FUEL
·
2025
·
IF 7.5
Yun Huang,Peipei Zhao,Kai Cui,Junwen Chen,Peng Wu,Xiaohong Li
The catalytic conversion of biomass-derived furfural and its derivatives such as furfuryl alcohol (FFA) into high value-added chemicals has been the subject of considerable attention within the field of biomass refining. Nevertheless, the selective hydrogenolysis of FFA represents a significant challenge to obtain the goal product such as 1,2-pentanediol (1,2-PeD) or 1,5-pentanediol (1,5-PeD) with satisfactory yield, due to complicated network involved in the FFA hydrogenolysis. Hence, selectivity control is the key to the hydrogenolysis of FFA. In this work, a 45Ni-Pr (45 wt% Ni/PrO x ) catalyst prepared using a facile sol–gel method behaved very well in the hydrogenolysis of FFA, resulting in up to 86.3 % yield of 1,5-PeD under mild reaction conditions. Introduction of PrO x enhanced Ni dispersion and promoted intimate contact between Ni species and PrO x . This created weak and medium-strong basicity and oxygen vacancies on the catalyst surface, which facilitated the adsorption of FFA via the C-O-C bond on the furan ring and C-OH at the side chain. Moreover, the 45Ni-Pr catalyst had the balanced Ni 0 and Ni 2+ sites, which guarantee not only the saturation of the C=C bond on the furan ring in the presence of Ni 0 sites to yield the intermediate tetrahydrofurfuryl alcohol (THFA), but also the subsequent ring-opening hydrogenolysis of THFA at the Ni 0 -O V -Ni 2+ -PrO x interfacial sites to produce 1,5-PeD selectively. This work establishes a viable and environmental benign approach for producing 1,5-PeD from the bio-based furfural derivatives, as well as a reference for the selective ring-opening hydrogenolysis of furan compounds.
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DOI
高影响因子
APPLIED CATALYSIS A-GENERAL
·
2025
·
IF 4.8
Zhenwen Yang,Ziyi Shui,Ben Niu,Xiaoxiao Duan,Zheng Wei,Guoxia Jiang,Zhengping Hao
NH 3 decomposition is receiving increased attention for on-site CO x -free H 2 generation. Unfortunately, the harsh reaction conditions often cause sintering of active metals. Here we report a simple method to achieve well Ni dispersion by nano-structuring the BN support with La species. The surface reaction-induced LaBO 3 nano-islands on BN support have a strong affinity for Ni atoms, which can capture and confine Ni species to yield a large population of well dispersed Ni clusters and nanoparticles. The Ni species selectively anchored on LaBO 3 islands expose more active sites and boost desorption of N 2 and H 2 , exhibiting superior activity and stability for NH 3 decomposition. In addition, it is revealed that the Ni dispersion is sensitive to the change of the support surface structure. These findings highlight the important role of support structure in determining the nature of the metal phase and provide guidance for designing catalysts with controlled catalytic structure and reactivity.
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DOI
高影响因子
ACS Catalysis
·
2024
·
IF 11.3
Xing Li,Lei Xing,Guoxiong Zhan,Zhoulan Huang,Zhen Chen,Huazhen Chang,Junhua Li
Catalytic carbamate decomposition is a feasible option for reducing the heat duty of amine solvent regeneration during the chemisorption of CO2 capture; advanced material with excellent proton transfer and exchange performance is crucial to boost the decomposition kinetics in an alkaline environment. Here, we prepared magnetic heterostructure Ni/NiO nanocatalysts with tunable Ni(0) nanoparticles and NiO support. The heterointerface of the proposed materials creates abundant surface oxygen vacancies (OVs) and offers abundant reactive active sites ascribed to the special electron transfer scheme of Ni0–NiO. The generated surface hydroxyls and unsaturated coordinated Ni, respectively, provide transferable protons and electrons, involved in the deprotonation of RNH3+ and C–N break of RNHCOO–. Thus, the obtained nanomaterials achieved considerably improved CO2 desorption of up to 3 mmol/min for a CO2-saturated monoethanolamine solvent, representing a substantial (approximately 50%) increase over the catalyst-free case. The reinforcement mechanism of OV generation by the Ni/NiO heterostructure and the induced proton transfer were revealed through in situ spectroscopic measurement and theoretical calculations. The results verified that the OVs stimulate the production of surface hydroxyls and water-assisted proton hopping, providing an advantageous condition for carbamate decomposition.
