Effect Of Ni Doping Research Articles

Ni-modified BaTiO3 film prepared by sol-gel with high energy storage performance

The development of lead-free dielectric capacitors with high recoverable energy storage density and high energy storage efficiency is important for improving the overall performance of electronic and power systems. BaTiO3 (BTO) is one of the most common ferroelectric materials and has attracted much attention for energy storage applications in the past decades due to its excellent dielectric and ferroelectric properties. However, high remnant polarization and low electrical breakdown strength of BTO limit its development in energy storage applications. Many efforts (e.g., elements doping, interface/heterostructure, etc.) have been made to improve the energy storage density of BTO thin films. In this paper, Ba1-xNixTiO3 thin films (x = 0, 0.02, 0.04, 0.06, 0.08; abbreviated as BNxT) were synthesized via sol-gel and spin-coated method. The effect of Ni doping on the structural, dielectric, ferroelectric and energy storage properties of BTO thin films has been studied. The results confirmed that with the increase of Ni doping, a second phase arises and the dielectric constant decreases. While appropriate Ni doping led to the improvement of the breakdown strength, further increase of Ni deteriorated the energy storage because of the high oxygen vacancy. Finally, optimized energy storage performance was obtained for BN0.04T thin film: dielectric constant of 401, dielectric loss of 0.002, recoverable energy density of 20.2 J/cm3 and energy storage efficiency of 83.6% at 965 kV/cm. Meanwhile, the remnant and maximum polarization of the films were 0.06 μC/cm2 and 50 μC/cm2, respectively. BN0.04T thin film has an excellent application prospect and is expected to appear as a component in the future composite energy storage film system.

Enhancing Low-Temperature Sensor Applications: Synergistic Effects of Ni Doping and SnO2 Interlayer on Spin-Coated ZnO Thin Films on Glass Substrate

This study investigates the effects of Nickel doping and a SnO2 interlayer on the structural, morphological, optical, and electrical properties of ZnO thin films. Undoped and Ni-doped ZnO films were fabricated on glass substrates, with and without an SnO2 interlayer, using the sol-gel spin coating method. The samples—denoted as ZG (undoped ZnO), NZG (Ni-doped ZnO), ZSG (undoped ZnO with SnO2 interlayer), and NZSG (Ni-doped ZnO with SnO2 interlayer)—underwent comprehensive characterization via XRD, AFM, PL, UV-Vis spectroscopy, Hall effect measurements, Hot probe, and Two-point method. XRD analysis confirmed successful Ni incorporation and enhanced ZnO crystallinity, particularly in the presence of the SnO2 interlayer. AFM analysis revealed improved grain distribution and size due to the synergistic effects of Ni doping and the SnO2 interlayer. UV-Vis results indicated significant impacts on transparency and the Urbach energy, with Ni doping alone broadening the bandgap. PL measurements showed that the synergistic effects quenched UV luminescence associated with the glass substrate, enhancing visible luminescence. Chromaticity analysis suggested that ZSG and NZSG samples are suitable for warm blue region applications. Electrical measurements revealed n-type conductivity across all films except NZG, with Ni doping increasing resistivity. Additionally, the ZSG (PTC) sensor exhibited a slightly higher sensitivity (0.3852 Ω/°C) compared to the NZSG sensor (0.3782 Ω/°C), with a similar trend observed in NTC sensors. These findings suggest that Ni-doped ZnO films with SnO2 interlayers could potentially serve as thermistors and RTDs, offering promising applications in temperature sensing and optoelectronics.

Effects of Ni-Doping in CuMn2O4 Spinel Coatings for Interconnects in Solid Oxide Fuel Cells

Effects of Ni-Doping in CuMn2O4 Spinel Coatings for Interconnects in Solid Oxide Fuel Cells

Exploring electrochemical kinetic behaviors and interfacial charge transfer of pure and Ni-doped ZnFe2O4 nanoparticles-based sensing nanoplatform for ultra-sensitive detection of chloramphenicol

