CuxNi1-xO nanostructures and their nanocomposites with reduced graphene oxide: Synthesis,characterization, and photocatalytic applications

NiO nanostructure was synthesized using a simple co-precipitation method and was embedded on reduced graphene oxide surface via ultrasonication. Structural investigations were made through X-ray diffraction (XRD) and functional groups were confirmed by Fourier transform infrared spectroscopy (FTIR). XRD analysis revealed the grain size reduction with doping. Fourier transform infrared spectroscopy confirmed the presence of metal-oxygen bond in pristine and doped NiO nanostructure as well as the presence of carbon containing groups. Scanning electron microscopy (SEM) indicated that the particle size decreased when NiO nanostructure was doped with copper. BET surface area was found to increase almost up to 43 m²/g for Cu doped NiO nanostructure/rGO composite. Current-voltage measurements were performed using two probe method. UV–Visible spectroscopic profiles showed the blue and red shift for Cu doped NiO nanostructure and Cu doped NiO Nanostructure/rGO composite respectively. Rate constant for Cu doped NiO nanostructure/rGO composite found to increase 4.4 times than pristine NiO nanostructure.     

Nanoraspberry-like palladium/spongy nickel oxide for electrooxidation of five light fuels

The spongy nickel oxide (SNO) was synthesized the solution combustion method. The SNO was selected as a promoter to boost the catalytic activity of nanoraspberry-like palladium (NRPd) toward electrooxidation of five light fuels (LFs): methanol, ethanol, formaldehyde, formic acid, and ethylene glycol. The X-ray powder diffraction, Fourier-transform infrared spectroscopy (FT-IR), scanning electron microscopy, and field emission scanning electron microscope techniques were used for the materials characterization. In comparison with nonpromoted Pd, the NRPd-SNO electrocatalyst shown an excellent efficiency in parameters like the electrochemical active surface area and anti-CO poisoning behavior. The turnover data and the parameters, including reaction order, activation energy, and the coefficients of electron transfer and diffusion, were evaluated for the each process of LFs electrooxidation. The outcome for NRPd-SNO activity toward LFs electrooxidation was compared to some reported electrodes. The SNO increases the removal of intermediates created in the oxidation of LFs that can poison the surface of palladium catalyst. This is due to the presence of the lattice oxygens in SNO structure and Ni switching between its high and low valances. The compatibility of the adsorption process of LFs on the surface of the NRPd-SNO catalyst with different isotherms was determined by studying the Tafel polarization and calculating the surface coverage.     

Catalytic combustion of methane over a highly active and stable NiO/CeO2 catalyst

In the last decades, many reports dealing with technology for the catalytic combustion of methane (CH₄) have been published. Recently, attention has increasingly focused on the synthesis and catalytic activity of nickel oxides. In this paper, a NiO/CeO₂ catalyst with high catalytic performance in methane combustion was synthesized via a facile impregnation method, and its catalytic activity, stability, and water-resistance during CH₄ combustion were investigated. X-ray diffraction, low-temperature N₂ adsorption, thermogravimetric analysis, Fourier transform infrared spectroscopy, hydrogen temperature programmed reduction, methane temperature programmed surface reaction, Raman spectroscopy, electron paramagnetic resonance, and transmission electron microscope characterization of the catalyst were conducted to determine the origin of its high catalytic activity and stability in detail. The incorporation of NiO was found to enhance the concentration of oxygen vacancies, as well as the activity and amount of surface oxygen. As a result, the mobility of bulk oxygen in CeO₂ was increased. The presence of CeO₂ prevented the aggregation of NiO, enhanced reduction by NiO, and provided more oxygen species for the combustion of CH₄. The results of a kinetics study indicated that the reaction order was about 1.07 for CH₄ and about 0.10 for O₂ over the NiO/CeO₂ catalyst.     

