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Background Previous studies have demonstrated that exposure to nickel nanoparticles (Nano-Ni) causes oxidative stress and severe, persistent lung inflammation, which are strongly associated with pulmonary toxicity. However, few studies have investigated whether surface modification of Nano-Ni could alter Nano-Ni-induced lung injury, inflammation, and fibrosis in vivo. Here, we propose that alteration of physicochemical properties of Nano-Ni through modification of Nano-Ni surface may change Nano-Ni-induced lung injury, inflammation, and fibrosis. Methods At first, dose–response and time-response studies were performed to observe lung inflammation and injury caused by Nano-Ni. In the dose–response studies, mice were intratracheally instilled with 0, 10, 20, 50, and 100 μg per mouse of Nano-Ni and sacrificed at day 3 post-exposure. In the time-response studies, mice were intratracheally instilled with 50 µg per mouse of Nano-Ni and sacrificed at days 1, 3, 7, 14, 28, and 42 post-instillation. At the end of the experiment, mice were bronchoalveolar lavaged (BAL) and the neutrophil count, CXCL1/KC level, LDH activity, and concentration of total protein in the BAL fluid (BALF) were determined. In the comparative studies, mice were intratracheally instilled with 50 μg per mouse of Nano-Ni or with the same molar concentration of Ni as Nano-Ni of either partially [O]-passivated Nano-Ni (Nano-Ni–P) or carbon-coated Nano-Ni (Nano-Ni–C). At day 3 post-exposure, BAL was performed and the above cellular and biochemical parameters in the BALF were analyzed. The MMP-2/9 protein levels and activities in the BALF and mouse lung tissues were also determined. Mouse lung tissues were also collected for H&E staining, and measurement of thiobarbituric acid reactive substances (TBARS) and 8-hydroxy-2′-deoxyguanosine (8-OHdG) in the genomic DNA. At day 42 post-exposure, mouse right lung tissues were collected for H&E and Trichrome stainings, and left lung tissues were collected to determine the hydroxyproline content. Results Exposure of mice to Nano-Ni resulted in a dose–response increase in acute lung inflammation and injury reflected by increased neutrophil count, CXCL1/KC level, LDH activity, and concentration of total protein in the BALF. The time-response study showed that Nano-Ni-induced acute lung inflammation and injury appeared as early as day 1, peaked at day 3, and attenuated at day 7 post-instillation. Although the neutrophil count, CXCL1/KC level, LDH activity, and concentration of total protein in the BALF dramatically decreased over the time, their levels were still higher than those of the controls even at day 42 post-exposure. Based on the results of the dose- and time-response studies, we chose a dose of 50 µg per mouse of Nano-Ni, and day 3 post-exposure as short-term and day 42 post-exposure as long-term to compare the effects of Nano-Ni, Nano-Ni–P, and Nano-Ni–C on mouse lungs. At day 3 post-exposure, 50 μg per mouse of Nano-Ni caused acute lung inflammation and injury that were reflected by increased neutrophil count, CXCL1/KC level, LDH activity, concentration of total protein, and MMP-2/9 protein levels and activities in the BALF. Nano-Ni exposure also caused increased MMP-2/9 activities in the mouse lung tissues. Histologically, infiltration of large numbers of neutrophils and macrophages in the alveolar space and interstitial tissues was observed in mouse lungs exposed to Nano-Ni. Nano-Ni–P exposure caused similar acute lung inflammation and injury as Nano-Ni. However, exposure to Nano-Ni–C only caused mild acute lung inflammation and injury. At day 42 post-exposure, Nano-Ni caused extensive interstitial fibrosis and proliferation of interstitial cells with inflammatory cells infiltrating the alveolar septa and alveolar space. Lung fibrosis was also observed in Nano-Ni–P-exposed lungs, but to a much lesser degree. Only slight or no lung fibrosis was observed in Nano-Ni–C-exposed lungs. Nano-Ni and Nano-Ni–P, but not Nano-Ni–C, caused significantly elevated levels of TBARS in mouse lung tissues and 8-OHdG in mouse lung tissue genomic DNA, suggesting that Nano-Ni and Nano-Ni–P induce lipid peroxidation and oxidative DNA damage in mouse lung tissues, while Nano-Ni–C does not. Conclusion Our results demonstrate that short-term Nano-Ni exposure causes acute lung inflammation and injury, while long-term Nano-Ni exposure causes chronic lung inflammation and fibrosis. Surface modification of Nano-Ni alleviates Nano-Ni-induced pulmonary effects; partially passivated Nano-Ni causes similar effects as Nano-Ni, but the chronic inflammation and fibrosis were at a much lesser degree. Carbon coating significantly alleviates Nano-Ni-induced acute and chronic lung inflammation and injury.

