Graphene/TiO<Subscript>2</Subscript> hydrogel: a potential catalyst to hydrogen evolution reaction

In this study, graphene was synthesized from graphite. Graphite was oxidized via modified Hummer’s method and sonicated to form graphene oxide (GO). Infrared spectroscopy revealed the successful oxidation of graphite by the emergence of oxygen functionalities. The spectrum of GO showed peaks at 3270, 1629, 1227 and 1096 cm^?1, indicating O–H, C=O, C–OH and C–O–C functional groups, respectively. Graphene hydrogels were prepared by the addition of L-ascorbic acid to GO suspensions and subsequent heating at 90^°C. Composite hydrogels of graphene and titanium (IV) oxide (TiO₂) were synthesized with various TiO₂ to GO mass ratios. Composites were applied to photocatalytic hydrogen evolution reaction (HER) and the hydrogen gas produced was analysed by gas chromatography with thermal conductivity detector. Highest HER yield was 66.00% H₂.     

Effect of ‘Al’ concentration on spin-dependent resonant tunnelling in InAs/Ga<Subscript>1−<Emphasis Type="Italic">y</Emphasis></Subscript>Al<Subscript><Emphasis Type="Italic">y</Emphasis></Subscript>As symmetrical double-barrier heterostructures

The effect of ‘Al’ concentration on spin-dependent tunnelling in strained non-magnetic symmetric double-barrier semiconductor has been theoretically investigated. The separation between spin-up and spin-down components, barrier transparency, polarization efficiency and tunnelling lifetime were calculated using the transfer matrix approach. The separation between spin-up and spin-down resonances and tunnelling lifetime were reported for the first time in the case of InAs/Ga_1?y Al _y As heterostructures for various ‘Al’ concentrations and for various barrier widths. Cent percentage polarization can be obtained in this strained non-magnetic double-barrier semiconductor even without any external field.     

Luminescence properties of terbium-doped Li<Subscript>3</Subscript>PO<Subscript>4</Subscript> phosphor for radiation dosimetry

A polycrystalline sample of Li₃PO₄:Tb³⁺ phosphor was successfully synthesized using solid-state diffusion method. This synthesis method is of low cost, low temperature and does not require any other atmospheres for the synthesis. The powder X-ray diffraction (PXRD), photoluminescence (PL) emission and excitation spectra, thermoluminescence (TL) and optically stimulated luminescence (OSL) were measured. The particle size was calculated using the Debye Scherrer formula and found to be 79.42 nm. PL emission spectra of Li₃PO₄:Tb³⁺ phosphor show the strong prominent peak at 544 nm corresponding to ⁵D₄ to ⁷F₅ transitions of Tb³⁺. The OSL sensitivity of prepared Li₃PO₄:Tb³⁺ phosphor was 50% of that of α-Al₂O₃:C. Its decay curve consists of three components with photoionization cross-sections 0.44 × 10^?17, 3.09 × 10^?17 and 23×10^?17 cm². The TL glow curve of the prepared sample consists of two characteristic peaks, which were deconvoluted using the peak fit software, and kinetic parameters were determined using the peak shape method. TL intensity was compared with that of the commercially available TLD-500 phosphor. OSL dose response was linear in the measured range and the minimum detectable dose (MDD) was found to be 67.42 μGy, while fading of the OSL signal was found to be about 27% in 4200 min after which the OSL signal stabilizes.     

Synthesis,characterisation and non-isothermal degradation kinetics of novel poly(mono ethylene glycol dimethacrylate-co-4-aminobenzoate)

Synthesis of a novel co-polymer made by the addition polymerisation between MEGDMA and 4-AB by aza-Michael addition (AMA) polymerisation method is a fascinating field of research. The present investigation yielded a hazardous metal catalyst-free and toxic solvent-free methodology. The AMA polymerisation was carried out at five different [ M ₁/M ₂] values under N₂ atmosphere at 100^°C for 2 h. Thus, obtained co-polymer was characterized by Fourier transform infrared spectroscopy, UV–visible reflectance spectroscopy, X-ray diffraction, differential scanning calorimetry, thermogravimetric analysis and scanning electron microscopy (SEM). The SEM image confirmed the formation of polymer nanoparticles. The non-isothermal degradation kinetics was followed with four different models, such as Flynn-Wall-Ozawa, Auggis-Bennet, Kissinger and Friedman method. Among the models used, the Kissinger method yielded the lowest degradation kinetics. The degradation kinetics of the co-polymer was followed with the help of model-free methods. Moreover, it was critically compared with the literature.     

Effect of temperature on the characteristics of ZnO nanoparticles produced by laser ablation in water

Effect of the water temperature on the characteristics of zinc oxide nanoparticles (NPs) produced by laser ablation process is investigated experimentally. The fundamental wavelength of a Q-switched Nd:YAG laser was employed to irradiate a high-purity zinc plate in distilled water at different temperatures of 0, 20, 40 and 60^°C. The produced NPs were diagnosed by UV–vis–NIR spectroscopy, X-ray diffraction method, transmission electron microscopy and scanning electron microscopy. Results show that with increase in the water temperature from 20 to 60^°C, size of NPs decreases while their bandgap energy increases. Maximum ablation rate occurs at the highest temperature. Crystalinity also increases with increase in the water temperature. The abnormal behaviour of water at 0–4^°C affects the NPs characteristics.     