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DOI
高影响因子
Journal of Materials Chemistry A
·
2025
·
IF 9.5
Qingyun Liu,Yi Wang,Tianzhao Hu,Shaorui Chen,Yaozu Wang,Hui Zhao,Wu Zhang,Zhigang Yuan,Yulian Wang,Zhenhua Sun,Feng Li
Achieving high energy density in aqueous asymmetric electrochemical capacitors hinges on the development of electrode materials that combine exceptional capacitance with superior conductivity. Despite its high theoretical capacitance, Ni(OH)2 is limited by low intrinsic conductivity, significantly limiting its performance. In this study, a Mn–Ni(OH)2@1T-MoS2 heterostructure was synthesized through a facile growth method, achieving significant electrochemical performance boost. The lattice matching at the heterointerface induces a controlled lattice expansion in Mn–Ni(OH)2, while the interfacial interactions promote electron transfer from Mn–Ni(OH)2 to 1T-MoS2. These synergistic effects enhance conductivity and active site utilization, addressing the core challenges of pristine Ni(OH)2. As a result, the heterostructure exhibits a high specific capacity of 244.2 mA h g−1 at 1 A g−1 and a rate capability of 51.4% at 12 A g−1. Moreover, the assembled asymmetric electrochemical capacitor delivers an energy density of 61.67 W h kg−1 at 600 W kg−1 and maintains 72.7% capacity retention after 10 000 cycles at 5 A g−1. This work not only highlights the critical role of heterointerfaces in enhanced electrochemical performance but also provides a robust strategy for designing high-performance energy storage systems.
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DOI
高影响因子
CERAMICS INTERNATIONAL
·
2019
·
IF 3.45
Kun Qian,Zhengjun Yao,Haiyan Lin,Jintang Zhou,Azhar Ali Haidry,Tongbaihui Qi,Wenjing Chen,Xinlu Guo
Nanocrystalline Ni–Zn ferrites with different neodymium contents (Ni 0.5 Zn 0.5 Nd x Fe 2-x O 4 ) were synthesized by sol-gel route combined with self-propagating combustion (SPC) method. The presence of surface functional groups, crystal structure and morphology of the samples were studied by FT-IR, XRD and SEM. The results show that the prepared samples are composed of spinel phase under the condition of low neodymium content, like the pure Ni–Zn ferrite. While neodymium oxide appears after the content of Nd 3+ exceeds a certain limit (x > 0.04) and there exist two phases in the ferrite. The results of vibrating sample magnetometer (VSM) and vector network analyzer (VNA) show that adjusting the content of Nd is significant in improving the dielectric properties and microwave absorption capacity of the materials, specifically at low frequencies. When x < 0.04, the enhancement of dielectric loss ability of spinel ferrites by doping Nd 3+ is the dominant factor affecting microwave absorption ability of samples. The secondary phase Nd 2 O 3 hardly appears under this condition, thus the weakening effect of Nd 3+ addition on magnetic loss ability is not obvious. When x = 0.04, the optimal absorption peak of the material reaches −20.8 dB at 4.4 GHz with a thickness of 8.5 mm and the effective absorption bandwidth (R L < −10 dB) was 3.2 GHz. On the contrary, when x > 0.04, the magnetic loss ability decreases rapidly (e.g., Ms decreases from 82.47 emu/g to 59.77 emu/g). Meanwhile, the dielectric loss increases slowly and the microwave absorption capacity decreases.
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DOI
高影响因子
FUEL
·
2014
·
IF 3.406
Shuai Liu,Wei Zhou,Tao Yu,Ruijie Chai,Liming Lu,Renhe Yin
Layered nanoporous Ti/TiO 2 /Ni–W–B electrode is prepared through electrochemical anodization and electrodeposition for electrocatalytic reduction of coal. Extensive characterizations of the layered nanoporous Ti/TiO 2 /Ni–W–B electrode have been performed using techniques including scanning electronic microscopy, X-ray diffraction, inductively coupled plasma, Brunauer–Emmett–Teller and linear sweep voltammetry. The results indicate that the electrode, which presents layered nanoporous surface network, exhibits high activity for the reduction of coal. In an organic electrolyte system, a liquefaction yield of 51.8% is obtained after electrolysis of coal on the prepared electrode for 24 h at −1.7 V. The electroreduction mechanism of coal is also investigated. IR and 1 H nuclear magnetic resonance results show that active hydrogen (H ∗ ) reacts with functional groups in the coal such as C O, C O and C C, leading to the reduction of unsaturated bonds and the breakage of bridge bonds and part of aromatic rings during the electroreduction of coal.
