scholarly journals A Self-healing Hydrogel Electrolyte Towards All-in-one Flexible Supercapacitors

Author(s):  
Wen-Bin Ma ◽  
Ke-Hu Zhu ◽  
Shi-Fang Ye ◽  
Yao Wang ◽  
Lin Guo ◽  
...  

Abstract The autonomously self-healable all-in-one supercapacitor is prepared by in situ rapid polymerization of electrode materials on the surface of self-healing poly (vinyl alcohol) (PVA) hydrogel electrolyte containing sulphuric acid (H2SO4). The self-healing PVA electrolyte has been achieved by physical interaction, in which dynamic hydrogen bonds between PVA chains can readily break and reform, allowing PVA hydrogel electrolyte to self-heal and regain its mechanical and electrochemical properties. The obtained PVA hydrogel displays fast self-healing capability, reliable mechanical performance (stress at 290 KPa after stretching to 238 %) and high ionic conductivity (57.8 mS cm− 1). Based on these excellent properties, an all-in-one supercapacitor with self-healing characteristics is assembled by in situ polymerization of aniline on the surface of self-healable PVA electrolyte. The self-healable all-in-one supercapacitor exhibits specific capacitance 470 mF cm− 2 at current density of 0.2 mA cm− 2 and energy density 32 µWh cm− 2 at power density 100 µW cm− 2. The broken device can be repaired itself and there is a 63% capacitance retention for the healable supercapacitor. This self-healing supercapacitor will promote the development of self-healing energy storage devices in wearable electronics.

Polymers ◽  
2020 ◽  
Vol 12 (9) ◽  
pp. 1918 ◽  
Author(s):  
Hyeong-Jun Jeoung ◽  
Kun Won Kim ◽  
Yong Jun Chang ◽  
Yong Chae Jung ◽  
Hyunchul Ku ◽  
...  

The mechanically-enhanced urea-formaldehyde (UF) microcapsules are developed through a multi-step in situ polymerization method. Optical microscope (OM) and field emission scanning electron microscope (FE-SEM) prove that the microcapsules, 147.4 μm in diameter with a shell thickness of 600 nm, are well-formed. From 1H-nuclear magnetic resonance (1H-NMR) analysis, we found that dicyclopentadiene (DCPD), a self-healing agent encapsulated by the microcapsules, occupies ca. 40.3 %(v/v) of the internal volume of a single capsule. These microcapsules are mixed with EPDM (ethylene-propylene-diene-monomer) and Grubbs’ catalyst via a solution mixing method, and universal testing machine (UTM) tests show that the composites with mechanically-enhanced microcapsules has ca. 47% higher toughness than the composites with conventionally prepared UF microcapsules, which is attributed to the improved mechanical stability of the microcapsule. When the EPDM/microcapsule rubber composites are notched, Fourier-transform infrared (FT-IR) spectroscopy shows that DCPD leaks from the broken microcapsule to the damaged site and flows to fill the notched valley, and self-heals as it is cured by Grubbs’ catalyst. The self-healing efficiency depends on the capsule concentration in the EPDM matrix. However, the self-healed EPDM/microcapsule rubber composite with over 15 wt% microcapsule shows an almost full recovery of the mechanical strength and 100% healing efficiency.


2012 ◽  
Vol 1417 ◽  
pp. 1-13
Author(s):  
Vineela D. Gandham ◽  
Alice B.W. Brochu ◽  
William M. Reichert

2019 ◽  
Vol 361 ◽  
pp. 897-907 ◽  
Author(s):  
Jingchun Lv ◽  
Peiwen Zhou ◽  
Linping Zhang ◽  
Yi Zhong ◽  
Xiaofeng Sui ◽  
...  

2019 ◽  
Vol 2019 ◽  
pp. 1-17
Author(s):  
M. A. Domínguez-Crespo ◽  
A. B. López-Oyama ◽  
A. M. Torres-Huerta ◽  
A. R. Hernández-Basilio ◽  
D. Palma-Ramírez ◽  
...  

