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FUEL · 2022 · IF 8.035

Rationally control the path of hydrodeoxygenation of palmitic acid over Ni/red-mud catalysts by surface decoration of oxophilic MoOx species

Qi Wang,Xingyong Li,Jinyi Duan,Jinlei Chen,Yueyuan Ye,Dechao Wang,Shuirong Li,Zhifeng Zheng

Red mud supported Ni (Ni/RM) catalysts have been explored to the hydrodeoxygenation (HDO) of palmitic acid, however, the decarbonylation (DCO)/decarboxylation (DCO 2 ) is dominant. Therefore, the modification the oxophilic nature of catalysts can significantly impact their path of HDO and selectivity to aim products. Herein, MoO x -decorated Ni-Mo/RM catalysts with a hierarchical flower-like micro/nanostructure were prepared and applied in the HDO of palmitic acid. The effect of MoO x addition was investigated to control the path of HDO, resulting in the changing of carbon number distribution of the product. Combined with several comprehensive structural characterizations and catalytic HDO test, it is shown that the surface defective MoO x species and FeO x species near the metallic sites could significantly facilitate the C-O bond weakening, generated more direct deoxygenation product (hexadecane). Whereas the excessive Mo loading leads to clear altering of surface chemistry (i.e., decrease of specific surface area, pore volume and Mo 0 species, increase of reduction temperature and CO 2 adsorption, uneven dispersion, and agglomeration of Ni species), resulting in the decrease of palmitic acid conversion. As the main oxide in RM, Fe 2 O 3 , Al 2 O 3 and SiO 2 were used as supports to load Ni-Mo bimetals respectively to explore the contribution of different components in RM to the distribution of hydrodeoxygenation products of palmitic acid.

研究领域: 催化化学 · 材料科学 · 能源化学
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APPLIED SURFACE SCIENCE · 2022 · IF 7.392

The construction of strongly coupled interface for highly efficient oxygen and hydrogen evolution reactions

ShiWen Luo,ChengWei Deng,Kan Zhang,Sheng Zhu,QunJie Xu,YuLin Min

Reasonable interface regulation is a promising way to obtain bifunctional or multi-functional catalysts as the heterogeneous interface generally offers unique electronic structures. Here, we design a strongly coupled interface structure in Ni 3 Mo 3 N/Mo 2 C coated with graphitized carbon (Ni 3 Mo 3 N/Mo 2 C@C) by using an in-situ growth strategy. The density functional theory calculation unveil that the heterointerface of Ni 3 Mo 3 N/Mo 2 C@C not only facilitates the charge transfer, but also regulates the adsorption free-energies of the reaction intermediates (*O, *OH, and *OOH), to achieve superior electrocatalytic performances for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). As bifunctional catalysts, the Ni 3 Mo 3 N/Mo 2 C@C exhibits high HER and OER activities, with 43 mV and 220 mV overpotentials at the current density of 10 mA cm −2 in 1 M KOH electrolyte, respectively, as well as outstanding catalytic durability. This interface coupling strategy may provide a useful path to promote the electrocatalytic activities for diverse reactions in the energy field.

研究领域: 材料科学 · 能源科学
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Nanoscience and Nanotechnology Letters · 2017 ·Vol. 9 ·期 9 ·1356-1362 · IF 1.889

Fabrication and Electrocatalytic Activity of Hierarchically Nanoporous Ti–SiO2/Ni–Mo Composite Electrode for Hydrogen Evolution

Xu Jianxiong,Xie Shaowen,Feng Yahui,Du Jingjing,Xu Lijian

TiO2 nanoparticles with average diameter of 510 nm were prepared by sol–gel surfactants, and the hierarchically nanoporous Ti–SiO2 particles were further prepared using in-situ method. The hierarchically nanoporous Ti–SiO2 particles with hollow structure were analyzed by transmission electron microscope (TEM), energy dispersive spectrometer (EDS), scanning electron microscope (SEM), nitrogen adsorption stripping curves and Barrett-Joyner-Halenda (BJH) pore size distribution curves. Finally, the hierarchically nanoporous Ni–Mo composite electrodes were prepared using the TiO2 nanoparticles or nanoporous Ti–SiO2 particles as composite particles respectively, and the influence of the concentration of composite particles on the electrocatalytic activities of Ni–Mo composite electrodes for hydrogen evolution were investigated by polarization curves. The results showed that the diameter of Ti–SiO2 particles was from 200 nm to 500 nm, and specific surface area was 573 m2/g with pore volume of 1.19 cm3/g and mesopore size of 3.2 nm. The TiO2/Ni–Mo and Ti–SiO2/Ni–Mo composite electrodes were fabricated by electrodeposition with TiO2 nanoparticles and nanoporous Ti–SiO2 particles as composite particles respectively. The electrocatalytic activities of TiO2/Ni–Mo and Ti–SiO2/Ni–Mo composite electrodes for hydrogen evolution were investigated. Results showed that the electrocatalytic activities of TiO2/Ni–Mo and Ti–SiO2/Ni–Mo composite electrodes for hydrogen evolution reached the optimal value when the concentration of particles was 4 g/L and 2 g/L respectively. The electrocatalytic activities of TiO2/Ni–Mo and Ti–SiO2/Ni–Mo composite electrodes were greater than that of Ni–Mo alloy electrode, and the Ti–SiO2/Ni–Mo composite electrode showed the best electrocatalytic activity.

