APPLIED SURFACE SCIENCE
·
2025
·
IF 6.9
Xinyao Li,Xiufang Cui,Yajie Guan,Di Chen,Guo Jin
To combat synergistic high-temperature wear-oxidation failure in critical components (e.g., gas turbines), this study designs laser-clad FeCoCrNi-Nb gradient high-entropy alloy coatings (Nb-GHEA). The monolithic gradient architecture integrating a Laves-phase-dominated surface, nanoscale eutectic transition, and ductile FCC substrate. The coating achieves oxidation resistance at 800 °C (mass gain: 0.056 mg·cm −2 ), attributed to sluggish diffusion forming an adherent Cr 2 O 3 -NbO 2 scale and dynamic Nb 4+ /Nb 5+ redox-mediated crack healing. Furthermore, it exhibits an ultra-low wear rate (9.29 × 10 −7 mm 3 ·N −1 ·m −1 ), friction coefficient (0.2207), and impact toughness (115.8 J) at this temperature. These enhancements primarily originate from multi-layer structure synergy, which transitions the dominant wear mechanism from adhesion to mild abrasion. This work establishes Nb-GHEA as a solution for critical tribological components under extreme conditions
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DOI
高影响因子
Journal of Materials Chemistry B
·
2019
·Vol. 7
·期 44
·7042-7051
·
IF 5.047
Lianjing Zhao,Zepei Wu,Guannan Liu,Huiying Lu,Yuan Gao,Fangmeng Liu,Chenguang Wang,Jiuwei Cui,Geyu Lu
Nanozymes have drawn considerable attention because of their lower cost, higher stability and convenient preparation compared to protein enzymes. In the present work, Mo, S co-doped carbon quantum dots (Mo-CQDs) as a peroxidase mimic were used to fabricate a cascade colorimetric biosensor to detect cholesterol. The Mo-CQDs possess a robust peroxidase-like activity, and they can easily catalyze 3,3,5,5-tetramethylbenzidine (TMB) to produce an oxidized TMB in the presence of H2O2. The Mo, S doping in the carbon quantum dots (CQDs) notably boosts the yield of CQDs and may facilitate the electron transfer between TMB and H2O2, which further enhances the catalytic activity of CQDs. The colorimetric biosensor based on Mo-CQDs and cholesterol oxidase exhibited excellent selectivity and high sensitivity for cholesterol in the range of 0.01–1.0 mM along with a detection limit as low as 7 μM. The total cholesterol concentration in the serum sample was measured with satisfactory results and read out by the naked eye, indicating the potential application in clinical diagnosis and portable test kits.
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PubMed
高影响因子
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
·
2022
·
IF 4.326
Xiaoxian Li,Yuanzhe Gong,Qi Lu,Min Lin,Jian Liu,Yulong Wu
In this work, the hierarchical pore HZSM-5 zeolite was synthesized by the method of alkali treatment, and the bimetallic loading of Mo and Cu was investigated for the hydrothermal aromatization of stearic acid. After alkali treatment, the pore size of HZSM-5 increased, but the acid sites decreased. The metal loading reintroduced the Lewis acid sites, greatly increasing the ratio to Brönsted acid sites. Therefore, the treated catalyst achieved higher hydrothermal stability while maintaining the high activity of hydrothermal aromatization of stearic acid. Mo0.02Cu0.01/Z-0.2M achieved excellent activity in the stearic acid hydrothermal aromatization with a high overall TEX (toluene, ethylbenzene, and xylenes) yield of 50.19 wt %, including 10.30 wt % toluene, 3.82 wt % ethylbenzene, and 36.07 wt % xylene. In addition, Mo0.02Cu0.01/Z-0.2M still showed excellent catalytic activity while applied in the system of the simulated microalgal bio-oil. As the reactant changed to the mixture of stearic acid and hexadecanamide, an overall TEX yield of 34.11 wt % was obtained at 450 °C. These results demonstrate the excellent hydrothermal aromatization ability of the MoCu-supported hierarchical pore ZSM-5 zeolite, which provides the potential to produce value-added chemicals from algal biomass.