ZnFe2O4 (ZFO) nanomaterial was doped with a divalent transition metal cation of Ni2+ (NixZn1-xFe2O4, x=0, 0.2, 0.4, and 0.8) and characterized by various analytical techniques. Powder X-ray diffraction revealed the formation of a single-phase cubic spinel structure, while the stabilization of crystal structure for Ni2+-doped samples was observed. The average crystalline size, d-spacing, and lattice parameters increased with increasing in Ni2+ concentration within NixZn1-xFe2O4, due to differences in the ionic radius, the cation distribution at A-B sites, and the creation of surface oxygen vacancies within ZFO structure. From electrochemical measurements, NixZn1-xFe2O4-based electrodes showed excellent enhancements in charge transfer ability and conductivity with the highest rate constant (0.018 ms−1), the lowest peak-to-peak separation (206 mV), the lowest Rct (118 Ω), and the largest electrochemical active area (0.248 cm2), compared to that of bare SPE. Among them, Ni0.8Zn0.2Fe2O4/SPE provided outstanding electrochemical behaviors and achieved the best sensing performance with the widened concentration linear range from 0.25 to 50 μM and a rather low detection limit of 0.2 μM for chloramphenicol detection. The most important reason for this positive advance comes from the unique synergistic effects of Ni doping into the ZFO host structure. The excellent enhancements in adsorption capacity (Г) (1.4 times higher), number of oxygen vacancies, charge transfer rate constant (approximately 1.15 times higher), and catalytic rate constant (30 times greater) were recorded at Ni-doped ZFO-based electrodes, compared to pure ZFO-based electrode. Furthermore, the detailed hypotheses and possible mechanisms explaining these impressive enhancements were explored. Our work provides insight into the correlation between the Ni-doping and electrochemical characteristics, which has implications for tailoring the electrochemical performance of spinel ferrites across diverse applications and the design of novel spinel ferrite nanomaterials.

Effect of Ni doping on the magnetic and photocatalytic properties of CoFe2O4 nanoparticles

Effect of Ni doping on the magnetic and photocatalytic properties of CoFe2O4 nanoparticles

Preparation and sodium storage properties of Ni-CoFe2O4/Reduced graphene oxide

The Ni-doped CoFe2O4 graphene composites (Ni-CFO/RGO) have been successfully prepared using the microwave-assisted method. The substance is a novel nanocomposite structure in which CoFe2O4 nanoparticles are tightly and uniformly attached to graphene hybrid nanosheets. The synergistic effect of Ni doping and CoFe2O4 can reduce the volume expansion of CoFe2O4 in the reaction process and inhibit the stacking of graphene. Because the Ni-CFO/RGO composite is structurally stable during the electrochemical reaction, it has a good theoretical capacity. Excellent carbon composite can further enhance the electron transport performance and structural stability of the material, thereby improving the electrochemical performance and cycle life of the material. Doping Ni2+ into metal oxides can not only form oxygen vacancies, and improve the transport capacity of sodium ions, but also broaden the electron transport channel. In addition, the catalyst can form a composite structure with metal oxide, which can effectively inhibit its volume expansion. At the same time, reacting with carbon materials, can also effectively reduce the accumulation of carbon, thereby reducing its resistance. After 200 cycles at a current density of 0.05 A g−1, it can provide a high sodium storage capacity of 380.6 mAh g−1, which still keeps 203.4 mAh g−1 at 1.5 A g−1.

Impact of Nickel doping on microstructure and impedance spectroscopy of multiferroic YCrO3

In this work, we study the effect of Ni-doping on the structural and impedance spectroscopy properties of the polycrystalline YCrO3 ceramic sample. The structural analysis shows all the samples crystallize in an orthorhombic structure with the Pnma space group. The depressed and asymmetric semicircle of complex impedance spectra indicates that the relaxation of charge carriers is of non-Debye type, where the thermally activated charge carriers control it. The temperature dependence of relaxation time and electrical conductivity exhibit an anomaly in the vicinity of diffuse-like relaxor transition temperature (TC ∼ 460 K). The analysis of conductivity data shows hopping-type charge conduction. The analysis further indicates that while the dc conductivity increases continuously, the activation energy shows a non-monotonous variation with Ni concentration.

Effect of Ni doping on the microstructure and electrical properties of Ba–Co–O NTC ceramics

Effect of Ni doping on the microstructure and electrical properties of Ba–Co–O NTC ceramics

Synergistic effect of Ni doping on the dielectric and electrochemical properties of WO3 nanostructures for supercapacitor applications

Synergistic effect of Ni doping on the dielectric and electrochemical properties of WO3 nanostructures for supercapacitor applications

High Capacity and Fast Kinetics Enabled by Metal-Doping in Prussian Blue Analogue Cathodes for Sodium-Ion Batteries.

Prussian blue analogues (PBAs) have gained tremendous attention as promising low-cost electrochemically-tunable electrode materials, which can accommodate large Na+ ions with attractive specific capacity and charge-discharge kinetics. However, poor cycling stability caused by lattice strain and volume change remains to be improved. Herein, metal-doping strategy has been demonstrated in FeNiHCF, Na1.40Fe0.90Ni0.10[Fe(CN)6]0.85 ⋅ 1.3H2O, delivering a capacity as high as 148 mAh g-1 at 10 mA g-1. At an exceptionally high rate of 25.6 A g-1, a reversible capacity of ~55 mAh g-1 still can be obtained with a very small capacity decay rate of 0.02 % per cycle for 1000 cycles, considered one of the best among all metal-doped PBAs. This exhibits the stabilizing effect of Ni doping which enhances structural stability and long-term cyclability. In situ synchrotron X-ray diffraction reveals an extremely small (~1 %) change in unit cell parameters. The Ni substitution is found to increase the electronic conductivity and redox activity, especially at the low-spin (LS) Fe center due to inductive effect. This larger capacity contribution from LS Fe2+C6/Fe3+C6 redox couple is responsible for stable high-rate capability of FeNiHCF. The insight gained in this work may pave the way for the design of other high-performance electrode materials for sustainable sodium-ion batteries.