Background Nickel nanoparticles (Nano-Ni) are increasingly used in industry and biomedicine with the development of nanotechnology. However, the genotoxic and carcinogenic effects of Nano-Ni and the underlying mechanisms are still unclear. Methods At first, dose–response (0, 10, 20, and 30 μg/mL) and time-response (0, 3, 6, 12, and 24 h) studies were performed in immortalized normal human bronchial epithelial cells BEAS-2B to observe the effects of Nano-Ni on DNA damage response (DDR)-associated proteins and the HIF-1α/miR-210/Rad52 pathway by real-time PCR or Western blot. Then, a Hsp90 inhibitor (1 µM of 17-AAG, an indirect HIF-1α inhibitor), HIF-1α knock-out (KO) cells, and a miR-210 inhibitor (20 nM) were used to determine whether Nano-Ni-induced Rad52 down-regulation was through HIF-1α nuclear accumulation and miR-210 up-regulation. In the long-term experiments, cells were treated with 0.25 and 0.5 µg/mL of Nano-Ni for 21 cycles (~ 150 days), and the level of anchorage-independent growth was determined by plating the cells in soft agar. Transduction of lentiviral particles containing human Rad52 ORF into BEAS-2B cells was used to observe the role of Rad52 in Nano-Ni-induced cell transformation. Nano-Ni-induced DNA damage and dysregulation of HIF-1α/miR-210/Rad52 pathway were also investigated in vivo by intratracheal instillation of 50 µg per mouse of Nano-Ni. gpt delta transgenic mice were used to analyze mutant frequency and mutation spectrum in mouse lungs after Nano-Ni exposure. Results Nano-Ni exposure caused DNA damage at both in vitro and in vivo settings, which was reflected by increased phosphorylation of DDR-associated proteins such as ATM at Ser1981, p53 at Ser15, and H2AX. Nano-Ni exposure also induced HIF-1α nuclear accumulation, miR-210 up-regulation, and down-regulation of homologous recombination repair (HRR) gene Rad52. Inhibition of or knocking-out HIF-1α or miR-210 ameliorated Nano-Ni-induced Rad52 down-regulation. Long-term low-dose Nano-Ni exposure led to cell malignant transformation, and augmentation of Rad52 expression significantly reduced Nano-Ni-induced cell transformation. In addition, increased immunostaining of cell proliferation markers, Ki-67 and PCNA, was observed in bronchiolar epithelial cells and hyperplastic pneumocytes in mouse lungs at day 7 and day 42 after Nano-Ni exposure. Finally, using gpt delta transgenic mice revealed that Nano-Ni exposure did not cause increased gpt mutant frequency and certain DNA mutations, such as base substitution and small base insertions/deletions, are not the main types of Nano-Ni-induced DNA damage. Conclusions This study unraveled the mechanisms underlying Nano-Ni-induced cell malignant transformation; the combined effects of Nano-Ni-induced DNA damage and DNA repair defects through HIF-1α/miR-210/Rad52 pathway likely contribute to Nano-Ni-induced genomic instability and ultimately cell transformation. Our findings will provide information to further elucidate the molecular mechanisms of Nano-Ni-induced genotoxicity and carcinogenicity. Graphical Abstract

Advances in fuel cell technology depend strongly on the development of affordable, active, and stable catalysts. For example, octahedral Pt-Ni alloy nanoparticles show exceptional activity for the oxygen reduction reaction in fuel cell cathodes as a result of the presence of highly active {1 1 1} facets. Here, we review a selection of recent transmission electron microscopy studies that address the correlation between the catalytic performance of octahedral Pt-Ni-based nanoparticles and their atomic-scale structure and composition. We begin by describing strategies for the growth of binary Pt-Ni and ternary Pt-Ni-TM (TM = transition metal) nanoparticles, with a focus on understanding how their structure and compositional anisotropy is related to their catalytic activity and stability. We then describe the morphological changes and compositional degradation effects that can occur in electrochemical environments. Changes in nanoparticle shape, including the loss of highly active {1 1 1} facets due to dealloying from Ni-rich facets and Pt surface diffusion, are discussed as important reasons for catalyst degradation. Finally, strategies to prevent degradation, e.g. by surface doping, are addressed. The growth, segregation, and degradation mechanisms that we describe highlight the complexity with which octahedral alloy nanoparticles form and evolve under reaction conditions.