研究领域: 材料科学 · 电化学
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International Journal of Electrochemical Science · 2023 · IF 1.5

Ni-Mo Nanorod Bundles Grown within Nickel Foam for Excellent Electrochemical Performance

Jie Yuan,Hui Zhao,Ruizhuo Ouyang,Yuqing Miao

In this work, nanorod bundles of Ni-Mo-O were synthesized within nickel foam (NF) using a conventional hydrothermal method, which was the further vulcanized to form Ni-Mo-S upon doping sulfur. The NF/Ni-Mo-O and NF/Ni-Mo-S materials were characterized in terms of their morphology, composition and electrochemical properties. NF/Ni-Mo-O showed excellent performance as a supercapacitor. In addition, NF/Ni-Mo-S catalyzed the electrochemical oxidation of glucose in alkaline medium, exhibiting its potential application as a new fuel cell. Their excellent electrochemical performances greatly benefited from the preferred activity of NF/Ni-Mo-O and NF/Ni-Mo-S, efficient electron transfer over the electrode and high conductivity of NF.

研究领域: 材料科学 · 电化学
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JOURNAL OF MAGNETISM AND MAGNETIC MATERIALS · 2025 · IF 3

Improved properties of Fe-Ni-Mo soft magnetic composites via particle surface modification

Qi Li,Zhangqiao Zhou,Yan Nie,Lu Yang,Yu Wang,Jinsong Chen,Xian Wang

The preparation of soft magnetic composites requires effective surface modification of alloy powder to enhance insulating properties and achieve dense, uniform coating layers. Firstly, the gas-atomized Fe-Ni-Mo powder was surface modified using the atomic layer deposition method, forming a uniform and dense Al 2 O 3 insulating layer. The secondary surface modification of organic polymers further improves the properties of soft magnetic composites. This study systematically evaluates the effects of the primary and secondary surface modification on the properties of powder particles and soft magnetic composites. The primary modification generates an extremely thin insulating layer of approximately 2.5 nm, which increases the particle resistivity by 9 orders of magnitude. The permeability frequency stability of the soft magnetic composites increased from 11.3 % to 96.5 %, resulting in significant core loss reduction. The secondary modification effectively enhances the formability of soft magnetic composites. Optimal permeability of 242.7 at 1 kHz is achieved, maintaining 95.2 % frequency stability up to 1 MHz, while core loss remains below 570 mW cm −3 under 100 kHz/100 mT conditions. The surface treatment method in this work can provide a reference for the surface insulation modification of soft magnetic composites.

CAS / MDL: 67-64-1 75-24-1
研究领域: 材料科学 · 电磁学
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SURFACE & COATINGS TECHNOLOGY · 2023 · IF 5.4

The performance and corrosion resistance of an electrodeposited Ni-Mo-Cu HER catalyst

Jian Zhang,Hongxing Lu,Peng He,Zijie Ren,Guofang Shen,Ruxia Liu,Lei Wang,Guoqiang Luo

This study presents a facile electrodeposition and annealing procedure for the fabrication of Ni-Mo-Cu catalysts for hydrogen evolution reaction . Cu addition augmented the surface area and conductivity, while the synergistic effect of the three elements enhanced the intrinsic catalytic activity. After annealing in a vacuum at 300 °C, a dense Cu-Ni solid solution was formed on the catalyst surface, which improved the distribution of components and led to a significant improvement in corrosion resistance . Compared to the directly deposited Ni-Mo catalyst, the annealed Ni-Mo-Cu catalyst exhibited a reduced overpotential of 143 mV to generate a current density of 10 mA cm −2 in 1 M KOH at 25 °C, and its corrosion current density diminished from 0.21 to 0.035 mA cm −2 in 0.5 M NaCl at 25 °C.

