminal hydroxyl, respectively. Then the thermal conductivity, glass transition temperature, elastic modulus, dielectric constant, free volume fraction, mean square displacement, hydrogen bonds, and binding energy of the five models were calculated. The results showed that the hyperbranched polyester significantly improved the thermomechanical and dielectric properties of the silica–epoxy composites compared with other surface treatments, and the terminal groups had an obvious effect on the enhancement effect. Among them, epoxy composite modified by the hyperbranched polyester with terminal carboxy exhibited the best thermomechanical properties and lowest dielectric constant. Our analysis of the microstructure found that the two systems grafted with hyperbranched polyester had a smaller free volume fraction (FFV) and mean square displacement (MSD), and the larger number of hydrogen bonds and greater binding energy, indicating that weaker strength of molecular segments motion and stronger interfacial bonding between silica and epoxy resin matrix were the reasons for the enhancement of the thermomechanical and dielectric properties.


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