Dielectric properties and electromagnetic interference shielding studies of nickel oxide and tungsten oxide reinforced polyvinylchloride nanocomposites

ABSTRACT

Polyvinylchloride (PVC)/nickel oxide (NiO)/tungsten oxide (WO₃) nanocomposite films were prepared via solution casting technique. The crystallinity, morphology, and the analysis of dispersion state of PVC/NiO/WO₃ nanocomposite was carried out using X-ray diffraction (XRD) and scanning electron microscopy (SEM). The dielectric studies of nanocomposite films were investigated and a maximum dielectric constant of 2.3 with dielectric loss (tan δ) of 2.4 was attained. The EMI shielding studies were carried out in the X and Ku-band frequency range (8 GHz-18 GHz). The maximum SE of 15.78 dB in X-band and 12.05 dB in Ku-band was achieved for 75/20/5 compositions of the PVC/NiO/WO₃ nanocomposite.     

Room temperature ferromagnetic ordering of NiO films through exchange coupling

NiO films were deposited by sputtering with a relatively high oxygen partial pressure, followed by subsequent annealing in air. The as-deposited film is amorphous. The amorphous film gradually turns to crystalline structure with the increase in annealing temperature. The film annealed at 673 K shows strong ferromagnetism at room temperature, whereas, there is no room-temperature ferromagnetic ordering for the as-deposited amorphous NiO film or the film after annealed at 873 K. The ferromagnetism is due to the finite size effect and the high Curie temperature above room temperature is associated with the interaction between ferromagnetic NiO crystalline nanoclusters and antiferromagnetic amorphous matrix.     

Synthesis and Humidity Sensing Properties of NiO Intercalated Polyaniline Nanocomposite

The exercising cooperative and interfacial properties of metal oxide and conducting polymer as a sensing material for humidity detection was the focal point of this study. In this piece of work nano sized NiO and its composite with polyaniline has been prepared. The cooperative effects of NiO on stuructural, morphology, humidity sensing behaviour of PANI has been investigated. Prepared materials were characterized by infrared spectroscopy (FT-IR), X-ray diffraction (XRD), scanning electron microscope (SEM),UV–VIS spectroscopy and Four probe techniques. The result reveals that the NiO strongly influences on polymer chain, crystallinity, stability, electrical and optical properties of PANI, which improves its viability in technology development. Finally, PANI/NiO was used for electrochemical humidity sensing of a closed atmosphere. The result reveals that 100 times increase in sensitivity of PANI due to the presence of NiO nano particles. Finally, the results indicate that the impact of NiO on PANI makes it promising perspective materials for humidity monitoring of closed chamber with improved sensing parameters over several method and materials.     

Multispectral photodetection using low-cost sputtered NiO/Ag/ITO heterostructure: From design concept to elaboration

High-performance multispectral photodetectors (PDs) are highly attractive for the emerging optoelectronic applications. In this work, a new broadband PD based on p-NiO/Ag/n-ITO heterostructure was fabricated by RF magnetron sputtering technique at room temperature. The tri-layered structure offering multispectral detection property was first identified using theoretical calculations based on combined FDTD and Particle Swarm Optimization (PSO) techniques. The crystal structure of the elaborated sensor was analyzed using X-ray diffraction (XRD) method. The device optical properties were investigated by UV–Vis–NIR spectroscopy. The NiO/Ag/ITO heterostructured PD shows a high average absorbance of 63% over a wide spectrum range of [200 nm–1100nm]. Compared with NiO and ITO thin-films, the performances of the heterostructured device are considerably enhanced. It was found that the prepared PD with NiO/Ag/ITO heterostructure merges the benefits of multispectral photodetection with reduced optical losses and efficient transfer of photo-induced carrier. The device demonstrated a high I_ON/I_OFF ratio of 78 dB and an enhanced responsivity under UV, visible and NIR lights (171 mA/W at 365 nm, 67 mA/W at 550 nm and 93 mA/W at 850 nm). The broadband photodetection property enabled by the optimized NiO/Ag/ITO heterostructure opens a new route for the elaboration of low-cost devices that can offer multiple sensing purposes, which are highly suitable for optoelectronic applications.     

