Nickel Nanoparticles Research Articles

Alternative Metallic Fillers for the Preparation of Conductive Nanoinks for Sustainable Electronics

AbstractThe development of electronics with net zero carbon emissions through more efficient and environmentally friendly materials and processes is still a challenge. Here, alternative chemical synthesis routes of metal conductive nanoparticles, based on biodegradable materials are explored, such as nickel, iron–nickel alloy and iron nanoparticles, to be used, in the long term, as fillers in inks for inject printing. Thus, Ni and FeNi metal nanoparticles of 25–12 nm, forming aggregates of 614–574 nm, respectively, are synthesized in water in the presence of a polyol and a reducing agent and under microwave heating that enables a more uniform and fast heating. Iron nanoparticles of 120 ± 40 nm are synthesized in polyol that limits the aggregation and the oxidation degree. Commercial metal nanoparticles of iron and nickel, are coated with ethylene glycol and used for comparison. The conductivity of nanoparticles when pressed into pellets remains similar for both commercial and synthesized samples. However, when deposited on a strip line and heated, synthesized Ni, FeNi, and Fe nanoparticles show significant conductivity and interesting magnetic properties. It is demonstrated that the nanosize facilitates sintering at reduced temperatures and the capping agents prevent oxidation, resulting in promising conductive fillers for printed electronic applications.

Electrochemical ammonia oxidation on terephthalic acid framework (BDC-NH2) derived core-shell nickel oxide/nickel-enriched 2D carbon nanoflakes (NiO/Ni/CNF)

A terephthalic framework, Ni-BDC-NH2, was used to synthesize the nickel nanoparticles and nanoclusters on-site encapsulated within mesoporous carbon nanoflakes (NiO/Ni/CNF) for ammonia electrolysis. Ni2+ nodes recrystallized to form a core-shell oxide film covering the Ni metal, with the dispersity and particles size influenced by the pyrolysis temperature in a N2 atmosphere. Electrochemical characterization and Raman spectra identified the solid-state Ni(II)⇌Ni(III) transition as the electron mediator, while its lowered onset potential (+1.3 V vs. RHE), compared to that of oxygen evolution reaction (+1.7 V) enhanced the Faradaic efficiency. The performance of electrodes in ammonia oxidation was assessed, which revealed a N2 selectivity of at least 80 % under electrolytic conditions of current density = 0.5 – 1.5 mA cm−2, pH > 10, and initial NH3 level = 50–300 mg-N L−1 using NiO/Ni/CNF(700). An undivided cell equipped with NiO/Ni/CNF(700) anode and Cu/Ni cathode was utilized to treat a real wastewater (∼500 mg-N L−1, pH 4.5). Consequently, both the removal efficiency of NH3 and N2 selectivity surpassed 90 % in a continuous flow mode for 4 days, indicating the durability of electrode system.

The crucial role of casein on crystal structure, size, morphology, and magnetic properties of carbon supported Ni nanoparticles

Carbon supported nonprecious metal nanoparticles have gained significant attention for their low cost and excellent properties. However, immobilizing them with good dispersion on carbon supports is still a great challenge. Herein, we report a simple and low cost thermal decomposition method to prepare a high quality carbon supported nickel nanoparticles in presence of casein as carbon source. By optimizing the concentration of carbon source, engineered the particle size from 50 nm to 17 nm and morphology from pyramid to spherical. Further, the impacts of morphology and particle size on the magnetic properties of these nanoparticles are studied. Moreover, thermally stable, biocompatible, low cost with unique magnetic properties makes these materials as potential candidate for various applications including chemisorbers, sensor, and electrochemical uses.

