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Recently deepened insights regarding Mg corrosion and advanced engineering applications of Mg alloys

Journal of Magnesium and Alloys 2023年第11期11卷 3948-3991页

作者： Guang-Ling Song Andrej Atrens Department of Ocean Science and Engineering Southern University of Science and Technology1088 Xueyuan BoulevardShenzhen 518055China The University of Queensland School of Mechanical and Mining EngineeringCentre for Advanced Materials Processing and Manufacturing(AMPAM)St LuciaQld 4072 Australia State Key Laboratory of Physical Chemistry of Solid Surfaces Xiamen University422 S.Siming RdXiamen 361005China

This review summarizes recent insights into the Mg corrosion mechanism, clarifies many critical controversial points regarding the Mg corrosion behaviour, and updates some efforts made to extend the industrial application of Mg alloys. Based on the new understandings gained so far, future research directions are also suggested in the review. This review has the following logic. The first section "1. Scope"is a consolidation of the new understandings or developments regarding the Mg corrosion mechanism and the new applications for Mg alloys. It also highlights some key points for the review. The second section "2. Widely accepted knowledge" briefly summarizes the general understanding of Mg corrosion gained so far, which acts as the foundation for the following sections. The third section "3. Recently deepened insights" mainly briefs on some new insights into Mg corrosion phenomena based on recent findings. Different interpretations on the corrosion behaviours are comprehensively discussed in the fourth section "4. Controversial points" and the conclusions are drawn in the subsection"4.5 Clarified points". Apart from the fundamental understandings, various efforts in the application of Mg alloys are presented in the fifth section "5. New applications". Following the research tendency as indicated in the review, prioritized research areas are suggested in "*** directions". The review is concluded with "7. Concluding remarks" at last.

关键词： Mg Corrosion Hydrogen Anode Intelligentization

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Oxidation behavior of non-stoichiometric(Zr,Hf,Ti)C_(x) carbide solid solution powders in air

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Journal of advanced Ceramics 2021年第4期10卷 741-757页

作者： Huilin LUN Yi ZENG Xiang XIONG Ziming YE Zhongwei ZHANG Xingchao LI Haikun CHEN Yufeng LIU State Key Laboratory of Powder Metallurgy Central South UniversityChangsha 410083China Institute of Advanced Structure Technology Beijing Institute of TechnologyBeijing 100081China Science and Technology of Advanced Functional Composites Laboratory Aerospace Research Institute of Materials&Processing TechnologyBeijing 100076China

Multi-component solid solutions with non-stoichiometric compositions are characteristics of ultra-high temperature carbides as promising materials for hypersonic ***,for group IV transition-metal carbides,the oxidation behavior of multi-component non-stoichiometric(Zr,Hf,Ti)C_(x)carbide solid solution has not been clarified *** present work fabricated four kinds of(Zr,Hf,Ti)C_(x)carbide solid solution powders by free-pressureless spark plasma sintering to investigate the oxidation behavior of(Zr,Hf,Ti)C_(x)in *** effects of metallic atom composition on oxidation resistance were *** results indicate that the oxidation kinetics of(Zr,Hf,Ti)C_(x)are composition dependent.A high Hf content in(Zr,Hf,Ti)C_(x)was beneficial to form an amorphous Zr-Hf-Ti-C-0 oxycarbide layer as an oxygen barrier to enhance the initial oxidation ***,an equiatomic ratio of metallic atoms reduced the growth rate of(Zr,Hf,Ti)O_(2)oxide,increasing its phase stability at high temperatures,which improved the oxidation activation energy of(Zr,Hf,Ti)C_(x).