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高影响因子
CERAMICS INTERNATIONAL
·
2026
·
IF 6
Tao Wang,Jian Zou,Jun Yang
A series of molybdenum (Mo) and cerium (Ce) co-doped Y 2 Zr 2 O 7 inorganic cool pigments were synthesized via a high-temperature solid-state reaction method. Substitution of Zr by Mo introduces interstitial oxygen into the lattice, leading to lattice expansion while enhancing the near-infrared reflectance of the pigments. Mo coexists in the form of Mo 6+ and Mo 5+ ions, with the yellow coloration primarily originating from Mo 5+ . The lattice expansion induced by the incorporation of larger Ce ions suppresses the formation of interstitial oxygen, thereby promoting an increase in Mo 5+ content, which results in a higher b* value while maintaining high near-infrared reflectance. The optimized composition (Y 1.55 Ce 0.45 Zr 1 Ce 0.65 Mo 0.35 O 7 ) exhibits the following chromatic parameters: L* = 88.26, a* = -3.19, b* = 55.15, and R NIR =93.68%. Furthermore, the simulation experiment revealed that the surface temperature of the coating based on the as-prepared pigment is 16.3 °C lower than that of the cement coating and 11.4 °C lower than that of the commercial iron yellow coating, demonstrating excellent solar reflective performance.
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高影响因子
Journal of Materials Chemistry A
·
2026
·
IF 9.2
Hamza M. Haruna,Yanxiang He,Zhixiao Zhu,Hao Yang,Selvam Mathi,Guanhua Zhang,Zhongmin Wang,M. Sadeeq Balogun
Controlling phase evolution during nitridation is essential for creating active interfaces in multi-metal electrocatalysts. However, the nitridation pathways in complex systems such as Mo-Fe-Ni molybdates remain poorly defined. Herein, tuning the Fe contents in the Fe-Mo precursor directly governs ammonia activation and drives nitridation-induced reconstruction. Increasing Fe concentration promotes NH3 decomposition, shifting the product from an oxide-rich phase (N-doped MoO2-FeMoO4-NiMoO4-NiO, denoted N/MoO2-MoFeNi-O) to a nitride-dominated heterostructure comprising MoO2, Mo2N, FeN and Ni4N (N/MoO2-MoFeNi-N). The optmized N/MoO2-MoFeNi-N nitride-oxide interfaces enhance electrical conductivity, optimize oxygen-intermediate adsorption, and improve corrosion resistance. As a result, N/MoO2-MoFeNi-N exhibits superior oxygen evolution performance in both alkaline freshwater and seawater, requiring overpotentials of only 309/392 and 334/499 mV to reach 500 and 1000 mA cm-2, respectively. DFT calculations identify the MoO2@FeN interface is the most active site with the lowest energetic barrier for the potential-limiting step. The catalyst also demonstrates efficient oxygen reduction activity, enabling high-performance zinc-air batteries with open-circuit voltage of 1.33 V, peak power density of 84.2 mW cm-2, and stable cycling over 140 h. This work clarifies the role of Fe in directing nitridation pathways, providing a rational route to construct durable, interface-rich nitride-oxide architectures for advanced oxygen atalysis.
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产品关联
DOI
高影响因子
TOPICS IN CATALYSIS
·
2026
·
IF 3.7
Wu Jundao,Huang Zeai,Zhang Fan,Liu Jiayi,He Yi,Hu Wei,Tang Xiao,Zairov Rustem,Sinyashin Oleg G.
The substantial presence of nitrogen oxides (NO and NO 2 ) in outdoor environments detrimentally impacts natural ecosystems and exerts significant influence on urban climates. Conventional NO x treatment methods frequently suffer from challenges such as harsh reaction conditions and high energy consumption. Consequently, the development of advanced photocatalytic systems to efficiently degrade NO x while minimizing the formation of toxic byproducts represents a critical challenge in environmental catalysis. In this study, a novel ternary composite material (5% Mo-CN/InP-NBOC) was constructed via hydrothermal synthesis and surface modification strategies, achieving 42% NO oxidation efficiency under visible light irradiation with a mere 0.9% NO 2 generation rate. This performance demonstrates efficient photocatalytic NO oxidation while effectively suppressing NO 2 production. Systematic characterization techniques, including XRD, TEM, and XPS, confirmed the successful integration of InP quantum dots (5–10 nm) and amorphous Mo-CN onto NBOC nanosheets, forming an intimate heterojunction structure. PL and ESR analyses revealed that Mo-CN enhances charge carrier separation and governs the NO oxidation process through the activation of dual free radical pathways (⋅O 2 − and ⋅OH). This work establishes a “quantum dot-primary catalyst-cocatalyst” ternary collaborative design paradigm, providing experimental evidence and theoretical models to address the challenges of synergistic optimization among activity, selectivity, and stability in photocatalytic NO x treatment.