Morphology and electrical conductivity of carbon-coated Nickel reinforced high-performance polymer nanocomposites

Novel nanocomposites of poly (ether-ketone) (PEK) reinforced with carbon-coated Nickel nanoparticles (CCNi) were synthesized through a sequential process involving cost-effective ball milling and hot compaction. Scanning electron microscopy revealed an excellent dispersion and a three-dimensional network of CCNi nanoparticles in the matrix, causing a significant improvement in the electrical conductivity and electromagnetic interference shielding effectiveness (SE). Carbon coating of about 5 nm thick over Ni nanoparticle probably helps in uniform dispersion, avoids its oxidation and reduces its agglomeration in the matrix. An exceptionally low percolation threshold of 2.1 vol.% CCNi was found, and eight-orders of magnitude enhancement in the dc-electrical conductivity was achieved. The highest dc- and ac-electrical conductivities achieved were more than 0.01 S cm−1 at 5.89 vol.% CCNi nanoparticles content which were the highest values amongst reported Ni-filled polymer composites and comparable with those of carbon nanotubes filled PEK nanocomposites. Electromagnetic interference SE of the CCNi/PEK nanocomposites was measured in the X-band, and a total SE (SET) of 17.52 dB was obtained for 5.89 vol.% CCNi reinforced PEK nanocomposite.

In-situ construction of iron-modified nickel nanoparticles assisted by hexamethylenetetramine with the internal and external collaboration for highly selective electrocatalytic carbon dioxide reduction

Carbon dioxide (CO2) electroreduction provides a sustainable route for realizing carbon neutrality and energy supply. Up to now, challenges remain in employing abundant and inexpensive nickel materials as candidates for CO2 reduction due to their low activity and favorable hydrogen evolution. Here, the representative iron-modified nickel nanoparticles embedded in nitrogen-doped carbon (Ni1-Fe0.125-NC) with the porous botryoid morphology were successfully developed. Hexamethylenetetramine is used as nitrogen-doped carbon source. The collaboration of internal lattice expansion with electron effect and external confinement effect with size effect endows the significant enhancement in electrocatalytic CO2 reduction. The optimized Ni1-Fe0.125-NC exhibits broad potential ranges for continuous carbon monoxide (CO) production. A superb CO Faradaic efficiency (FECO) of 85.0 % realized at −1.1 V maintains a longtime durability over 35 h, which exceeds many state-of-the-art metal catalysts. Theoretical calculations further confirm that electron redistribution promotes the desorption of CO in the process for favorable CO production. This work opens a new avenue to design efficient nickel-based materials by considering the intrinsic structure and external confinement for CO2 reduction.

Nanohybrids with potential barrier property and antimicrobial activity for application in sustainable polymer food packaging: A mini‐review

AbstractPackaging has important functions for products, contributing to their protection and presenting information. Recognizing that food loss and waste affect all countries, it is necessary to search for alternatives that change this scenario, such as active packaging. Particles with sizes between 1 and 100 nanometers (nanoparticles) are incorporated into polymeric materials because they are capable of improving or even providing properties that the film formed by the pure polymer does not have, due to its surface area being greater than that of macro‐sized particles. If two nanoparticles are previously combined to form a nanohybrid before being dispersed in a polymeric matrix, in addition to having this purpose, they can provide even better results when incorporated, due to the synergistic effects that can be attributed to the nanoparticles used. The utilization of active packaging composed of nano‐hybrids within biodegradable polymers holds significant potential for reducing solid plastic waste and the generation of persistent microplastics, thereby positively impacting human health. In this literature review, the effects of nanohybrid on antibacterial and barrier properties for application in food packaging in polymeric matrices were investigated using materials such as: nickel nanoparticles, zinc oxide nanoparticles, silver nanoparticles, copper oxide nanoparticles, cellulose nanowhiskers, Cloisite 30B, sodium alginate, poly(ethylene oxide), starch, poly(vinyl alcohol), chitosan and gelatin. The results were found to show the efficiency of nanohybrids in polymeric matrices, decreasing the water vapor and oxygen permeability and also increasing the antibacterial activity, which can prevent illnesses stemming from contaminated food occurs.

