Self-healable polymer complex with a giant ionic thermoelectric effect.

In this study, we develop a stretchable/self-healable polymer, PEDOT:PAAMPSA:PA, with remarkably high ionic thermoelectric (iTE) properties: an ionic figure-of-merit of 12.3 at 70% relative humidity (RH). The iTE properties of PEDOT:PAAMPSA:PA are optimized by controlling the ion carrier concentration, ion diffusion coefficient, and Eastman entropy, and high stretchability and self-healing ability are achieved based on the dynamic interactions between the components. Moreover, the iTE properties are retained under repeated mechanical stress (30 cycles of self-healing and 50 cycles of stretching). An ionic thermoelectric capacitor (ITEC) device using PEDOT:PAAMPSA:PA achieves a maximum power output and energy density of 4.59 µW‧m-2 and 1.95 mJ‧m-2, respectively, at a load resistance of 10 KΩ, and a 9-pair ITEC module produces a voltage output of 0.37 V‧K-1 with a maximum power output of 0.21 µW‧m-2 and energy density of 0.35 mJ‧m-2 at 80% RH, demonstrating the potential for a self-powering source.

Self-Repairable Silicon Anodes Using a Multifunctional Binder for High-Performance Lithium-Ion Batteries.

Despite of extremely high theoretical capacity of Si (3579 mAh g-1 ), Si anodes suffer from pulverization and delamination of the electrodes induced by large volume change during charge/discharge cycles. To address those issues, herein, self-healable and highly stretchable multifunctional binders, polydioxythiophene:polyacrylic acid:phytic acid (PEDOT:PAA: PA, PDPP) that provide Si anodes with self-healability and excellent structural integrity is designed. By utilizing the self-healing binder, Si anodes self-repair cracks and damages of Si anodes generated during cycling. For the first time, it is demonstrated that Si anodes autonomously self-heal artificially created cracks in electrolytes under practical battery operating conditions. Consequently, this self-healable Si anode can still deliver a reversible capacity of 2312 mAh g-1 after 100 cycles with remarkable initial Coulombic efficiency of 94%, which is superior to other reported Si anodes. Moreover, the self-healing binder possesses enhanced Li-ion diffusivity with additional electronic conductivity, providing excellent rate capability with a capacity of 2084 mAh g-1 at a very high C-rate of 5 C.

Self-Healable and Stretchable Ionic-Liquid-Based Thermoelectric Composites with High Ionic Seebeck Coefficient.

The advancement of wearable electronics, particularly self-powered wearable electronic devices, necessitates the development of efficient energy conversion technologies with flexible mechanical properties. Recently, ionic thermoelectric (TE) materials have attracted great attention because of their enormous thermopower, which can operate capacitors or supercapacitors by harvesting low-grade heat. This study presents self-healable, stretchable, and flexible ionic TE composites comprising an ionic liquid (IL), 1-ethyl-3-methylimidazolium trifluoromethanesulfonate (EMIM:OTf); a polymer matrix, poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP); and a fluoro-surfactant (FS). The self-healability of the IL-based composites originates from dynamic ion-dipole interactions between the IL, the PVDF-HFP, and the FS. The composites demonstrate excellent ionic TE properties with an ionic Seebeck coefficient (Si ) of ≈38.3 mV K-1 and an ionic figure of merit of ZTi  = 2.34 at 90% relative humidity, which are higher than the values reported for other IL-based TE materials. The IL-based ionic TE composites developed in this study can maintain excellent ionic TE properties under harsh conditions, including severe strain (75%) and multiple cutting-healing cycles.

Enhanced Chemical and Electrochemical Stability of Polyaniline-Based Layer-by-Layer Films.

Polyaniline (PANI) has been widely used as an electroactive material in various applications including sensors, electrochromic devices, solar cells, electroluminescence, and electrochemical energy storage, owing to PANI's unique redox properties. However, the chemical and electrochemical stability of PANI-based materials is not sufficiently high to maintain the performance of devices under many practical applications. Herein, we report a route to enhancing the chemical and electrochemical stability of PANI through layer-by-layer (LbL) assembly. PANI was assembled with different types of polyelectrolytes, and a comparative study between three different PANI-based layer-by-layer (LbL) films is presented here. Polyacids of different acidity and molecular structure, i.e., poly(acrylic acid) (PAA), polystyrene sulfonate (PSS), and tannic acid (TA), were used. The effect of polyacids' acidity on film growth, conductivity, and chemical and electrochemical stability of PANI was investigated. The results showed that the film growth of the LbL system depended on the acidic strength of the polyacids. All LbL films exhibited improved chemical and electrochemical stability compared to PANI films. The doping level of PANI was strongly affected by the type of dopants, resulting in different chemical and electrochemical properties; the strongest polyacid (PSS) can provide the highest conductivity and chemical stability of conductive PANI. However, the electrochemical stability of PANI/PAA was found to be better than all the other films.

Highly enhanced electrical properties of lanthanum-silicate-oxide-based SOFC electrolytes with co-doped tin and bismuth in La9.33-x Bi x Si6-y Sn y O26.