CAS / MDL: 12054-85-2
研究领域: 材料科学 · 电化学
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2021 ·Vol. 32 ·期 11 ·14966-14975 · IF 2.478

Construction of Ni–Mo–P heterostructures with efficient hydrogen evolution performance under acidic condition

Chen Tian-Yun,Zhang Ya-Qi,Fu Ying-Yan,Qian Min,Dai Hao-Jiang,Ye Bo,Qin Shan,Yang Qing-Hua

Hydrogen energy is regarded as one of the most important clean energy in the twenty-first century, and improving the catalytic efficiency of hydrogen evolution reaction (HER) is the basis for realizing the large-scale hydrogen production. Transition metal phosphides (TMPs) were proved to be efficient electrocatalysts for HER. In this work, we first synthesized the nickel-molybdenum bimetallic precursors, followed by high-temperature calcination in air. Finally, NiMoP/MoP nanorods (Ni–Mo–P NRs) was obtained by chemical vapor deposition (CVD) of phosphating. The target catalyst of Ni–Mo–P NRs was characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). For Ni–Mo–P NRs, the electrochemical test in 0.5 M H 2 SO 4 solution for HER showed that the optimal feeding ratio was Ni:Mo = 1:1. And the Ni 1 –Mo 1 –P NRs presented an onset potential of 63.2 mV, and an overpotential of 117.9 mV was required to drive the current density of 10 mA cm −2 . Meanwhile, The Tafel slope, exchange current density ( j 0 ), electrochemical double-layer capacitance ( C dl ) were 58.6 mV dec −1 , 0.10 mA cm −2 , 12.6 mF cm −2 , respectively. Moreover, there was no obvious activity diminish of Ni 1 –Mo 1 –P NRs after a long-term stability and durability test.

研究领域: 材料科学 · 能源科学
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Energy Technology · 2023 ·Vol. 11 ·期 8 ·2300118 · IF 3.8

A Low-Cost Ni–Mo Electrocatalyst for Highly Efficient Hydrogen and Oxygen Evolution Reaction

Peiyao Pan,Qingle Zeng,Xiaoxiao Li,Chao Liu,Jinming Zeng,Tongxiang Liang,Xiaopeng Qi

Electrocatalytic water splitting provides an effective way to store electrical energy (i.e., solar and wind energy) intermittently. It is believed that developing electrocatalysts with excellent stability, high catalytic efficiency, and abundant natural reserves is the key to the industrialization of electrochemical water splitting. Herein, nickel–molybdenum electrocatalyst formed on the surface of a low-cost etched stainless-steel mesh via a one-step electrodeposition method exhibits a low hydrogen evolution overpotential of 53 mV and oxygen evolution overpotential of 261 mV at a current density of 10 mA cm −2 due to the synergistic effect of nickel and molybdenum. Moreover, the as-prepared catalyst demonstrates superior hydrogen evolution reaction (HER) catalytic performance than commercial Pt/C at current density exceed 200 mA cm −2 . The electrocatalyst also shows excellent HER and oxygen evolution reaction stabilities at high current density attribute to the tightly bond between electrocatalyst and the etched stainless-steel mesh, as well as the surface reconstruction of catalyst during the cycle test. The facile electrodeposition method has lower requirements on production equipment, using stainless steel mesh as the basement reduces the production cost, the nickel–molybdenum alloy possesses excellent electrolytic water splitting performance and stability. These results indicate that this work can provide an idea for the industrialization of electrochemical water splitting.

研究领域: 材料科学 · 能源化学
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Crystals · 2026 ·Vol. 16 ·期 1 ·51 · IF 2.4

Electrodeposition and Corrosion Resistance of Ni-Mo Alloy Coating: Effect of Electroplating Bath pH Values

Xi Shi,Shiyuan Zhu,Qiongyu Zhou,Bo Liang,Jun Li,Guangji Li,Longquan Chen,Peijun Xu

Ni-Mo alloy coating has shown exciting potential as a candidate to replace chromium coating. In this paper, Ni-Mo alloy coatings were successfully electrodeposited from a citrate/ammonia bath, and the effect of the bath pH values over a wide range (4–10) on the characteristics and corrosion resistance of Ni-Mo alloy coating was studied in detail. Results show that all the deposited Ni-Mo alloy coatings consist of a crystalline solid-solution Ni(Mo) fcc structure. An increase in bath pH values could facilitate the deposition of Mo, thereby increasing the Mo content and decreasing the crystallite size of Ni-Mo alloy coatings. However, there are subtle gaps between the coarse grains on the surface of the Ni-Mo alloy coating deposited at pH 10. These subtle gaps tend to form between the coarse grains on the surface of the electrodeposited Ni-Mo alloy coating because of the relatively high Mo content, refined grains, and appropriate morphology. The Ni-Mo alloy coating deposited at pH 9 exhibits optimal corrosion resistance, attributed to its lowest corrosion current densityicorr(7.31 × 10−6A cm−2), the strongest polarization resistance (11.13 kΩ·cm−2), and impedance value, which are mainly contributed to by the coating resistance and charge-transfer resistance.

