ACS Applied Materials & Interfaces
·
2024
·
IF 8.3
Guangyao Yang,Weiliang Peng,Zhipeng Chen,Shaobo Li,Qiying Han,Renzong Hu,Bin Yuan
Nickel–molybdenum–boron (Ni–Mo–B)-based catalysts with biphasic interfaces are highly advantageous in bifunctional electrocatalytic activity in alkaline water-splitting. However, it remains an ongoing challenge to obtain porous Ni–Mo alloy substrates that provide stable adhesion to catalysts, ensuring the long-term performance of bifunctional self-supporting electrodes at a high current density. Herein, a porous Ni–Mo alloy substrate was effectively obtained by a cost-effective dealloying process on a commercial Ni–Mo alloy with high-energy crystal planes. Subsequently, the Mo2NiB2/Ni3B bifunctional catalyst was in situ synthesized on this substrate via boriding heat treatment, resulting in outstanding catalytic activity and stability. Density functional theory (DFT) calculations reveal that the abundant biphasic interfaces and surface-reconstructed sites of the Mo2NiB2/Ni3B catalyst can decrease the energy barriers for the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), respectively. Thus, the designed self-supporting electrodes show bifunctional catalytic activity with overpotentials of 151 mV for HER and 260 mV for OER at a current density of 10 mA cm–2. Markedly, the assembled water electrolyzer can be driven up to 10 mA cm–2 at 1.64 V and maintain catalytic activity at a high current density of 1000 mA cm–2 for 100 h. The new strategy is expected to provide a low-cost scheme for designing self-supporting bifunctional electrodes with high activity and excellent stability and contribute to the development of hydrogen energy technology.
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RSC Advances
·
2024
·Vol. 14
·期 51
·38002-38008
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IF 3.9
Xin Li,Mohan Zu,Linzhuo Yan,Qiang Zhao,Liu Liu
A novel Mo–Fe bimetallic metal–organic framework [Fe2(4,4′-bipy)Mo2O8]·2H2O (1) was synthesized and characterized by X-ray single crystal diffraction, infrared spectroscopy (IR), thermogravimetric analysis (TGA), ultraviolet-visible spectroscopy (UV-vis), and its magnetic properties were studied. The compound demonstrates insolubility in most solvents and exhibits significant chemical stability across a wide pH range. Typically, exceptional selectivity and efficient conversion of sulfides to sulfoxides using 1 with H2O2 have been verified under ambient conditions.
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CHINESE JOURNAL OF CATALYSIS
·
2025
·
IF 17.7
Zhouzhou Wang,Qiancheng Zhou,Li Luo,Yaran Shi,Haoran Li,Chunchun Wang,Kesheng Lin,Chengsi Wang,Libing Zhu,Linyun Han,Zhuo Xing,Ying Yu
Neutral oxygen evolution reaction (OER) is a crucial half-reaction for electrocatalytic chemical production under mild condition, but with limited development due to low activity and poor stability. Herein, a tungsten-doped cobalt molybdate (WDCMO) catalyst was synthesized for efficient and durable OER under neutral electrolyte. It is demonstrated that catalyst reconstruction is suppressed by W doping, which stabilizes the Co-O-Mo point-to-point connection in CoMoO 4 architecture and stimulates to a lower valence state of active sites over the surface phase. Thereby, the surface structure maintains to avoid compound dissolution caused by over-oxidation during OER. Meanwhile, the WDCMO catalyst promotes charge transfer and optimizes *OH intermediate adsorption, which improves reaction kinetics and intrinsic activity. Consequently, the WDCMO electrode exhibits an overpotential of 302 mV at 10 mA cm –2 in neutral electrolyte with an improvement of 182 mV compared with CoMoO 4 electrode. Furthermore, W doping significantly improves the electrode stability from 50 h to more than 320 h, with a suppressive potential attenuation from 2.82 to 0.29 mV h –1 . This work will shed new light on designing rational electrocatalysts for neutral OER.