In this work, hybrid composites were prepared using polyaniline (PANI) and electrochemically reduced graphene oxide (ERGO) by in situ polymerization. ERGO powders were obtained by a two-way route, Hummer’s method, and one-step potential (−2 V) followed by annealing process at 400°C (TERGO powders): different quantities of TERGO fine particles (10, 20, and 30 wt%) were added to the in situ PANI polymerization in order to produce the hybrid composites. The morphology and structure of the PANI/TERGO compounds were characterized by Raman spectroscopy, ultraviolet-visible spectroscopy (UV-Vis), X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy, scanning electron microscopy (SEM), and transmission electron microscopy (TEM). Thermal treatment of ERGO powders pointed out high-defect surfaces with a wrinkle-type morphology (ID/IG ratio~0.90). The emeraldine phase of PANI was obtained with a maximum value of 61%, which decreases with the amount of TERGO powders. It is also seen that composites displayed a combined morphology between PANI matrix and TERGO powders, confirming a physical interaction between both morphologies. The amount of TERGO particles into the polymeric matrix also modifies the sample microstructure from a semispherical shape to extend sheets, where PANI is sandwiched between TERGO layers. Electrical conductivity of composites slightly increases independent of the TERGO amount (30 S/m and 39 S/m) due to the rough TERGO surface that conditioned the homogeneous nucleation of a large amount of polymer (PANI) reducing the area to move the electrical charge.


2012 ◽  
Vol 713 ◽  
pp. 121-126
Author(s):  
A. Alfonso ◽  
J. Andrés ◽  
J.A. García

The present research work assesses the manufacture of long fiber thermoplastic matrix composite materials (GreenComposites). Thermoplastic matrices are too viscous to be injected into the conventional LCM (Liquid Composite Molding) molds, and then epoxy, polyester or vinylester resins are used. Nevertheless, the groundbreaking anionic polymerization of caprolactam allows such a synthesis of a thermoplastic APA6 matrix inside the mold. This matrix is sintered from the starting monomers, and presents high mechanical performance and recyclability. In order to do the reactive injection in a LCM mold, it is necessary to control the polymerization mechanism of such a thermoplastic matrix. This paper puts special emphasis on detecting and solving all problems which arose during synthesis. For instance, moisture values were assessed for all starting reactants, since humidity keeps polymerization from occurring. It is thought that once the synthesis and the resulting material characterization are well controlled, the manufacture of GreenComposites through in situ polymerization, as well as addition of state-of-the-art fabrics such as basalt, can proceed successfully.


2010 ◽  
Vol 148-149 ◽  
pp. 1031-1035
Author(s):  
Yang Zhao ◽  
Wei Zhang ◽  
Le Ping Liao ◽  
Wu Jun Li ◽  
Yi Xin

With the development of the embedded microcapsule concept for self-healing material, the preparation of microcapsule has been paid more attentions. A new series of microcapsules were prepared by in situ polymerization technology in an oil-in-water emulsion with polyoxymethylene urea (PMU) as shell material and a mixture of epoxy resins as core material. The PMU microcapsules were characterized by Fourier transform infrared spectroscopy (FTIR), scanning electronic microscopy (SEM), particle size analyzer and thermo gravimetric analyzer (TGA) to investigate their chemical structure, surface morphology, size distribution and thermal stability, respectively. The results indicate that PMU microcapsules containing epoxy resins can be synthesized successfully. The optimized reaction parameters were obtained as follow: agitation rate 600 rpm, 60°C water bath, pH=3.5, core material 20ml and hot water dilution by in-situ polymerization. The size is around 116 μm. The rough outer surface of microcapsule is composed of agglomerated PMU nanoparticles. The microcapsules basically exhibit good storage stability at room temperature, and they are chemically stable before the heating temperature is up to approximately 200°C.


2015 ◽  
Vol 119 (14) ◽  
pp. 4881-4887 ◽  
Author(s):  
Balachandran Vivek ◽  
Edamana Prasad

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