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CATALYSIS LETTERS · 2017 ·Vol. 147 ·期 10 ·2515-2522 · IF 2.799

Controlled Synthesis of Mesoporous Nitrogen-Doped Carbon Supported Ni-Mo Sulfides for Hydrodesulfurization of Dibenzenethiophene

Zhang Zhenwei,Jiang Xingmao,Hu Jianheng,Yue Chuanjun,Zhang Jintao

Mesoporous nitrogen-doped carbon was synthesized in a controlled manner by a modified deep eutectic solvent method using silica nanoparticles as templates. Various amounts of urea and glucose, which contain hydrogen acceptor and hydrogen bond donor groups were heated and stirred to form homogeneous liquid precursors like deep eutectic solvents, and nitrogen element was uniformly dispersed on an atom scale. Ni-Mo sulfides supported on mesoporous carbon with varying N dopping exhibit excellent hydrodesulfurization (HDS) catalytic performance such as high conversion and good recycling stability in the HDS of dibenzenethiophene. Further investigation showed that a suitable N content in the carbon support enhance the HDS properties and the HDS conversion could reach up to 96%. Graphical

研究领域: 材料化学 · 催化化学 · 纳米材料 · 能源化学 · 环境催化
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INORGANIC CHEMISTRY · 2023 · IF 4.6

Bimetals Ni–Mo–S-Modified Hollow Cubic Cu2–xS for Visible-Light Photocatalytic H2 Evolution

Ning Li,Wenwen Zhao,Linping Li,Yangqin Gao,Lei Ge

Photocatalysts with hollow structures have drawn great interest owing to their high specific surface area, which can enhance the photocatalytic performance. Herein, we designed the hollow cubic Cu2–xS@Ni–Mo–S nanocomposites by vulcanizing from the Cu2O template and loading the Ni–Mo–S lamellas. The Cu2–xS@Ni–Mo–S composites greatly improved the photocatalytic hydrogen performance. Among them, Cu2–xS–NiMo-5 achieved the optimal photocatalytic rate of 1326.07 μmol/g h, which is approximately 3.85 times higher than that of hollow Cu2–xS (344 μmol/g h) and had good stability for 16 h. The enhanced photocatalytic property was attributed to the metallic behavior of bimetallic Ni–Mo–S lamellas and the LSPR (localized surface plasmon resonance) effect of Cu2–xS. The bimetallic Ni–Mo–S can effectively capture the photogenerated electrons and quickly transfer-diffuse to produce H2. Meanwhile, the hollow Cu2–xS not only provided many more active sites to take part in the reaction but also introduced the LSPR effect to increase the solar utilization. This work provides valuable insights into the synergistic effect of using non-precious metal co-catalysts and the LSPR materials to assist in the photocatalytic hydrogen evolution.

研究领域: 材料化学 · 光催化 · 能源科学 · 纳米材料 · 半导体物理 · 可再生能源 · 表面科学
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JOURNAL OF ALLOYS AND COMPOUNDS · 2015 · IF 2.999

Processing and microstructure characterization of SiCp/Hastelloy(Ni–Mo–Cr) composites prepared by pressureless infiltration

Qian Qi,Yan Liu,Hui Zhang,Yinsheng Li,Hanqin Liang,Zhengren Huang

SiC p /Hastelloy composites were fabricated by pressureless Ti-activated infiltration process. The wetting and infiltration behaviors of Hastelloy on the SiC substrates and the interfacial reaction between the SiC particles and Hastelloy were investigated by real-time observation system, X-ray diffraction (XRD) and scanning electron microscopy (SEM) equipped with energy X-ray dispersive spectroscopy (EDS) system. The results demonstrated that the Hastelloy had a good wettability on SiC ceramic and could spontaneously infiltrate into the Ti-activated SiC preform. Moreover, intensive interfacial reaction similar to SiC/Ni system was found between the SiC particles and Hastelloy, which induced defects in the microstructure. In order to inhibit the interfacial reaction, Al 2 O 3 coating on SiC particles was adopted as a diffusion barrier, which effectively reduced the extent of the interfacial reactions.

CAS / MDL: 7440-32-6
研究领域: 材料科学 · 冶金工程
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