In this study, trimetallic catalysts were prepared via the co-precipitation and impregnation methods. In order to investigate the effect of impregnation on the catalytic activity and crystallite size, a trimetallic catalyst, Fe—Ni—Ce, was prepared through the co-precipitation method in one set of experiments, and cerium was impregnated with the Ni—Fe mixture in the final stage of the preparation in another set. Fourier transform infrared spectroscopy was employed to confirm the formation of trimetallic catalysts and the success of the impregnation method. The Brunauer-Emmett-Teller nitrogen adsorption isotherm exhibits a high specific surface area (approximately 39 m 2 g −1 ) for the nanoparticles obtained by the impregnation method. The crystallography and morphology of the trimetallic catalysts thus prepared were characterised by X-ray diffraction and scanning electron microscopy. UV-VIS spectroscopy and methylene blue dye degradation tests were also performed to investigate the catalytic activity of the synthesised catalysts. The crystalline size was found to be smaller for the catalysts prepared by the impregnation method. In addition, the samples synthesised using the cerium impregnation method showed superior activity in the methylene blue dye degradation test. The effect of the catalyst dosage on dye degradation, as well as the effect of the initial dye concentration on the catalyst activity, was also studied for both methods.

This study aims to explore the underutilized potential of Persea americana (avocado) peel extract as a green reducing and stabilizing agent for the synthesis of bimetallic nanoparticles (BMNPs), specifically Cu–Ag, Ni–Cu, and Ni–Ag. Using no external chemicals, BMNPs were synthesized through an eco‐friendly route and evaluated for their physicochemical properties and antibacterial efficacy. Optimized synthesis conditions (pH 10, 80°C, 1 h, 1:1 metal ratio, 20 mL extract) yielded air stable nanoparticles with dual surface plasmon resonance peaks: 396/591 nm (Ag–Cu), 417/592 nm (Ag–Ni), and 363/418 nm (Cu–Ni), indicating the presence of multiple metallic species. FTIR analysis confirmed the involvement of bioactive functional groups (‐OH, ‐COOH, ‐NH) in metal ion reduction and nanoparticle stabilization. PXRD confirmed the formation of crystalline bimetallic alloys not core–shell or mixed‐phase structures with sizes of 37 nm (Ag–Cu), 11.21 nm (Ag–Ni), and 20.63 nm (Cu–Ni), while SEM revealed nonspherical BMNPs measuring 35.5, 11.5, and 25.5 nm, respectively. The BMNPs were tested against Gram‐positive (GP) and Gram‐negative (GN) bacteria, including E. coli , P. aeruginosa , S. aureus , and S. pyogenes . Antibacterial assays, with amoxicillin as a positive control and DMSO as solvent, revealed greater efficacy against GP strains. Notably, Cu–Ni BMNPs exhibited the strongest activity against Streptococcus pyogenes , with the highest inhibition zone (12.50 ± 0.41 mm, p < 0.05). These findings highlight avocado peel‐derived BMNPs as promising, sustainable antimicrobial agents, offering a green alternative to conventional nanoparticle synthesis for combating resistant pathogens.

Li‐CO2 batteries could skillfully combine the reduction of “greenhouse effect” with energy storage systems. However, Li‐CO2 batteries still suffer from unsatisfactory electrochemical performances and their rechargeability is challenged. Here, it is reported that a composite of Ni nanoparticles highly dispersed on N‐doped graphene (Ni‐NG) with 3D porous structure, exhibits a superior discharge capacity of 17 625 mA h g−1, as the air cathode for Li‐CO2 batteries. The batteries with these highly efficient cathodes could sustain 100 cycles at a cutoff capacity of 1000 mA h g−1 with low overpotentials at the current density of 100 mA g−1. Particularly, the Ni‐NG cathodes allow to observe the appearance/disappearance of agglomerated Li2CO3 particles and carbon thin films directly upon discharge/charge processes. In addition, the recycle of CO2 is detected through in situ differential electrochemical mass spectrometry. This is a critical step to verify the electrochemical rechargeability of Li‐CO2 batteries. Also, first‐principles computations further prove that Ni nanoparticles are active sites for the reaction of Li and CO2, which could guide to design more advantageous catalysts for rechargeable Li‐CO2 batteries. A composite of Ni nanoparticles highly dispersed on N‐doped graphene is prepared as the air cathode for Li‐CO2 batteries, with high discharge capacity and excellent cyclic stability. The cathode allows to observe the morphological evolution of discharge products directly and reversible consumption and evolution of CO2, and then the reversibility of electrochemical reactions could well be understood in Li‐CO2 batteries.

