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Reinforcing oxygen electrocatalytic activity via selective dualphase heterointerface engineering for rechargeable Zn-air batteries

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Rare Metals 2024年第4期43卷 1524-1536页

作者： Chao Cheng Chuang Zhi Zhong-Ti Sun Yong-Qiang Ming Ting-Ting Xiang Qing-Chao Zhu Zi-Rui Wu Bing Li Yi Li Cheng Jin Yong Cao Juan Yang School of materials science and engineering Jiangsu University Faculty of material science and engineering Kunming University of Science and Technology

Dual-phase heterointerface electrocatalysts（DPHE） constructed by oxygen reduction reaction（ORR）-and oxygen evolution reaction（OER）-active elements exhibit excellent bifunctional activity and long-term durability due to the abundant interface exposure and synergistic catalytic effect.Herein,low-dimensional N-doped graphene nanoribbons（N-GNRs） coupling with ultrathin CoO nanocomposites（N-GNRs/CoO） were controllably fabricated through a facile two-step approach using synthesized Co（OH）2nanosheet as CoO precursor.Density functional theory（DFT） calculations and experimental characterizations prove that the formation of interface between N-GNRs and CoO can induce local charge redistribution,contributing to the improvement of catalytic activity and stability.The optimal N-GNRs/CoO DPHE possesses hierarchically porous architectures and presents outstanding bifunctional activities with a small potential gap of 0.729 V between the potential at 10 mA·cm-2for OER and the halfwave potential for ORR,which outperforms Pt/C+IrO2and the majority of noble-metal-free bifunctional catalysts.Liquid-and solid-state rechargeable Zn-air batteries assembled with N-GNRs/CoO as the cathode also display high peak power density and fantastic cycle stability,superior to that of benchmark Pt/C +IrO2catalyst.It is anticipated to offer significant benefits toward high activity,stability and mechanical flexibility bifunctional oxygen electrocatalysts for rechargeable Zn-air batteries.

关键词： Interface engineering Graphene nanoribbons CoO Bifunctional electrocatalyst Zn–air batteries

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Microstructures and Properties of Biomedical Mg-Zn-Sn-Zr Rolled Alloys

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Journal of Wuhan University of Technology(materials science) 2024年第3期39卷 766-773页

作者：周生刚 ZHANG Daxin XU Yang DUAN Jihao LI Tao LIU Junfeng WANG Peng 曹勇 Faculty of material science and engineering Kunming University of Science and TechnologyKunming 650093China

The as-cast Mg-2.0Zn-1.5Sn-xZr(x=0,0.4,0.6,0.8,1.0 wt%)alloy was rolled with the pressure less than 5%each time.The microstructure,mechanical properties,corrosion properties and biocompatibility of the alloy were investigated.The microstructure of the alloy was observed and analyzed by scanning electron microscope,and the tensile test was carried out by universal tensile machine.The corrosion resistance of the alloy in Hank's solution was studied by hydrogen evolution experiment and electrochemical test,and the biocompatibility of the alloy was tested by L929 cells.The results show that Mg-2Zn-1.5Sn-xZr alloy has excellent mechanical properties.The elongation of Mg-2Zn-1.5Sn-xZr alloy decreases with the increase of Zr content,but the tensile strength first increases and then decreases with the increase of Zr concentration.When the Zr content is 0.8 wt%,the maximum tensile strength of the alloy is 235 MPa.The results of hydrogen evolution experiment and electrochemical analysis show that the corrosion resistance of the alloy is the best when the Zr content is 0.8 wt%,and all the five alloys have high biocompatibility.In conclusion,the rolled alloy has good properties and has broad application prospects in the field of biomaterials.

关键词： magnesium alloy corrosion performance mechanical properties biocompatibility

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Enhanced visible light absorption of Bi2WO6/SiO2 with abundant adsorbed oxygen for the degradation of organic pollutant

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Particuology 2024年第5期88卷 210-217页

作者： Yuanting Wu Xiaoying Wang Wenlong Zhong Shan Zhang School of material science and engineering Shaanxi University of Science and TechnologyXi'an 710021China

Heterogeneous photocatalysts exhibit high catalytic efficiency in the degradation of pollutants,but their stability and repeatability is not very good and requires high structural matching.Simply by nanosizing the pure Bi 2 WO6(BWO)photocatalyst without constructing a heterojunction,there is a significant improvement in its performance,with an enhancement effect of about 2.3 times(99.43%).The high photocatalytic degradation efficiency of the material can be attributed to the enhanced light absorption effect brought by the three-dimensional inverse-opal structure SiO 2(IS)and the abundant surface adsorbed oxygen generated after the formation of Si–O–W bonds.In addition,the introduction of IS greatly increases the surface area of nanostructured BWO,which accelerates the charge transfer process,while the adsorbed oxygen promotes the participation of·O2−in the photocatalytic reaction,thereby accelerating the consumption of photo-generated electrons and ultimately improving the separation of charge carriers.Furthermore,the matched photonic bandgap further improves the absorption and utilization of light of the material.In this work,we constructs Si–O–W bonds to obtain inverse-opal SiO2/Bi2 WO6 with uniformly growth of pure phase nano BWO,which provides a feasible strategy for the preparation of high-performance pure-phase photocatalysts.