Furfural Hydrogenation Over Reduced Pure (LaBO3) and Substituted (LaB0.5B'0.5O3) (B, B': Fe, Co, Ni) Perovskites

AbstractA series of pure and 50 % substituted Fe‐containing (LaFeO3, LaFe0.5Ni0.5O3 and LaFe0.5Co0.5O3) and Co/Ni‐containing (LaCoO3, LaNiO3, and LaCo0.5Ni0.5O3) perovskites were used as precursors to synthesize metallic reduced catalysts to be tested for the liquid hydrogenation of furfural. The catalytic reaction was carried out in a batch reactor at 200 °C and 3.0 MPa of H2 pressure. The calcined perovskites and reduced catalysts were characterized by X‐ray diffraction (XRD), N2 physisorption at 77 K, temperature programmed reduction (H2‐TPR), temperature programmed CO2 and NH3 desorption (CO2‐TPD and NH3‐TPD), Atomic Absorption Spectroscopy (AAS) and X‐ray photoelectron spectroscopy (XPS) techniques. The LaCo0.5Ni0.5O3 reduced catalyst display the highest activity in furfural conversion, which was attributed to a cooperative effect between highly dispersed nickel and cobalt metal nanoparticles after reduction process. The effect of the nature of B‐cation have a high impact on the products selectivity in the hydrogenation of furfural, suggesting that enriched‐Ni metal surface was selectivity to tetrahydrofurfuryl alcohol, meanwhile enriched‐Co metal surface was selective to furfuryl alcohol formation, which was also supported with adsorption mode of furfural over the active sites obtained by quantum calculation.

Plant-Based Extracts as Reducing, Capping, and Stabilizing Agents for the Green Synthesis of Inorganic Nanoparticles

The synthesis of inorganic nanoparticles for diverse applications is an active research area that involves physical and chemical methods, which typically are expensive, involve hazardous chemical reagents, use complex equipment and synthesis conditions, and consume large amounts of time and energy. Thus, green synthesis methods have emerged as eco-friendly and easy alternatives for inorganic nanoparticle synthesis, particularly the use of plant-based extracts from fruit juice, leaves, seeds, peel, stem, barks, and roots, which act as reducing, capping, and stabilizing agents, contributing to the Sustainable Development Goals and circular economy principles. Therefore, diverse inorganic nanoparticles have been synthesized using plant-based extracts, including gold, silver, titanium dioxide, zinc, copper, platinum, zirconium, iron, selenium, magnesium, nickel, sulfur, cobalt, palladium, and indium nanoparticles, which exhibit different biological activities such as antioxidant, antimicrobial, dye degradation, cytotoxic, analgesic, sedative, wound-healing, skin protection, sensor development, and plant-growth-promoting effects. Therefore, this review summarizes the advantages and limitations of plant-based extracts as reducing, capping, and stabilizing agents for inorganic nanoparticle green synthesis.

Exploring the effective adsorption of polystyrene microplastics from aqueous solution with magnetically separable nickel/reduced graphene oxide (Ni/rGO) nanocomposite.

Microplastics (MPs) are a potential threat to both humans and aquatic environment as they serve as carriers of various contaminants necessitating the development of reliable, efficient, and ecofriendly techniques to remove MPs from water. In this study, reduced graphene oxide (rGO) magnetized using nickel nanoparticles was utilized as a potent adsorbent for the effective removal of microplastics from water. The synthesized nickel/reduced graphene oxide (Ni/rGO) nanocomposite was characterized by X-ray diffraction (XRD), Raman spectra, vibrating sample magnetometer (VSM), scanning electron microscopy-energy-dispersive X-ray analysis (SEM-EDX), thermogravimetric analysis, and Brunauer-Emmett Teller (BET) analysis. Magnetic Ni/rGO nanocomposite exhibited significant adsorption capability for polystyrene (PS) microspheres allowing the formation of PS-Ni/rGO complex which can be easily separated out using a magnet. The SEM images of PS-Ni/rGO complex confirmed the adsorption of PS microspheres onto the nano adsorbent due to hydrophobic interaction. The adsorbent demonstrated a maximum adsorption capacity of 1250mg/g. The analysis of isotherm and kinetic models demonstrated that the adsorption mechanism conformed to the Langmuir isotherm and followed pseudo second order kinetics. This study paves a new pathway for the application of magnetically modified reduced graphene oxide for the expedient removal of microplastics from water with the ease of separation using a magnet. The adsorbent was recycled and reused for three times.