This study investigates the effect of minor additions of Ni, Ni3Sn or Ni3Sn2 nanoparticles on the microstructure and mechanical properties of Cu/solder/Cu joints. The nanocomposite Sn-3.0Ag-0.5Cu (SAC305) solders with 0.5, 1.0 and 2.0 wt.% metallic nanoparticles were prepared through a paste mixing method. The employed Ni and Ni-Sn nanoparticles were produced via a chemical reduction method. The microstructure of as-solidified Cu/solder/Cu joints was studied by x-ray diffraction and scanning electron microscopy. The results showed that additions of Ni and Ni-Sn nanoparticles to the SAC305 solder paste lead initially to a decrease in the average thickness of the intermetallic compound layer in the interface between solder and substrate, while further additions up to 2.0 wt.% did not induce any significant changes. In addition, shear strength and microhardness tests were performed to investigate the relationship between microstructure and mechanical properties of the investigated solder joints. The results indicated an increase in both of these properties which was most significant for the solder joints using SAC305 with 0.5 wt.% Ni or Ni-Sn nanoparticles.

Searching for inexpensive, efficient and durable electrocatalysts with earth-abundant elements toward the hydrogen evolution reaction (HER) is of vital importance for the future sustainable hydrogen economy, yet still remains a formidable challenge. Herein, a facile template-engaged strategy is demonstrated for the direct in-situ growth of Ni nanoparticles and N-doped carbon nanotubes on carbon nanorod substrates, forming a hierarchically branched architecture (abbreviated as Ni@N-C NT/NRs hereafter). The elaborate construction of such unique hierarchical structure with tightly encapsulated Ni nanoparticles and open configuration endows the as-fabricated Ni@N-C NT/NRs with abundant well-dispersed active sites, enlarged surface area, reduced resistances of charge transfer and mass diffusion, and reinforced mechanical robustness. As a consequence, the optimal Ni@N-C NT/NR catalyst demonstrates superior electrocatalytic activity with relatively low overpotential of 134 mV to deliver a current density of 10 mA·cm −2 and excellent stability for HER in 0.1 M KOH, holding a great promise for practical scalable H 2 production. More importantly, this work offers a reliable methodology for feasible fabrication of robust high-performance carbon-based hierarchical architectures for a variety of electrochemical applications.

Developing non-noble and high-performance metal hydrogen evolution reaction (HER) electrocatalysts is significant for hydrogen production. Doping heteroatoms on the surface of graphene is another amazing measure to improve the catalytic behavior of catalysts. In this work, halogen-doped reduced graphene oxide with nickel nanoparticles (Ni-XRGO) was investigated as an innovative electrocatalyst for the HER. The scanning electron microscopy images of the Ni-XRGO catalyst showed the leaf-like structure morphology with wide distribution. Also, the energy-dispersive X-ray spectroscopy, mapping technique, confirmed that the presence of halogens caused the homogenous distribution of Ni nanoparticles. X-ray diffraction technique confirmed the presence of doped halogens in reduced graphene oxide. The Ni-XRGO electrode with only 61 mV vs. RHE onset potential, 41 mV dec −1 Tafel slope, good lifetime stability, and low charge transfer resistance could be a promising cathodic electrode for catalysis of HER. The particular electrochemical performance is due to the influence of the halogen elements on the charge distribution of the graphene surface; this leads to an enhancement in the exposure of additional active sites and an extension of the electrochemical active area. Our study presents a novel approach to the development of non-precious metal electrocatalysts that are both highly efficient and cost-effective for HER.

Noble‐metal free, cost‐effective, and highly stable catalysts with efficient activity for both the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER) have attracted tremendous research interest in recent years. Here, a flexible, self‐standing hybrid film comprising a N‐doped single‐wall carbon nanotube (SWCNT) network on which are anchored Ni nanoparticles encapsulated by a monolayer of N‐doped carbon (NCNi) is reported. The films are prepared by floating catalyst chemical vapor deposition followed by NH3 treatment. The material obtained at optimum conditions shows excellent bifunctional electrocatalytic activity in alkaline media with low overpotentials of 190 and 270 mV for HER and OER, respectively, to reach a current density of 10 mA cm−2. A current density of 10 mA cm−2 at 1.57 V is achieved when this freestanding and binder‐free rod‐shaped NCNi/SWCNT assembly is used as cathode and anode in 1 m KOH solution for overall water splitting, presenting one of the best values reported to date. A support‐free film of single‐wall carbon nanotubes decorated with small‐sized Ni nanoparticles covered by N‐doped monolayer carbon shows excellent electrocatalytic activity at low overpotentials for overall water splitting. The optimized electrocatalyst gives a current density of 10 mA cm−2 at an overpotential of 270 and 190 mV for the oxygen evolution reaction and hydrogen evolution reaction, and 1.57 V for total water splitting.