关键词： Bi2WO6 SiO2 inverse-opal structure Photocatalysis Adsorbed oxygen

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Polyoxometalates-derived ternary metal oxides electrocatalyst for N_(2) reduction under ambient conditions

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Tungsten 2024年第2期6卷 428-437页

作者： Meng-Le Yang Zhong-Xin Jin Xi-Xian Cao Xin-Ming Wang Hui-Yuan Ma Hai-Jun Pang Gui-Xin Yang The School of material science and Chemical engineering Harbin University of Science and TechnologyHarbin 150040China

Accelerating the breaking of the nitrogen nonpolar bond(N≡N)is an important factor to improve the effi ciency of the electro-catalytic nitrogen reduction reaction(e-NRR).In this work,polyoxometalates-derived FeMo-based ternary oxide materials MoO_(2)-Mo_(4)O_(11)-FeMoO_(4)@X(abbreviated as MoFeO@X,X represents the synthesis temperature of 650,750 and 850℃)were designed and synthesized for e-NRR under ambient conditions.The scanning electron microscopy images of MoFeO@750 show an ellipsoidal-like structure(0.86×0.6μm).The relatively large specifi c surface area,formation of multiple interfaces,together with the synergistic eff ect of iron and molybdenum bimetals,would make MoFeO@X catalyst more easily absorb and activate N_(2)in the e-NRR.Expectedly,the synthesized MoFeO@750 shows an optimal NH_(3)production rate of 16.57μg·h^(−1)·mg cat.^(−1)and Faradaic effi ciency of 12.33%at−0.3 V versus reversible hydrogen electrode(νs.RHE),with outstanding electrochemical and structural stability.

关键词： Polyoxometalates Electrocatalytic nitrogen reduction reaction Ternary oxide Electrocatalyst

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PVP/PAN-derived porous carbon fiber for zinc-ion hybrid supercapacitors

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Rare Metals 2024年第7期43卷 3066-3073页

作者： Shu-Hua Yang Wen-Qing Fu Yan-Wei Cui Bing-Qiang Cao materials Center for Energy and Photoelectrochemical Conversion School of Material Science and EngineeringUniversity of Jinan

Porous carbon fibers are promising cathodes for zinc-ion hybrid supercapacitors（ZHSs） owing to their abundant active sites,great conductivity,and stable physical and chemical properties.However,designing a proper preparation technique to regulate the microstructure of carbon fibers still remains a great challenge.Here,a poly vinylpyrrolidone/po-lyacry lonitrile（PVP/PAN）-derived porous carbon fiber is developed via the PVP/PAN blend electrospinning and hydrothermal selective PVP removal strategy.The hydrothermal selective PVP removal strategy can effectively avoid a cross-linking between PVP and PAN during the traditional stabilization at air atmosphere.In PVP/PAN-derived porous carbon fiber,the sufficient micropores provide abundant space for the Zn2+storage,whereas the proper mesopores contribute to the fast ion transfer.These hierarchical porous structures endow ZHSs with high specific capacity and high-rate performance.The ZHS assembled with the optimal PVP/PAN-derived porous carbon fiber（PVP-PANC-0.8） displays an outstanding specific capacity of 208 mAh·g-1,high rate capability（49.5%） from 0.5 to 5 A·g-1,and 72.25% capacity retention after 10,000 cycles at 0.5 A·g-1.