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2023
·
IF 9.9
Huizhen Wang,Pengfei Yang,Dongzheng Liu,Mengzhen Yu,Bowen Zhou,Yubing Zhang,Zhenyu Xiao,Weiping Xiao,Zexing Wu,Lei Wang
Developing efficient electrocatalysts for hydrogen evolution reaction (HER) in full pH range can promote the practical applications of hydrogen energy. In this work, nitrogen doped carbon nanosheets supported RuM (Mo, W, Cr) (RuM/NCN) are prepared through an ultrafast microwave approach. The carbon nanosheet structure coupled with the ultrasmall RuM nanoparticles can expose rich active sites to optimize the catalytic activity. Moreover, the strong metal-support interactions also favor to accelerate the reactions kinetics and improve stability. Thus, the developed RuMo/NCN (RuW/NCN) show excellent HER catalytic activities with overpotentials of 72 (75) mV, 82 (82) mV and 124 (1 1 9) mV to reach current density of 10 mA cm -2 in 1 M KOH, 0.5 M H 2 SO 4 and alkaline seawater , respectively, and also achieve excellent performance in 1 M PBS. This work provides a valid and novel avenue to design efficient electrocatalysts in renewable energy-related fields.
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APPLIED CATALYSIS B-ENVIRONMENTAL
·
2023
·
IF 22.1
Yingxue Du,Qichang Li,Linping Han,Pengfei Yang,Liantao Xin,Wei Jin,Weiping Xiao,Zhenjiang Li,Jinsong Wang,Zexing Wu,Lei Wang
Designing efficient and robust pH-universal electrocatalysts for hydrogen evolution reaction (HER) is the key to boost the development of eco-friendly hydrogen energy. Herein, metallic Mo, Ru coupled with graphitic carbon dots (GQDs) activate inertness 1D copper-based nanowires (GQDs@ Ru, Mo-Cu 2 O/CF) by surface chemical oxidation, solvothermal and low temperature calcination . The metals of Mo, Ru favor the water-dissociation and optimize the hydrogen adsorption/desorption. In addition, GQDs owns edge effect and good conductivity, and then benefiting electron transport and active sites exposure. Therefore, the synthesized GQDs@ Ru, Mo-Cu 2 O/CF requires only 30, 39, 17 and 55 mV in alkaline, acidic, alkaline seawater and neutral to achieve 10 mA cm −2 . Moreover, the assembled electrolyzer requires 1.58 V to reach 10 mA cm −2 in alkaline seawater, and maintained well at 200 mA cm −2 for 100 h. This research opens a new avenue for designing efficient catalysts on energy-relation applications through introducing both metal and non-metal.
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CHINESE JOURNAL OF CHEMICAL ENGINEERING
·
2026
·
IF 3.5
Pengfei Tian,Yunan Shen,Yuzhe Hua,Xiyu Zou,Guangmin Ren,Qingjie Guo,Hongjing Tian
Mo vacancy (V Mo ) and Se vacancy (V Se ) are doped into Bi 2 MoO 6 (BMO) and ZnSe, respectively, while they are mechanically ground and mixed to fabricate the dual S-scheme heterojunction. The lattice distortion is observed at the interface between V Mo -BMO and V Se -ZnSe/CdSe (V Se -ZCS) while XPS results confirm the construction of the dual S-scheme heterojunction V Mo -BMO/V Se -ZCS (V Mo+Se -BZCS). DFT simulation demonstrate that the doping of V Mo and V Se lead to more electrons transferring spontaneously through the heterojunction interfaces and promote the IEF strength accordingly. Both in-situ XPS and fs-TAS characterization prove the presence of a fast photoinduced charge transfer pathway from V Mo -BMO to V Se -ZnSe under LED light irradiation. V Mo and V Se function as the holes trapping center in V Mo -BMO and the electron trapping center in V Se -ZCS, respectively, thereby effectively suppressing the electron-hole recombination, which enhances the redox capability of V Mo+Se -BZCS together with the fast charge transferring. During the photocatalytic degradation experiments for the wastewater containing both tetracycline (TC) and Cr(VI), both the TC and the Cr(VI) degradation efficiency of V Mo+Se -BZCS are competitive under either LED or xenon lamp irradiation in comparison with some reported catalysts. Dual doping of V Mo and V Se were testified to amplify the bi-directional promotion effects (BPEs) between TC and Cr(VI).