Effect of Ni-doping on the structural and electronic properties of metal halide perovskite CsSnBr3: a DFT study

The structural and electronic properties of pure and Ni-doped perovskite CsSnBr3 in unit cell and supercell were computed using density functional theory at ambient pressure. Computed formation energy values of undoped and Ni-doped CsSnBr3 compounds show that these structures are stable. We used both standard DFT and HSE06 calculation in electronic band structure of pure and Ni-doped CsSnBr3 compounds. Since the band gap of undoped and Ni-doped CsSnBr3 compounds is located at the R symmetry point in the Brilloun zone, these compounds are materials with a direct band gap. In the HSE06 calculation, it was found that the band gap of 12.5% Ni doped-CsSnBr3 increased significantly from 1.1162 eV to 1.4343 eV. The electron charge density, Bader charge analysis and density of states reveal a strong covalent bond between Sn-Br (Ni-Br) and a strong ionic bond between Cs-Br. The direct electronic band gaps of undoped and Ni-doped CsSnBr3 perovskites in the visible energy range show that these compounds can be used effectively in optical applications.

Cobalt telluride regulated by nickel for efficient electrooxidation of 5-hydroxymethylfurfural

Replacing the anodic oxygen evolution reaction (OER) in water splitting with 5-hydroxymethylfurfural oxidation reaction (HMFOR) can not only reduce the energy required for hydrogen production but also yield the valuable chemical 2,5-furandicarboxylic acid (FDCA). Co-based catalysts are known to be efficient for HMFOR, with high-valent Co being recognized as the main active component. However, efficiently promoting the oxidation of Co2+ to produce high-valent reactive species remains a challenge. In this study, Ni-doped CoTe (CoNiTe) nanorods were prepared as efficient catalysts for HMFOR, achieving a high HMFOR current density of 65.3 mA cm−2 at 1.50 V. Even after undergoing five successive electrolysis processes, the Faradaic efficiency (FE) remained at approximately 90.7 %, showing robust electrochemical durability. Mechanistic studies indicated that Ni doping changes the electronic configuration of Co, enhancing its charge transfer rate and facilitating the oxidation of Co2+ to high-valent CoO2 species. This work reveals the effect of Ni doping on the reconfiguration of the active phase during HMFOR.

Insights into the effect of Ni doping on In2S3 for enhanced activity and selectivity of photocatalytic CO2 reduction

The limited photocatalytic CO2 reduction performance mainly lies in the low utilization of photogenerated electrons during the reaction. In this work, we developed the defect level within the Ni-doped In2S3 nanotube photocatalysts via a simple solvothermal method to increase the available amount of photogenerated electrons for enhanced photocatalytic CO2 reduction performance than the pristine In2S3. The introduction of Ni element into the lattice of In2S3 could significantly improve the photocatalytic activity and selectivity without destruction of the nanotube structure of In2S3. The yield of CO reaches 243.2 μmol/g/h under visible light, which is the highest reported value among In2S3 photocatalysts, and is 8.2 times more than the pure In2S3. Moreover, by modulating the doping amount of Ni element, the selectivity of CO varied from 27.7% to 51.0%. Further characterizations suggest that the doping of Ni element altered the electronic bandgap arrangement of In2S3, where the position of the conduction band is conducive to the activation of CO2 molecules. Moreover, the defect level resulting from Ni-doping not only facilitates the separation of photoexcited electron-hole pairs but also suppresses the recombination of electrons and holes. This study provides an available and reliable strategy for enhancing the photocatalytic CO2 reduction performance of related sulfide photocatalytic materials in future studies.