Solid oxide fuel cells (SOFCs) are one of the most promising clean energy sources to be developed. However, the operating temperature of SOFCs is currently still very high, ranging between 1073 and 1273 K. Reducing the operating temperature of SOFCs to intermediate temperatures in between 773 and 1073 K without decreasing the conductivity value is a challenging research topic and has received much attention from researchers. The electrolyte is one of the components in SOFCs which has an important role in reducing the operating temperature of the SOFC compared to the other two fuel cell components, namely the anode and cathode. Therefore, an electrolyte that has high conductivity at moderate operating temperature is needed to obtain SOFC with medium operating temperature as well. La9.33Si6O26 (LSO) is a potential electrolyte that has high conductivity at moderate operating temperatures when this material is modified by doping with metal ions. Here, we report a modification of the structure of the LSO by partial substitution of La with Bi3+ ions and Si with Sn4+, which forms La9.33-x Bi x Si6-y Sn y O26 with x = 0.5, 1.0, 1.5, and y = 0.1, 0.3, 0.5, in order to obtain an electrolyte of LSO with high conductivity at moderate operating temperatures. The addition of Bi and Sn as dopants has increased the conductivity of the LSO. Our work indicated highly enhanced electrical properties of La7.83Bi1.5Si5.7Sn0.3O26 at 873 K (1.84 × 10-2 S cm-1) with considerably low activation energy (E a) of 0.80 eV comparing to pristine La9.33Si6O26 (0.08 × 10-2 S cm-1).

A novel hydrothermal synthesis of nanohydroxyapatite from eggshell-calcium-oxide precursors.

Hydroxyapatite (HA) is a material that has been widely applied to replace the damaged bone as a bone implant. Different types of HA have been successfully synthesized by a hydrothermal method based on calcium oxide (CaO) which was originated from chicken eggshells and diammonium hydrogen phosphate (DHP)/(NH4)2HPO4 as their precursors. We present a novel approach to the hydrothermal synthesis of HA form eggshells as a new precursor via a one-step synthesis method. The influence of temperature was also observed to study the effect on the crystallinity, purity, and morphology of obtained HAs. The synthesis was carried out at two different temperatures, 200 °C (HA-200) and 230 °C (HA-230) for 48 h respectively. The structures, purities, and morphologies of hydroxyapatite were analyzed by X-ray Diffraction (XRD), Fourier Transform Infra-Red (FTIR), and Scanning Electron Microscopy- Energy Dispersive Spectroscopy (SEM-EDS), and Transmission electron microscopy (TEM). The XRD patterns show the HA main phase indicated the purity of 96.5% for HA-200 and 99.5% for HA-230. The TEM micrograph suggested a hexagonal-like of HA with an average particle size of 92.61 nm. Hexagonal-like of HAs are suitable for bone implants and further application.

Maleic anhydride grafted onto high density polyethylene with an enhanced grafting degree via monomer microencapsulation.

High-density polyethylene (HDPE) is among the flexible polymers on account of its appropriate processability and adequate mechanical properties. Grafting reactive monomers such as glycidyl methacrylate (GMA) and maleic anhydride (MAH) onto polyethylene was one of the ultimate choices to improve the physicochemical properties of HDPE. MAH is an appropriate option for grafting onto HDPE owing to its low reactivity and it relatively undergoes a direct grafting onto the polymer. The grafting of MAH on HDPE copolymerization has been conducted using monomer microencapsulation method in this study. The monomer microencapsulation samples were extracted stratified using acetone and xylen. Samples were then analyzed using titration, melt flow rate, FTIR, DSC, TGA and C-NMR. The results showed the degree of paste monomer on HDPE with a microencapsulation method was greater when compared to the usual method. We were successfully improving the grafting degree of MAH onto HDPE by using a simple blending method. The pre-microencapsulated HDPE provided an increasing in grafting degree of 1.88% (HDPE-g-MAH) over the conventional one which shows the value of 1.39% (HDPE-g-MAH).

Synthesis and characterization of sulfonated poly(vinylidene fluoride-co-hexafluoropropylene)/sAl2O3 composites as a novel-alternative electrolyte membranes of Nafion.

Fuel cell membrane of Nafion is commonly used as the electrolyte material of fuel cell which has good mechanical properties, but the hydrophobicity reduce its proton conductivity. Thus, the other polymer is used for the electrolyte membrane. A polymer modification of sulfonated poly (vinylidene fluoride-co-hexafluoropropylene) (PVDF-co-HFP) by attaching sulfonate group and oxide compounds such as sAl2O3 would enhance the proton conductivity. The research is aimed to modify PVDF-co-HFP via the addition of sAl2O3 or pristine Al2O3 and studying the effect of sulfonated Al2O3 on the conductivity. The research includes Al2O3 particles synthesis, the sulfonation of Al2O3, the membrane preparation, the sulfonation of membrane, and the characterisation of membrane using FTIR, SEM-EDX, and Four-point Probe Electrical Device Analysis. SEM-EDX analysis explained that the 6% addition of Al2O3 showed denser cross-sectioned membrane rather than the 9% addition of Al2O3. The highest conductivity achieved can be revealed at the 6% sAl2O3 addition on PVDF-co-HFP membrane as 2.27 × 10-3 S cm-1 which is higher than a previous study.