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高影响因子
CARBON
·
2026
·
IF 12.7
Jia-yuan Tian,Feng Lin,Jing-jing Wu,Pei Ma,Xiao-lin Xue,Yu-long Ma,Yong-gang Sun
Lignin is the most abundant renewable organic aromatic compound carbon source in nature, and it is of great significance to convert it into high-value fine chemicals. However, achieving this goal requires regulating the selectivity of the lignin hydrodeoxygenation (HDO) reaction is crucial to breaking the competitive relationship between C–O bond cleavage and aromatic ring saturation. This study proposes oxygen-philic-hydrogen activation dual-functional site synergy strategy, using NiCoAl-LDH as the precursor, and constructing a NiCoMoFeAlO x multi-metal oxide catalyst by introducing Mo and Fe. Experiments and DFT calculations show that the catalyst achieves precise coupling of depolymerization and deoxygenation through a tandem synergy mechanism, the NiCo sites efficiently activate H 2 to supply active hydrogen, the oxygen-philic Mo sites and Fe selectively adsorb and cleave C–O bonds, and the intermetallic synergy effectively inhibits excessive hydrogenation of aromatic rings, directing the reaction path to phenolic products with retained aromatic rings. In the real lignin HDO reaction, the catalyst achieves a liquid yield as high as 78% and 64.9% selectivity for C 6+ cyclohexanol. This research provides a new paradigm for the rational design of multi-functional catalysts and the realization of directed conversion of lignin. Download: Download high-res image (244KB) Download: Download full-size image
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产品关联
DOI
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2025
·
IF 6.3
Rui Ming,JingJing Du,Shaobo Ye,Zhao Liang,Qiao Liu,Xuyang Lu,Qiliang Wei,Weiyou Yang,Qing Shi
The design of efficient and cost-effective bifunctional catalysts to replace precious metal-based catalysts remains a critical challenge in electrocatalytic water splitting. Herein, we report a Mo-Fe co-doped Ni 3 S 2 nanorod arrays grown on a nickel-iron foam substrate via a facile hydrothermal synthesis. This dual metal-doped nanorod structure synergistically modulates the electronic structure while maximizing accessible active sites, endowing the Mo-Fe-Ni 3 S 2 electrode with exceptional bifunctional activity for the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) in alkaline media. The resulting Mo-Fe-Ni 3 S 2 electrode requires only 180 mV for HER and 275 mV for OER at a current density of 100 mA cm −2 , coupled with long-term stability exceeding 50 h. Remarkably, when integrated into a single-stack cell for practical application, the Mo-Fe-Ni 3 S 2 electrode exhibits outstanding performance, achieving a current density of 100 mA cm −2 at a potential of 1.87 V and showing no potential degradation after 100 hours of continuous operation at 100 mA cm −2 . This work not only presents a high-performance bifunctional catalyst but also provides fundamental insights into the design of advanced electrocatalysts through rational heteroatom doping strategies.
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产品关联
DOI
高影响因子
JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY
·
2021
·
IF 8.067
Weiqiang Hu,Tao Sun,Chenxi Liu,Liming Yu,Tansir Ahamad,Zongqing Ma
The ultrafine Mo-Y 2 O 3 composite powders were successfully synthesized by innovative freeze-drying method. Consequently, the freeze-dried Mo-Y 2 O 3 composite powders with high sintering activities possess an average grain size of 54 nm. After low temperature sintering at 1600 °C, the Mo-Y 2 O 3 alloys maintaining a high density (99.6 %) have the finest grain size (620 nm) comparing with available literature about oxide dispersion strengthened molybdenum alloy (ODS-Mo). The oxide particles remain their small size (mainly <50 nm) within Mo grains and at Mo grain boundaries. Furthermore, the Y 5 Mo 2 O 12 particles were firstly observed within Mo matrix, and its formation can absorb nearby oxygen impurities, which involves the purification of Mo matrix. The mechanical properties show that Mo-Y 2 O 3 alloy possess a high hardness of 487 ± 28 HV 0.2 , a high yield strength of 902 MPa, a high compressive strength of 1110 MPa, respectively. Our work suggests that freeze-drying and subsequent low temperature sintering can shed light on the preparation of ultrafine ODS-Mo alloys with high performance.