Study the Effect of Ni Doping on Structural, Optical and Electrical Properties of Ni1-xAgxO Thin Films Deposited by Spray Pyrolysis Technique

Study the Effect of Ni Doping on Structural, Optical and Electrical Properties of Ni1-xAgxO Thin Films Deposited by Spray Pyrolysis Technique

Correction: Effect of Ni dopant on the capacitive behavior of CuS for supercapacitor application

Correction: Effect of Ni dopant on the capacitive behavior of CuS for supercapacitor application

Effects of Ni2+ doping on magnetic and magnetoelectric properties of Y-type hexaferrite BaSrCo2Fe11AlO22

Magnetoelectric hexaferrites are the promising candidate materials for low-consumption magnetic memory device application, due to the existence of room-temperature magnetoelectric effect and the tunable magnetic structure. In this work, we studied the Ni doping effect on a rare room-temperature multiferroic BaSrCo2Fe11AlO22. With the comprehensive study of magnetism, magnetoelectricity, and ferroelectric properties, magnetoelectric phase diagrams of BaSrCo2-xNixFe11AlO22 were established. Generally, Ni doping has two important effects on magnetic and magnetoelectric properties. One is to strengthen superexchange interactions, greatly enhancing magnetic order temperature. Another effect is to destabilize the noncollinear magnetic structure at high temperature, causing the absence of ME effect at room temperature. In addition, the converse ME effects have been studied, revealing that converse ME coupling strength become weakened with the increase in Ni concentration. Our systematic studies provide important clues for synthesizing high performance magnetoelectric hexaferrites.

Evaluation on Mechanical Properties and Electrical Contact Behaviors for Au/Ni Composite Coating by Experiment and Finite Element Method

Gold coatings are the most widely used protective layer for resisting surface oxidization and corrosion in various complex environments. However, the extremely low hardness, inferior load‐bearing capacity, and lack of an effective strategy for evaluating the elastic‐plastic behavior of gold coatings have greatly limited their further application. The main aim of this work is to investigate the effect of Ni doping on the microstructure, mechanical properties, and electrical contact stability of a coating based on an experimental method and finite element simulation. The strain‐hardening exponent model of the coating is established by employing a reverse analysis method based on the nanoindentation experiment until the reverse and forward loading curves are consistent, thereby determining the yield strength. The results indicate that Ni doping is conducive to enhancing the mechanical properties under the premise of ensuring low contact resistance. The hardness (3.3–4.2 GPa) and yield strength (524.3–689.8 MPa) of the Au1−xNix composite coating with a Ni content of 4 at–8 at% is more than twice as high as that of pure Au. The electrical contacts deposited by the Au1−xNix coatings maintain a low contact resistance range (1.12–3.29 mΩ) at a contact force of 10 gf.

Synthesis, structural and magnetic characterizations of Li4Cu1-xNixTeO6 ( [formula omitted] = 0, 0.1, 0.2, 0.5, and 1)

We investigated the effect of Ni doping in a recently proposed quantum spin liquid (QSL) candidate Li4CuTeO6. We performed a comprehensive study on the structural and magnetic properties. We find that the anti-site disorder between Li+ and Cu2+ persists until 50% Ni doping in which Ni and Cu occupy different crystallographic sites. As a result, while Cu sits in both triangular and honeycomb layers in Li4CuTeO6, Ni forms only honeycomb layer in Li4NiTeO6 and Li4Cu0.5Ni0.5TeO6. Our magnetic susceptibility measurements show that the Weiss temperature decreases from -145.68 K in Li4CuTeO6 to -6.15 K in Li4NiTeO6 as Ni doping increases, and find no hint of magnetic ordering or freezing down to 1.8 K. Our analysis implies the existence of abundant low energy excitations in these materials.

Effect of Ni doping on mechanical properties and phase transformation in Co–V–Ga high-temperature shape memory alloys

In the present work, the effects of Ni doping on the microstructure and mechanical properties of Co–V–Ga high-temperature shape memory alloy have been studied. It has been found that γ phase occurs in the form of precipitation or even dendrite microstructure when Ni content continuously increases in the alloy. The composition distribution showed the elements Co and Ni segregated in the γ phase, while elements V and Ga concentrated in the martensite phase. Moreover, the phase transition temperature increased by Ni-doping in Co–V–Ga alloys due to the increase in e/a of the alloy. However, the abundant presence of γ phase hindered the shear phase transformation and created a large number of grain boundaries to reduce Ms temperature when Ni content continuously increased. In addition, electron backscattered diffraction (EBSD) results verified that the presence of γ phase could hinder the expansion of cracks, and improve the strength and plasticity of the alloy. Furthermore, it could be found the shape memory effect could maintain a relatively high recovery rate when Ni content was within a certain extent. However, the shape memory effect of the alloy significantly decreased in the presence of γ phase with dendrite microstructure. The current research results not only clarify the influence of Ni doping on the microstructure and mechanical behavior of Co–V–Ga alloys, but also provide guidance for element doping to prepare high-temperature shape memory alloys (HTSMAs) with excellent performance.

Effect of Ni dopant on the capacitive behavior of CuS for supercapacitor application

Effect of Ni dopant on the capacitive behavior of CuS for supercapacitor application