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MATERIALS CHEMISTRY AND PHYSICS
·
2026
·
IF 5.2
Xiangqian Ren,Lianyan Zhu,Bin Guo,Wenting Liu,Shuang Yu,Xingfu Zhou
Ti/TiO 2 NTs/SnO 2 –Sb–Mo anode was prepared by adding intermediate layers and elemental doping and GF/Cu–C 3 N 4 cathode was prepared by impregnation method. The electrode was characterized by SEM, XRD, LSV, CV, and EIS, which show that a more uniform and finer-grained surface structure with higher electrocatalytic activity can be prepared by doping and the addition of TiO 2 -NTs interlayer. In addition, the cathode demonstrate the successful loading of Cu–C 3 N 4 on graphite felts (GFs) by SEM and EDS. The electrochemical test shows the high electrochemical activity. The high activity of the two-electrode system was verified according to the hydroxyl radical test, and then the two electrodes were applied to the degradation of 50 mg/L methylene blue wastewater at the same time, and the results showed that the degradation rate was 98.09% in 20 min, and the COD removal was as high as 80.11%, which is 1.33 times and 2.83 times of the single-anode and single-cathode systems, respectively. In addition, the system could show excellent degradation performance in a wide pH range. At the same time, the energy consumption of the two-electrode system is only 110.9 KWh/Kg. Finally, after ten consecutive decolorization experiments, the decolorization rate of methylene blue and the removal rate of COD could still reach 90.5% and 68.7% in 20 min, which indicated that the dual-electrode system had excellent reusability. The study opens a door to the practical application of electrochemical treatment of wastewater.
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JOURNAL OF NANOBIOTECHNOLOGY
·
2026
·Vol. 24
·期 1
·914
·
IF 15
Li Chenhao,Zhang Chao,Zhang Chuanqi,Duan Shiyu,Zhang Jiali,Wang Hongyue
AKI-to-CKD progression is shaped by sustained tubular stress, ferroptosis-related iron imbalance, and oxidative injury. To target this process, we developed an MHY1485-loaded molybdenum oxide (MoOx) nanozyme coated with a pH-responsive phenylboronic acid-polyethylene glycol-phenylboronic acid (PBA-PEG-PBA) polymer (MHY@MO@PPP). We tested whether this platform could weaken the ferroptosis-associated injury loop and delay AKI-to-CKD transition through regulation of the Fe 2+ -mechanistic target of rapamycin complex 1 (mTORC1)-glutathione peroxidase 4 (GPX4) axis. Material properties were examined by dynamic light scattering (DLS), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and liquid chromatography-tandem mass spectrometry (LC-MS/MS). Biological activity was assessed in erastin-induced ferroptotic human renal proximal tubular epithelial (HK-2) cells and in a C57BL/6 mouse unilateral ischemia-reperfusion injury (UIRI) model. MHY@MO@PPP showed stimulus-responsive MHY1485 release under simulated lesion-like conditions, lowered reactive oxygen species (ROS), lipid peroxidation, and free Fe 2+ , restored mitochondrial function, and improved cell survival. Mechanistic assays showed increased p-mTOR and GPX4 expression with reduced autophagy-related stress, supporting attenuation of the ferroptosis-related feedback state. Proteomic analysis and functional intervention experiments further implicated the Fe 2+ -mTORC1-GPX4 axis in the protective response. In vivo, MHY@MO@PPP improved renal function and reduced renal tissue injury and fibrosis. These findings support a nanozyme-based strategy that combines catalytic redox regulation with pathway modulation to mitigate AKI-to-CKD progression. Graphical abstract
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JOURNAL OF ENVIRONMENTAL MANAGEMENT
·
2026
·
IF 9.2
Lu Zeng,Xuexia Guo,Jiahao Sun,Wenbin Huang,Huinan Zhao,Lingling Hu,Shuanghong Tian,Chun He
In Fenton-like processes, achieving rapid and efficient redox cycling of metal active centers remains a challenge. This study presents an innovative strategy that harnesses the mechanical energy of water flow to drive the redox cycling of metal active centers. Herein, Fe 3 O 4 /MoS 2 heterojunction with interfacial Mo-S-Fe bridge bonds was constructed via a one-step hydrothermal method. Under the stimulation induced by water-flow mechanical, the piezoelectric effect of MoS 2 generates charge carriers, which are rapidly directed to Fe active sites through the Mo-S-Fe bonds. This process significantly accelerates the Fe(III)/Fe(II) cycle and enhances H 2 O 2 activation, achieving 93.8% removal of sulfamethoxazole (SMX) within 60 min under water flow stimulation. The composite exhibits robust performance across a broad pH range (3.0-10.7) and in the presence of humic acid (HA) and coexisting anions, demonstrating its strong environmental adaptability. Spectroscopic evidence confirmed the formation of Mo-S-Fe bonds at the heterojunction interface. Mechanistic studies further revealed that the structure improves charge separation, promotes rapid electron transfer from MoS 2 to Fe sites, and strengthens H 2 O 2 adsorption, thereby synergistically boosting reactive oxygen species (ROSs) generation and the overall catalytic efficiency. This study proposes an innovative strategy that exploits mechanical forces generated by water flow to drive rapid redox cycling of active metal centers in Fenton-like reactions.