Steering bidirectional polysulfide conversion in virtue of interface microenvironment of Ni/porous carbon Mott-Schottky heterojunctions

Originating from the notorious shuttle effect and intrinsically sluggish redox kinetics of polysulfides (especially under the conditions of high sulfur loadings and low electrolytes), the low capacity and sulfur utilization efficiency, unsatisfactory rate performance, and unremarkable cycle performance severely hinder the practical commercialization of lithium-sulfur batteries (LSBs). Furnishing rapid electron transfer and mass diffusion in virtue of interface modulation and nanostructure design is an effective strategy to enhance the activity of catalysts. Herein, a Mott-Schottky heterojunction composed of porous carbon (PC)-supported nickel (Ni) nanoparticles was fabricated on a functionalized carbon nanotube sponge (Ni/PC/FCNTS) via adjusting the geometric structure such as the particle size, aggregation state and pore volume (based on the different solvothermal reaction temperature of the Ni-MOF precursor and the high-temperature pyrolysis process). Transmission electron microscope (TEM) and X-ray photoelectron spectroscopy (XPS) demonstrated the charge redistribution and a self-generated built-in electric field accelerated electron transfer at the heterogeneous interface between Ni and PC. Meanwhile, the high pore volume of Ni/PC/FCNTS-170 provided a reaction space for rapid ion diffusion and sulfur redox process. Benefiting from the synergistic effect, the derived S@Ni/PC/FCNTS-170 cells manifested excellent rate performance with a capacity of 784.2 mAh g-1 at 2 C and a high areal capacity of 8.09 mAh cm-2 with a high sulfur loading of 17.6 mg cm-2 and low electrolyte/sulfur of 11.3 µL mg-1.

Toward an Improved Electrocatalytic Determination of Immunomodulator COVID Medication Baricitinib Using Multiwalled Carbon Nanotube Nickel Hybrid.

The study presents a first electrochemical method for the determination of the immunomodulator drug Baricitinib (BARI), crucial in managing COVID-19 patients requiring oxygen support. A unique electrode was developed by modifying graphite carbon nickel nanoparticles (NiNPs) with functionalized multiwalled carbon nanotubes (f.MWCNTs), resulting in nanohybrids tailored for highly sensitive BARI detection. Comparative analysis revealed the superior electrocatalytic performance of the nanohybrid-modified electrode over unmodified counterparts and other modifications, attributed to synergistic interactions between f.MWCNTs and nickel nanoparticles. Under optimized conditions, the sensors exhibited linear detection within a concentration range from 4.00 × 10-8 to 5.56 × 10-5 M, with a remarkably low detection limit of 9.65 × 10-9 M. Notably, the modified electrode displayed minimal interference from common substances and demonstrated high precision in detecting BARI in plasma and medicinal formulations, underscoring its clinical relevance and potential impact on COVID-19 treatment strategies.

Catalytic degrading agents for dyes from pyrimidine derived imine capped nickel nanoparticles: Colorization of cotton and antibacterial activity of colored cotton

In this multifaceted experimental study, Schiff base (SL) stabilized nickel nanoparticles (SL-NiNPs) were synthesized and comprehensively characterized for their diverse applications. The synthesis process involved the formation of these nanoparticles through the reduction of ethanolic nickel chloride with sodium borohydride (NaBH4) under nitrogen gas, followed by their stabilization in toluene using tetraoctylammonium bromide (TOAB) as phase transfer agent and SL as capping agent. Characterization studies confirmed the successful synthesis and stabilization of SL-NiNPs, with UV-Vis spectral analysis, SEM, and TEM revealing their distinctive properties, including a spherical shape and a size of approximately 50 nm. The catalytic properties of SL-NiNPs was demonstrated in several reactions, including the reduction of 4-nitrophenol to 4-aminophenol, the degradation of methylene blue, and the reduction of methyl orange. These catalytic reactions showcased the efficiency and versatility of SL-NiNPs as effective catalysts for environmental and chemical processes. Furthermore, SL-NiNPs were employed in the coloration of cotton, leading to surface modification with nano-sized particles. SEM imaging illustrated the successful modification of cotton, enhancing its surface properties. The antimicrobial potential of SL-NiNPs-embedded cotton was assessed against various bacterial strains, revealing a dose-dependent inhibitory effect. As the concentration of SL-NiNPs increased, the diameter of the inhibition zones also increased, further emphasizing the potent antibacterial properties of these materials.