关键词： Zinc-ion hybrid supercapacitors Porous carbon fibers Hierarchical porous structures Electrospinning

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Constructing core@shell structured photothermal nanosphere with thin carbon layer confined Co-Mn bimetals for pollutant degradation and solar interfacial water evaporation

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Rare Metals 2024年第4期43卷 1686-1701页

作者： Hong-Yang Zhu Meng-Ting Liu Gang Wang Rong-Rong Du Hong-Yao Zhao Hao Lu Shi-Qi Yang Sheng Tang Zeng-Jing Guo Jun Yang Cheng-Zhang Zhu Fu Yang School of Environmental and Chemical engineering Jiangsu University of Science and Technology School of Chemistry and Chemical engineering Liaocheng University School of material science and engineering Jiangsu University of Science and Technology School of Environmental science and engineering Nanjing Tech University

Photothermal material applied in environmental governance has attracted growing attention.By combining the Stober method and dopamine-triggered coating strategy,Co-Mn precursor was in situ incorporated into the poly dopamine（PDA） layer over the surface of silica cores.Afterwards,a unique photothermal nanosphere with SiO2core and thin carbon layer and dual Co-Mn oxides shell was allowed to form by sequential heat treatment in the inert atmosphere（SiO2@CoMn/C）.The bimetallic fraction of Co/Mn in the carbon layer and post-treatment calcination temperature was comprehensively tuned to optimize the peroxymonosulfate（PMS） activation performance of the catalyst.The state of bimetallic species was studied including their physical distribution,chemical valence,and interplay by various characterizations.Impressively,Co oxides appear as dominant monodispersed nanoparticles（～ 10 nm）,while Mn with cluster-like morphology is observed to uniformly distribute over thin-layer carbon and adhered to the surface of SiO2nanospheres（～ 250 nm）.The calcined temperature could tune the oxidized state of Co species,leading to the optimization of the catalytic performance of introduced dual metal species.As a result,this obtained optimal catalyst integrated the advantages of exposed bimetallic CoMn species and N-doped thin carbon to deliver excellent catalytic PMS activation performance and photothermal synergetic catalytic mineralization ability for diversiform pollutants.Further reactions condition controls and anion interference studies were conducted to identify the adaptability of the optimal catalyst.Moreover,the application of solar-driven interfacial water evaporation using optimal SiO2@Co3Mn1/C-600 catalyst was explored,showing a high water evaporation rate of 1.48 kg·m-2·h-1and an efficiency of 95.2%,further revealing a comprehensive governance functionality of obtained material in the complex pollution condition.

关键词： Photothermal Peroxymonosulfate (PMS) activation Bimetallic synergy Water evaporation Advanced oxidation process

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Coupling N-doping and confined Co3O4 on carbon nanotubes by polydopamine coating strategy for pleiotropic water purification

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Rare Metals 2024年第7期43卷 3146-3160页

作者： Wen-Long Tu Gang Wang Yue Zhang Hong-Yang Zhu Rong-Rong Du Hong-Yao Zhao Sheng Tang Zeng-Jing Guo Jun Yang Fu Yang Cheng-Zhang Zhu School of Environmental and Chemical engineering Jiangsu University of Science and Technology School of Chemistry and Chemical engineering Liaocheng University School of material science and engineering Jiangsu University of Science and Technology School of Environmental science and engineering Nanjing Tech University

The development of effective and sustainable solutions for pleiotropic water purification becomes urgent and attractive.Heterogeneous Fenton-like catalysts for activation of peroxymonosulfate（PMS） to purify organic wastewater show great promise.In this work,by tuning metal loading with an in-situ polydopamine coating strategy,oxygen vacancy-enriched Co3O4loading on N-doped carbon nanotubes（CNTs） were constructed to enhance PMS activation efficiency for pollutants degradation.Impressively,the obtained modified CNTs afford a well-developed N-containing network structure,which is further endowed with abundant Co（Ⅱ）/Co（Ⅲ） redox cycles and significant metal-carbon interactions.In particular,the surface N doping in CNTs might induce the oriented enrichment of pollutants around the catalyst,which reduces the migration distance and correspondingly improves the utilization of reactive oxidative species.The electron transfer efficiency of the catalyst can be further improved by incorporating oxygen vacancy-enriched Co3O4.The performance results show that the optimal NC/Co-1 could mineralize 20 × 10-6of bisphenol A（BPA） by almost 98% in 8 min.A low reaction activation energy(26.05 kJ·mol-1) in BPA degradation was demonstrated by the NC/Co-1.More importantly,NC/Co-1 can inherit excellent degradation performance towards oxytetracycline,2,4-dichlorophenol,and tetracycline,showing wide practical flexibility.In addition,by virtue of the photothermal conversion property,NC/Co-1 achieves an additive function for interfacial solar water evaporation(1.84 kg·m-2·h-1,112.51%),showing impressive potential for clean water recovery under complicated environmental pollution conditions.