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2022
·
IF 5.518
Yongkun Lun,Shuting Hu,Fuming Chen,Qinyu He,Yinzhen Wang,Wei Li,Guannan He
In this work, an S-scheme heterojunction-structured composite, g-C 3 N 4 /Mo-doped WO 3 (mass ratio 100:5, labeled 5M15WOCN) together with pure WO 3 , g-C 3 N 4 , and Mo-doped WO 3 (labeled M15WO) was prepared. The as-prepared samples were characterized by XRD , UV–Vis DRS, SEM, TEM, ESR , EIS , PL and XPS . The photocatalytic properties were investigated by photodegrading methyl orange (MO). The following findings were obtained. The dopant Mo increased the amount of O v -s and produced W 5+ , along with prolonging the lifetime of photogenerated carriers, improving the transfer ability of carriers. The S-scheme heterojunction g-C 3 N 4 /M15WO drastically improved the photocatalytic properties, dominantly due to the synergetic effect of the O v -s, S-scheme mechanism and very negative CB potential. A new phenomenon is found in which W 6+ can combine with the net electrons coming from the side with a higher Fermi level in the heterojunction and form W 5+ , suggesting a good method for stabilizing the high valence state for the material by combining one with a lower Fermi level. This work also implies that, compared to the S-scheme, a more negative CB is much more beneficial for MO photodegradation .
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2023
·
IF 7.2
Xinkuai He,Zhousi Hu,Jingjing Yang,Ruqing Guo,Luye Wu
The co-deposition behavior of Co(II) and Mo(VI) in N,N-dimethylformamide and ethylene glycol system is observed. The result implies that Co–Mo co-deposition is typical induced deposition, while containing ordinary deposition process . Mo(VI) species in the system can suppress the reduction of Co(II) and its effect can be improved as the increase of Mo(VI) concentration, however, Co(II) species can promote the reduction of Mo(VI) and the effect can also be improved as the increase of Co(II) concentration. SEM micrographs indicate that all these films exhibit a fibrous surface morphology with a new fluffy microstructure. XRD pattern reveals that the Co–Mo film is a Mo solid solution in Co and its average size of crystalline grain is 9.5 nm. In addition, the electrocatalytic activity for hydrogen evolution reaction (HER) on these Co–Mo films is investigated. These results indicate that its electrocatalytic activity can be improved as Mo content increases from 1.02 to 2.84 wt% and the prepared Co–Mo film with 2.84 wt% Mo presents a high electrocatalytic activity and stability for HER with an overpotential of 81 mV at 10 mA cm −2 .
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APPLIED CATALYSIS A-GENERAL
·
2020
·
IF 5.006
Guangci Li,Yanpeng Li,Guannan Lin,Da Wang,Peng Guo,Xuebing Li,Keng H. Chung
Co-Mo sulfide catalysts with different particle size and structures were prepared in ethanol-water mixed solvent followed by a low-temperature sulfurization process, and were tested in dibenzothiophene hydrodesulfurization . The effects of the ethanol/water ratio on the particle size of precursors, active phase composition, active site number, morphology, and hydrodesulfurization activity of the final catalysts were investigated. The atomic ratio of Co/Mo and active phase morphology of catalysts closely relate to the dielectric constant of ethanol-water mixed solvent. Appropriate dielectric constant favors the formation of (Co)MoS 2 slabs with shorter length (∼ 5.0 nm) and higher stacking number (∼ 4.3 layers), resulting in more coordinatively unsaturated sites, especially in the corner sites. The catalytic activity not only depends on the active sites of CoMoS phase, but also on that of Co 9 S 8 and MoS 2 phases because of synergistic effect. For MoS 2 and CoMoS phases, the corner sites show higher direct desulfurization activity than the edge sites.
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