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DOI
高影响因子
ELECTROCHIMICA ACTA
·
2017
·
IF 4.798
Yaohua Yang,Kai Yan,Jingdong Zhang
A Ni(OH) 2 /TiO 2 photoanode possessing high photoelectrocatalytic activity toward glucose oxidation driven by visible light was fabricated. The results indicated that deposition of Ni(OH) 2 on TiO 2 film electrode could remarkably promote the catalytic oxidation of glucose under visible light illumination. By applying a low voltage, the Ni(OH) 2 /TiO 2 electrode showed a linear photoelectrochemical response to glucose in the concentration range from 0.5 μM to 20 μM. Furthermore, the high photoelectrocatalytic activity of Ni(OH) 2 /TiO 2 electrode toward glucose oxidation was utilized to construct a glucose-air photofuel cell, which generated electrical signal responding to glucose concentration from 5 μM to 100 μM, without using external electrical power supply. Thus, dual non-enzymatic glucose sensors based on photocatalytic oxidation of glucose on the Ni(OH) 2 /TiO 2 electrode under visible light illumination were demonstrated.
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DOI
高影响因子
NANOTECHNOLOGY
·
2023
·Vol. 34
·期 14
·145704
·
IF 3.5
Jin Tan,Ling Lan,Yan-ni Wu,Song-bai Qiu
The graphene-like wrapped Ni@C catalysts were facilely synthesized by a modified sol–gel method. Nickel nitrate and citric acid (CA) were adopted as the raw materials to form sol–gel mixture. Under the circumstances, the additive CA were employed not only as a complexing agent but also as a carbon source. It is found that the calcination temperature and the mole ratios between Ni and CA are the key factors affecting the physical property and the catalytic performance of catalysts in the conversion of nitroarenes into corresponding anilines. The results show that the Ni@C-500(1:1) catalyst exhibited the best performance in the hydrogenation of o-chloronitrobenzenes (o-CNB) to o-chloroanilines (o-CAN). The yield of o-CAN was achieved at 100% when o-CNB was completely converted at 40.0 °C under 2.0 MPa H2 for 2.0 h. Furthermore, the Ni@C-500(1:1) catalyst could be separated and recovered easily after reaction by an external magnetic field. The investigated results indicate that the Ni@C-500(1:1) catalyst remained higher activity after using twelve times. More importantly, this kind of catalyst is also active for the selective hydrogenation of other nitroarenes into the corresponding anilines. This new synthetic method may pave a way for producing low-cost Ni@C catalysts on a large scale, which is attractive for industrial anilines applications.
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DOI
高影响因子
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2021
·
IF 5.816
Senliang Xi,Xiaojun Wang,Kudzaishe Caren Tome,Tonghuan Zhang,Zongying Han,Meng Gao,Shixue Zhou,Hao Yu
The hydrogen storage performances of MgH 2 improved by the addition of Ni and SAPO-34 were studied in detail. The mixture of MgH 2 with Ni and SAPO-34 was a physical reaction as shown by the X-ray diffraction (XRD) results. The SAPO-34 and Ni were uniformly distributed on the surface of MgH 2 . The thermodynamic and kinetic properties of 90MgH 2 /5Ni/5SAPO-34 were investigated by differential scanning calorimetry (DSC) and pressure-composition-isothermal (PCI) methods. The results showed that the dehydrogenation activation energy of 90MgH 2 /5Ni/5SAPO-34 decreased by 64.3 kJ/mol compared with that of MgH 2 . In addition, the relationship between the value of dehydrogenation heat and hydrogen content was also investigated by in-situ calorimetry. The enthalpy value of each sample in the dehydrogenation processes were calculated by in-situ calorimetry measurement. The dehydrogenation enthalpies of as-milled MgH 2 and 90MgH 2 /5Ni/5SAPO-34 were 63.2 kJ/mol H 2 and 53.6 kJ/mol H 2 , respectively. Thus, the co-doping of Ni and SAPO-34 contributed significantly to decrease the thermodynamic stability and improve the hydrogen sorption kinetic properties of MgH 2 .