Selective extraction and detection of noble metal based on ionic liquid immobilized silica gel surface using ICP-OES

In this study, an efficiently employed ionic liquid combined with commercially available silica gel (SG–ClPrNTf₂) was developed for selective detection of gold(III) by use of inductively coupled plasma–optical emission spectrometry (ICP-OES). The selectivity of SG–ClPrNTf₂ was evaluated towards seven metal ions, including Y(III), Mn(II), Zr(IV), Pb(II), Mg(II), Pd(II) and Au(III). Based on pH study and distribution coefficient values, the SG–ClPrNTf₂ phase was found to be the most selective towards Au(III) at pH 2 as compared to other metal ions. The adsorption isotherm of Au(III) on the SG–ClPrNTf₂ phase followed the Langmuir model with adsorption capacity of 59.48 mg g^?1, which was highly in agreement with experimental data of adsorption isotherm study. The kinetics study indicated that Au(III) adsorption kinetics data were well fit with the pseudo-second-order kinetic model on the basis of correlation coefficient fitting (0.996) and adsorption capacity agreement (62.26 mg g^?1). Furthermore, SG–ClPrNTf₂ phase was effectively performed for the determination of Au(III) in real water samples with satisfactory results.     

Structural and frequency dependencies of a.c. and dielectric characterizations of epitaxial InSb-based heterojunctions

In this work, heterojunction of InSb/InP was grown by liquid phase epitaxy (LPE). Surface morphology and crystalline structure of the heterojunction were characterized by scanning electron microscopy (SEM) and X-ray diffraction (XRD). The frequency and temperature dependences of a.c. conductivity and dielectric properties of the heterojunctions were investigated in the ranges of 100 kHz–5 MHz and 298–628 K, respectively. The a.c. conductivity and its frequency exponents were interpreted in terms of correlated barrier hopping model (CBH), as the dominant conduction mechanism for charge carrier transport. The calculated activation energy, from the Arrhenius plot, was found to decrease with increasing frequency. Experimental results of both dielectric constant ε ₁ and dielectric loss ε ₂ showed a remarkable dependence of both frequency and temperature.     

Preparation and characterization of PAN–KI complexed gel polymer electrolytes for solid-state battery applications

The free standing and dimensionally stable gel polymer electrolyte films of polyacrylonitrile (PAN): potassium iodide (KI) of different compositions, using ethylene carbonate as a plasticizer and dimethyl formamide as solvent, are prepared by adopting ‘solution casting technique’ and these films are examined for their conductivities. The structural, miscibility and the chemical rapport between PAN and KI are investigated using X-ray diffraction, Fourier transform infrared spectroscopy and differential scanning calorimetry methods. The conductivity is enhanced with the increase in KI concentration and temperature. The maximum conductivity at 30°C is found to be 2.089 × 10^?5 S cm^?1 for PAN:KI (70:30) wt%, which is nine orders greater than that of pure PAN (< 10^?14 S cm^?1). The conductivity-temperature dependence of these polymer electrolyte films obeys Arrhenius behaviour with activation energy ranging from 0.358 to 0.478 eV. The conducting carriers of charge transport in these polymer electrolyte films are identified by Wagner’s polarization technique and it is found that the charge transport is predominantly due to ions. The better conducting sample is used to fabricate the battery with configuration K/PAN + KI/I₂+ C + electrolyte and good discharge characteristics of battery are observed.     

Reinforcing graphene oxide/cement composite with NH<Subscript>2</Subscript> functionalizing group

In this study, pure and NH₂-functionalized graphene oxide (GO) nanosheets have been added to the cement mortar with different weight percents (0.05, 0.10, 0.15, 0.20 and 0.25 wt%). In addition, the effects of functionalizing GO on the microstructure and mechanical properties (flexural/compressive strengths) of cement composite have been investigated for the first time. Scanning electron microscopy (SEM) images showed that GO filled the pores and well dispersed in concrete matrix, whereas exceeding GO additive from 0.10 wt% caused the formation of agglomerates and microcracks. In addition, mercury intrusion porosimetry confirmed the significant effects of GO and functionalizing groups on filling the pores. NH₂-functionalizing helped to improve the cohesion between GO nanosheets and cement composite. Compressive strengths increased from 39 MPa for the sample without GO to 54.23 MPa for the cement composites containing 0.10 wt% of NH₂-functionalized GO. Moreover, the flexural strength increased to 23.4 and 38.4% by compositing the cement paste with 0.10 wt% of pure and NH₂-functionalized GO, compared to the sample without GO, respectively. It was shown that functionalizing considerably enhanced the mechanical properties of GO/cement composite due to the interfacial strength between calcium silicate hydrates (C-S-H) gel and functionalized GO nanosheets as observed in SEM images. The morphological results were in good agreement with the trend obtained in mechanical properties of GO/cement composites.     

Synthesis,structural and optical properties of nanoparticles (Al,V) co-doped zinc oxide

The synthesis by the sol–gel method, structural and optical properties of ZnO, Zn_0.99Al_0.01O (AlZ), Zn_0.9V_0.1O (VZ) and Zn_0.89Al_0.01V_0.1O (AlVZ) nanoparticles was reported. The approach was slow release of water for hydrolysis by esterification reaction followed by a supercritical drying in ethyl alcohol. After thermal treatment at 500^°C in air, the obtained nanopowders were characterized by various techniques such as transmission electron microscopy, X-ray diffraction and photoluminescence (PL) spectroscopy. The structural properties showed that the ZnO nanoparticles with an average particle size of 25 nm exhibit hexagonal wurtzite structure. From the optical studies, it was found that the optical band gap was located between 2.97 and 3.17 eV. The obtained electrical properties showed the potential application of the samples in optoelectronic devices. The powder of AlVZ presented a strong luminescence band in the visible range. The PL band energy position presented a small blue shift with the increase of measurement temperature. Different possible attributions of this emission band will be discussed.