Ruthenium–Nickel Nanoparticles with Unconventional Face‐Centered Cubic Crystal Phase for Highly Active Electrocatalytic Hydrogen Evolution

AbstractRu‐based nanomaterials are promising alternatives to Pt electrocatalysts for green hydrogen energy generation, and crystal phase engineering holds the key to unlocking their catalytic potential to new heights. However, controllable phase regulation on Ru‐alloys remains a formidable challenge, and unraveling the crystal phase‐related electrocatalytic performance is of great significance. Herein, RuNi nanoparticles are successfully synthesized with an unconventional face‐centered cubic (fcc) phase via a facile route. Comprehensive transmission electron microscopy confirmed the structural characteristics of the fcc‐RuNi and electrochemical analyses indicate the impressive electrocatalytic hydrogen evolution reaction of fcc‐RuNi. Notably, the anomalous fcc‐RuNi nanoparticles possess an extraordinarily low overpotential of 16 mV in hydrogen evolution. Density functional theory calculations indicate that these nanoparticles are energetically conducive to intermediate desorption and H2O dissociation. This study enhances comprehension of phase regulation in Ru‐based nanostructures and will propel phase engineering in diverse catalytic applications.

Electrochemical Synthesis of Hollow Nanoparticles via Anodic Transformation of Metastable Core-Shell Precursors.

Recent advances in electrosynthesis of nanomaterials expanded structural and compositional variations accessible by the electrochemical method; however, reliably synthesizable morphological variety fall shy of that available by conventional solvothermal synthesis. In this communication, electrochemical preparation of surfactant-free hollow nanoparticles is demonstrated. By anodic conversion of core-shell precursors with metastable cores, hollowed nickel nanoparticles with uniform dimensions were synthesized and characterized. Implementation of TEM grids as the working electrodes, identical location tracking of the morphological evolution of single particles to anodic stimulus has been demonstrated. The synthesized nanoparticles were employed as catalysts for the alkaline hydrogen evolution reaction and exhibited catalytic rates that compare favorably to the Pt/C benchmark. This marks the first pure electrochemical synthesis of hollow nanoparticles and shall contribute to the structural diversification of electrosynthesized nanomaterials.

Bioaccessibility of Metallic Nickel and Nickel Oxide Nanoparticles in Four Simulated Biological Fluids

Bioaccessibility of metals from substances and alloys is increasingly used as part of the assessment to predict potential toxicity. However, data are sparse on the metal bioaccessibility from nanoparticle (NP) size metal substances. This study examines nickel ion release from metallic nickel and nickel oxide micron particles (MPs) and NPs in simulated biological fluids at various timepoints including those relevant for specific routes of exposure. The results suggest that MPs of both metallic nickel and nickel oxide generally released more nickel ions in acidic simulated biological fluids (gastric and lysosomal) than NPs of the same substance, with the largest differences being for nickel oxide. In more neutral pH fluids (interstitial and perspiration), nickel metal NPs released more nickel ions than MPs, with nickel oxide results showing a higher release for MPs in interstitial fluid yet a lower release in perspiration fluid. Various experimental factors related to the particle, fluid, and extraction duration were identified that can have an impact on the particle dissolution and release of nickel ions. Overall, the results suggest that based on nickel release alone, nickel NPs are not inherently more hazardous than nickel MPs. Moreover, analyses should be performed on a case-by-case basis with consideration of various experimental factors and correlation with in vivo data.