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DOI
高影响因子
JOURNAL OF SUPERCRITICAL FLUIDS
·
2020
·
IF 3.744
Jie Sun,Lujiang Xu,Guo-hua Dong,Sonil Nanda,Hu Li,Zhen Fang,Janusz A. Kozinski,Ajay K. Dalai
Nickel-based catalysts with different supports and cobalt loadings were synthesized for hydrothermal gasification of cellulose at 350 °C. The activity of Ni catalysts was found in the order of Al 2 O 3 > spent bleaching clay ash > SiO 2 with H 2 yield of 80.6%, 69.0% and 57.0%. When 6 wt. % Co was added, 10Ni-6Co/Al 2 O 3 showed the highest H 2 yield of 88.4% i.e., 1.44 times that without Co addition. Catalysts were characterized by NH 3 -TPD, TPR, XRD, BET and XPS, showing that Ni-Co alloy formation promoted H 2 production. Single-factor experiments were conducted to study variables in the presence of 10Ni-6Co/Al 2 O 3 with the selected conditions of 0.5 g biomass and 20 min at 350 °C (achieving 94.9% H 2 yield from cellulose) for gasification of rice straw, peanut shell and cotton straw with the increase in H 2 yield by 51.4, 76.0 and 67.8 times. Ni-Co/Al 2 O 3 catalysts enhanced hydrothermal gasification of actual agricultural residues.
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DOI
高影响因子
Advances in Applied Ceramics
·
2019
·
IF 1.429
Guangyuan Yang,Sanwen Peng,Zheming Li,Zhixiong Huang
Carbon fibres (CF) have been used in various fields because of their unique properties. However, the oxidation resistance ability of CF is not good enough. The paper discusses the issue of using composite plating method to deposit SiC–MoSi2–ZrO2 coating at the surface of CF. The plating factors, including nanoparticle concentration, plating bath temperature, current density, agitation rate and electroplating time, which affect the structure and performance of coating have been discussed. The energy dispersive spectrometer has been applied to test the mass fraction of nanoparticles in the coating. Also, the surface morphology of coated CF has been characterised by a scanning electron microscope and the antioxidation ability of each sample has been tested by the weight difference method. The results indicate that with the proper plating factors, the coating can improve the antioxidation performance of CF and its reinforced composites. The residual weight of coated CF is over 52% after 1400°C oxidation for 15 min.
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DOI
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2023
·
IF 9.9
Mengwei Han,Yuzhu Qian,Xinni Li,Nailiang Wang,Ting Song,Li Liu,Xianyou Wang,Xiongwei Wu,Man-Kay Law,Bei Long
Developing insertion-type anode is key to advancing “rocking chair” zinc-ion batteries, though there are few reported insertion-type anodes. Herein, the Bi 2 O 2 CO 3 is a high-potential anode, with a special layered structure. A one-step hydrothermal method was used to prepare Ni-doped Bi 2 O 2 CO 3 nanosheet , and also a free-standing electrode consisting of Ni-Bi 2 O 2 CO 3 and CNTs was designed. Both cross-linked CNTs conductive networks and Ni doping improve charge transfer. Ex situ tests (XRD, XPS, TEM, etc.) reveal the H + /Zn 2+ co-insertion mechanism of Bi 2 O 2 CO 3 and that Ni doping improves its electrochemical reversibility and structural stability. Therefore, this optimized electrode offers a high specific capacity of 159 mAh g −1 at 100 mA g −1 , a suitable average discharge voltage of ≈0.400 V, and a long-term cycling stability of 2200 cycles at 700 mA g −1 . Besides, the Ni-Bi 2 O 2 CO 3 //MnO 2 “rocking chair” zinc-ion battery (based on the total mass of cathode and anode) delivers a high capacity of ≈100 mAh g −1 at 50.0 mA g −1 . This work provides a reference for designing high-performance anode in zinc-ion batteries.
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DOI
高影响因子
危险品化学品经营许可证（带存储）