关键词： Carbon nanotube Advanced oxidation process Co 3 O 4 Photothermal conversion Solar water evaporation

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Role of Crystal Seed in Aluminum Hydroxide Crystallization from Ammonia System with Added NH_(4)Al(SO_(4))_(2)·12H_(2)O

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Journal of Wuhan University of Technology(materials science) 2024年第4期39卷 945-953页

作者：王俊凯李来时 LIU Feng WANG Yuzheng 吴玉胜 School of material science and engineering Shenyang University of TechnologyShenyang 110870China

A method to promote aluminum hydroxide crystal growth through pickling Al(OH)_(3)as seed in the ammonia system was proposed to overcome these defects.The experimental results show that,under the conditions of pickling time of 15 min,the acid concentration of 10%,the addition of 70 g/L pickling-Al(OH)_(3)seed,and the coarse granular Al(OH)_(3)products(d0.5=85.667)can be obtained.The characterization results show that the phase of the product is gibbsite,consistent with the seed.Moreover,the steps and ledges can be formed on pickling Al(OH)_(3)seed surface under the ammonia system,effectively promoting crystal growth.During crystal growth,the roughness of the crystal surface was first increased and then decreased,and the lamellar structure was deposited on the crystal seed surface.The final particles are approximately round,the surface is compact and dense.The growth of the product is surface reaction controlled.In addition,the content of the AlO_(6)unit is increased and contributed to Al(OH)_(3)crystal growth.

关键词： reactive crystallization coarse-grained Al(OH)_(3) crystal seed crystal growth process

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High-current pulsed electron beam modification on microstructure and performance of Cu/CuW diffusion bonding joints

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Rare Metals 2024年第6期43卷 2819-2831页

作者： Na-Na Tian Cong-Lin Zhang Peng Lyu Jin-Tong Guan Jie Cai Qing-Feng Guan Shun Guo School of materials science and engineering Jiangsu University School of material science and engineering Yancheng Institute of Technology engineering Institute of Advanced Manufacturing and Modern Equipment Technology Jiangsu University

This study investigates the influence of high-current pulsed electron beam（HCPEB） modification on the microstructure and shear strength of Cu/CuW joints.Reliable solid-state diffusion bonding of modified-Cu（MCu） and modified-CuW（M-CuW） was achieved by HCPEB modification pretreatment at a temperature of 800-900 ℃ and a pressure of 5 MPa for 10-50 min.Experiments demonstrate that HCPEB modification facilitates the dissolution of W and Cu,resulting in the formation of a Cu0.4W0.6solid solution and thus enhancing the uniform distribution of microstructures.Additionally,HCPEB-induced defects play a beneficial role in promoting the diffusion process by providing fast diffusion paths for elements.The optimal joints with the maximum shear strength of 213.7 MPa were obtained through bonding M-Cu and M-CuW at 900℃ and 5 MPa for 30 min,which attributes to the combined effects of fine-grained strengthening and solid solution strengthening.Overall,the application of HCPEB modification showcases its effectiveness in promoting element diffusion and enhancing the mechanical performance of the joints.

关键词： HCPEB Element diffusion Shear strength Crystal defects Surface modification

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Tuning the solubility of polysulfides for constructing practical lithium-sulfur battery

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Journal of Energy Chemistry 2024年第8期95卷 611-617页

作者： Jiapeng Li Jianlong Cong Haijin Ji Ting Shi Lixia Yuan Yunhui Huang State Key Laboratory of material Processing and Die & Mold Technology School of Materials Science and Engineering Huazhong University of Science and Technology

Li-S batteries are regarded as one of the most promising candidates for next-generation battery systems with high energy density and low cost.However,the dissolution-precipitation reaction mechanism of the sulfur（S） cathode enhances the kinetics of the redox processes of the insulating sulfu r,which also arouses the notorious shuttle effect,leading to serious loss of S species and corrosion of Li anode.To get a balance between the shuttle restraining and the kinetic property,a combined strategy of electrolyte regulation and cathode modification is proposed via introducing 1,1,2,2-tetrafluoroethyl-2,2,3,3-tetrafluoroprpyl ether（HFE） instead of 1,2-dimethoxyethane（DME）,and SeS7instead of S8.The introduction of HFE tunes the solvation structure of the LiTFSI and the dissolution of intermediate polysulfides with Se doping（LiPSSes）,and optimize the interface stability of the Li anode simultaneously.The minor Se substitution compensates the decrease in kinetic due to the decreased solubility of LiPSs.In this way,the Li-SeS7batteries deliver a reversible capacity of 1062 and 1037 mAh g-1with 2.0 and 5.5 mg SeS7cm-2loading condition,respectively.Besides,an electrolyte-electrode loading model is established to explain the relationship between the optimal electrolyte and cathode loading.It makes more sense to guide the electrolyte design for practical Li-S batteries.

关键词： Interface Li-S batteries Lithium polysulfides Se doping Shuttle effect Solubility

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