Enhancing the flash-sinterability of BaZr0.1Ce0.7Y0.2O3-δ proton-conducting electrolyte by nickel oxide doping for possible application in SOFCs

In the present work, effects of nickel oxide doping on flash-sinterability of BaZr_0.1Ce_0.7Y_0.2O_3-δ compound were investigated. A single-phase BZCY7 powder was synthesized by the solid-state reaction route. The effects of using 0.5, 1, 1.5, and 2 wt% of NiO additive on flash sintering of BZCY7 samples were examined. It was revealed that using 0.5 wt% of NiO additive can reduce the onset temperature of flash sintering in all the applied electric fields in the range of 100–500 V/cm and significantly enhances the sinterability of the BZCY7 compound. Microstructural investigations, using field emission scanning electron microscopy and energy-dispersive X-ray mapping, showed that NiO doping can lead to larger grain sizes, while no detectable segregation or second phase was observed. Utilizing electrochemical impedance spectroscopy, the total conductivity of samples at 600 and 700 °C was measured as 4.4 × 10^?3 and 7.0 × 10^?3 S/cm for the undoped BZCY7, and 8.6 × 10^?3 and 1.4 × 10^?2 S/cm for the 0.5 wt% NiO doped BZCY7 sample, respectively. The activation energies of conduction were determined as 0.37 and 0.41 eV for the doped and undoped samples, which represent the presence of predominant and facile protonic conduction.     

Role of oxygen vacancies on the energy storage performance of battery-type NiO electrodes

In this study, the influence of the surface oxygen vacancies on the energy storage performance of electrodes based on nickel oxide (NiO) nanoparticles was investigated. NiO samples were synthesized by three facile and low-cost syntheses routes: nitrate calcination, citrate, and combustion methods. The concentration of surface defects in NiO powders was determined using XPS analyses, which showed a higher amount of oxygen vacancies for the sample obtained by nitrate calcination. According to the cyclic voltammetry (CV) and galvanostatic charge-discharge (GCD) curves, NiO-based electrodes were classified as battery-like. CV results suggest that redox reactions are diffusion-controlled processes with a faster diffusion rate for the sample obtained by the nitrate calcination method. This is in accordance with the GCD and electrochemical impedance spectroscopy (EIS) results, with higher specific capacity and higher electrical conductivity (lower equivalent series resistance) for the sample obtained by nitrate calcination. The results indicate that oxygen vacancies play an important role in the electrochemical performance of battery-type NiO electrodes.     

Ni/La2O3 catalysts for dry reforming of methane: Effect of La2O3 synthesis conditions on the structural properties and catalytic performances

10 wt%Ni/La₂O₃ catalysts for dry reforming of methane (DRM) were synthesized by wetness impregnation of lanthana supports prepared using sol-gel citric method with and without NH₃ addition (Ni–La CA-NH₃ and Ni–La CA, respectively). The support preparation conditions affect the nature, phase composition, and distribution of Ni phases (LaNiO₃, NiO and La₃Ni₂O₆). The gradient temperature DRM tests (400–800 °C) reveal higher catalytic activity of Ni–La CA (at 650 °C, X(CO₂) = 65.7%, X(CH₄) = 54.6%, H₂/CO = 0.71). The Ni–La CA-NH₃ shows higher stability (at 650 °C and 24 h, X(CO₂): 73.7% => 76.4%, X(CH₄): 64.7% => 64.6%, H₂/CO: 0.77 => 0.72). For both catalysts, La₂O₂CO₃ phase is formed after long run tests at 650 °C 24 h, with the greater TGA weight loss and stronger deactivation being observed for Ni–La CA. The H₂-reduced Ni La CA-NH₃ features ultrasmall (1–2 nm) Ni NPs strongly interacting with the support. Catalyst nature affects the amount of carbon coke formed.