Physiological and molecular responses of the copepods Acartia clausi and Acartia tonsa to nickel nanoparticles and nickel chloride

Nickel compounds in dissolved form or as nanoparticles may affect planktonic invertebrates in marine ecosystems. Here, we assessed the physiological (naupliar mortality, egg production, egg hatching success) and molecular (quantitative gene expression) responses of the crustacean copepods Acartia clausi (indigenous Mediterranean species) and Acartia tonsa (model organism in ecotoxicology), to nickel nanoparticles (NiNPs) and nickel chloride (NiCl2), over time. We also measured NPs size and the temporal release of Ni ions in aqueous solution, through dynamic light scattering (DLS) and inductively coupled plasma-mass spectrometry (ICP-MS), respectively.Nauplii of A. clausi were highly vulnerable to NiCl2 in the 48 h acute test, with an EC50 in the range of Ni concentrations measured in polluted waters. Females of both species exhibited a decreased egg production and hatching success after the 4-day exposure to NiNPs. Molecular responses in A. clausi incubated in NiNPs and NiCl2 showed a stronger up- or down-regulation, compared to A. tonsa, of genes associated with detoxification (phospholipid-hydroperoxide glutathione peroxidase, glutathione-S-transferase sigma), oxidative stress (superoxide dismutase), nervous system functioning (acetylcholinesterase), and oogenesis (vitellogenin).In conclusion, new information was here obtained on the effects of different forms of nickel on physiological and molecular responses of A. clausi, that could help to identify biomarker genes of exposure to be used as early-warning indicators. Our results also highlighted the need of employing indigenous copepod species to better evaluate the ecotoxicological impact of pollutants in different geographical area.

Nephrotoxicity, Hepatotoxicity, and Blood Viscoelasticity Induced by Nickel Nanoparticles in Albino Rats

Nephrotoxicity, Hepatotoxicity, and Blood Viscoelasticity Induced by Nickel Nanoparticles in Albino Rats

Synergistic growth of nickel and platinum nanoparticles via exsolution and surface reaction

Bimetallic catalysts combining precious and earth-abundant metals in well designed nanoparticle architectures can enable cost efficient and stable heterogeneous catalysis. Here, we present an interaction-driven in-situ approach to engineer finely dispersed Ni decorated Pt nanoparticles (1-6 nm) on perovskite nanofibres via reduction at high temperatures (600-800 oC). Deposition of Pt (0.5 wt%) enhances the reducibility of the perovskite support and promotes the nucleation of Ni cations via metal-support interaction, thereafter the Ni species react with Pt forming alloy nanoparticles, with the combined processes yielding smaller nanoparticles that either of the contributing processes. Tuneable uniform Pt-Ni nanoparticles are produced on the perovskite surface, yielding reactivity and stability surpassing 1 wt.% Pt/γ-Al2O3 catalysts for CO oxidation. This approach heralds the possibility of in-situ fabrication of supported bimetallic nanoparticles with engineered compositional distributions and performance.

Antibacterial Activity of Nickel Nanoparticles Against Pathogenic Bacteria

Antibacterial Activity of Nickel Nanoparticles Against Pathogenic Bacteria

Nickel-Induced Reduced Graphene Oxide Nanoribbon Formation on Highly Ordered Pyrolytic Graphite for Electronic and Magnetic Applications.

The development of nanoribbon-like structures is an effective strategy to harness the potential benefits of graphenic materials due to their excellent electrical properties, advantageous edge sites, rapid electron transport, and large specific area. Herein, parallel and connected magnetic nanostructured nanoribbons are obtained through the synthesis of reduced graphene oxide (rGO) using NiCl2 as a precursor with potential applications in nascent electronic and magnetic devices. Several analytical techniques have been used for the thorough characterization of the modified surfaces. Atomic force microscopy (AFM) shows the characteristic topographical features of the nanoribbons. While X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), and Raman spectroscopy provided information on the chemical state of Ni and graphene-like structures, magnetic force microscopy (MFM) and scanning Kelvin probe microscopy (SKPFM) confirmed the preferential concentration of Ni onto rGO nanoribbons. These results indicate that the synthesized material shows 1D ordering of nickel nanoparticles (NiNPs)-decorating tiny rGO flakes into thin threads and the subsequent 2D arrangement of the latter into parallel ribbons following the topography of the HOPG basal plane.