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高影响因子
Journal of Materials Research and Technology-JMR&T
·
2024
·
IF 6.2
Xinyue Mao,Qingnan Meng,Sifan Wang,Shiyin Huang,Mu Yuan,Yuting Qiu
To effectively inhibit the thermal oxidation and thermal failure of diamonds when working in a high–temperature aerobic environment, a Mo–B–C coating was designed and prepared to protect diamonds from oxidation. A two–step synthesis method was used to form coatings with different B contents on diamonds by adjusting the reaction temperature, and the oxidation kinetics and oxidation mechanism of the coated diamonds were investigated in the temperature range of 700°C–1200 °C. The mechanism of diamond protection in this study was the preferential oxidative sacrifice of Mo–B–C coatings to form a stable oxide layer on the diamond surface. For low–B coatings, the four stages of coating oxidation, low-temperature volatilization of MoO 3 , stable protection by B 2 O 3 , and rapid evaporation of B 2 O 3 were experienced sequentially with an increase in temperature. For high–B coatings, the preferential self-healing flow of B 2 O 3 not only inhibited the volatilization of MoO 3 but also provided a reducing environment for MoO 3 to generate high melting–point MoO 2 and Mo 2 C, which resulted in the formation of a double synergistic protective oxide layer and greatly enhanced the oxidation resistance of diamonds. Meanwhile, the protection of the oxide layer also maintained the compressive strength of diamonds under a high–temperature oxidizing atmosphere, indicating its excellent high temperature applicability. This study provides an effective method for enhancing the high–temperature oxidation resistance and strength of diamonds, which can be effectively applied to the extreme environmental use of diamond tools.
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高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2022
·
IF 6.371
Jiaqi Wang,Guoxiang Wang,Li Cui,Dazhi Wang,Shiping Gao,Suhua Liu,Sa Liu,Hongfeng Xu
Bimetallic metal-organic framework (MOF) has attracted great interest as an electrode for supercapacitors . Most metal sources are limited to valences of + 2 and + 3. We select metal sources of Co (II) and Mo (VI) and demonstrated a crystalline bimetallic MOF precursor prepared by using a facile chemical synthesis. The one-step solvothermal strategy is assisted by thioacetamide (TAA) for the self-assembly Co-Mo-S nanosheet arrays (Co-Mo-S NSAs). TAA-induced etching is essential to regulate the assembly of amorphous structures. Otherwise, only a single-structure crystalline Co-Mo-S could be obtained. The Co-Mo-S NSAs show a large specific capacitance of 1805.28 F g −1 at a current density of 0.5 A g −1 . A Co-Mo-S NSAs//AC battery−supercapacitor hybrid (BSH) make with activated carbon as the negative electrode and Co-Mo-S NSAs as the positive electrode. At a current density of 0.5 A g −1 , the BSH shows a high energy density of 169.73 Wh kg −1 and a power density of 371.44 W kg −1 . After 50,000 cycles, the capacitance retention rate is as high as 94.44%, showing good reversibility and cycle life. This work provides an effective strategy for manufacturing bimetallic MOF-based metal sulfide heterostructure electrode materials for practical energy storage and conversion .
研究领域:
材料科学
·
能量存储与转换
·
电化学
·
纳米材料
·
超级电容器
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DOI
高影响因子
CHEMISTRY-A EUROPEAN JOURNAL
·
2017
·Vol. 23
·期 19
·4644-4650
·
IF 5.317
Lianshan Sun,Chunli Wang,Qujiang Sun,Yong Cheng,Limin Wang
With the aim of finding efficient non-noble metal catalysts for water splitting, hierarchical Ni-Mo-polydopamine microflowers (Ni-Mo 2 C/C MF) were synthesized through a facile aqueous-phase reaction at room temperature. NiMoO 4 nanowires were utilized as both Ni and Mo source; they can complex with dopamine to form a hierarchical structure and affect the scale of the final product. The energy dispersive spectroscopy (EDS) measurement of Ni-Mo 2 C/C microflowers (MF) shows a high content of Mo 2 C and Ni (>90 wt %). For the hydrogen evolution reaction (HER), the Ni-Mo 2 C/C MF displays a low overpotential of 99 mV at a current density of −10 mA cm −2 and a small Tafel slope of 73 mV dec −1 in 1.0 m KOH. By comparison with Mo 2 C/C microspheres (MS), the nanosized Ni-doped particles offer more active sites and enhance the kinetic performance. This facile synthesis strategy is also suitable for preparing other metal-Mo 2 C/C composites that can be used in the fields of catalysis and energy conversion. Graphical In flower : A flowerlike Ni-Mo-dopamine complex is first synthesized by a facile method under room temperature. Ni doping in situ is realized by utilizing NiMoO 4 nanowire as both template and precursor. An enlarged surface area and nanosized Ni doping greatly enhance the electrocatalytic properties of Ni-Mo 2 C/C due to more active sites.
研究领域:
材料科学
·
电化学
·
能量转换
·
纳米材料
·
催化
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高影响因子
危险品化学品经营许可证（带存储）