关键词： ultra-high temperature ceramics(UHTCs) (Zr,Hf,Ti)C_(x)carbides oxidation behavior oxidation resistance free-pressureless spark plasma sintering

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Bioinspired mechanically interlocking holey graphene@SiO_(2)anode

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Interdisciplinary materials 2022年第4期1卷 517-525页

作者： Fei Wang Xiaobin Liao Haoyu Wang Yan Zhao Jian Mao Donald G.Truhlar College of Materials Science and Engineering Sichuan UniversityChengduChina State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhanChina School of Materials Science and Engineering University of New South WalesSydneyNew South WalesAustralia The Institute of Technological Sciences Wuhan UniversityWuhanChina Department of Chemistry Chemical Theory CenterMinnesota Supercomputing InstituteUniversity of MinnesotaMinneapolisMinnesotaUSA

Mechanically interlocking structures that can enhance adhesion at the interface and regulate the stress distribution have been widely observed in biological *** by the biological structures in the wings of beetles,we synthesized a holey graphene@SiO_(2)anode with strong mechanical interlocking,characterized it electrochemically,and explained its performance by finite element analysis and density functional calcula*** mechanically interlocking structure enhances lithium-ion(Li^(+))storage by transmitting the strain from SiO_(2)to the holey graphene and by a mechano-electrochemical coupling *** interlocking fit hinders the abscission of SiO_(2)and the distinctive structure reduces the stress and strain of SiO_(2)during(de)*** positive mechano-electrochemical coupling effect preserves the amount of electrochemically active phase(LixSi)during cycles and facilitates Li+***,the capacity shows only a slight attenuation after 8000 cycles(cycling stability),and the specific capacity is~1200 mA h g^(−1)at 5 A/g(rate-performance).This study furnishes a novel way to design high-performance Li^(+)/Na+/K^(+)/Al3^(+)anodes with large volume expansion.

关键词： holey graphene mechanically interlocking mechano-electrochemical coupling effect simulation SiO_(2) anode

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Pulse-potential electrochemistry to boost real-life application of pseudocapacitive dual-doped polypyrrole

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SmartMat 2022年第4期3卷 644-656页

作者： Fang-Fang Sun Wen-Han Li Zi-Hang Huang Wenping Sun Yuhai Dou Ding Yuan Baohua Jia Tianyi Ma Key Laboratory for Green Synthesis and Preparative Chemistry of Advanced Materials Institute of Clean Energy ChemistryCollege of ChemistryLiaoning UniversityShenyangChina School of Science RMIT UniversityMelbourneVictoriaAustralia School of Materials Science and Engineering State Key Laboratory of Clean Energy UtilizationZhejiang UniversityHangzhouChina Shandong Institute of Advanced Technology JinanChina Institute for Superconducting&Electronic Materials University of WollongongWollongongAustralia

Polypyrrole(PPy)is a very promising pseudocapacitive electrode material for ***,the poor electrochemical performances and cycling stability caused by volumetric change and counterion drain severely limited its practical application and ***,we present a pulsepotential polymerization strategy for uniformly depositing a dual-doped PPy with ordered and shorter molecular structure by balancing the concentration *** a strategy ensures more homogeneous stress distribution of PPy during ultralong cycling tests and improves the cycle ***,the pulse-potential polymerized PPy with dual anion doping behavior induces enhanced protonation level and improved electrical conductivity,which boosting the charge transfer ***,the as-synthesized PPy exhibits a remarkable capacitance performance(7250 mF/cm^(2)@3 mA/cm^(2)),outstanding rate capability(3073 mF/cm^(2)@200 mA/cm^(2))and a long cycle *** assembled symmetric and asymmetric supercapacitors(ASC)exhibit good energy densities(0.8 mWh/cm^(2) for ASC and 0.5 mWh/cm^(2) for symmetric supercapacitor),and excellent durability with zero capacitive loss after 35,000 *** addition,we have fabricated small pouch devices,which can effectively operate a variety of electronic products(including the high-voltage 5 V smartphone,and tablet)and well withstand the external extreme tests during operation,demonstrating the quantitative investigation of the real-life application of aqueous supercapacitors.

关键词： dual-doping energy storage polypyrrole pouch-type device pseudocapacitive pulse-potential polymerization

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Simpler and Greener Preparation of An In-Situ Polymerized Polyimide Anode for Lithium Ion Batteries

SSRN

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SSRN 2023年

作者： Zhang, Qiuyitong Xu, Yuexin Lv, Ning Li, Hanyang Wei, Zijie Tiana, Tian Wang, Yadong Tang, Haolin State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China Foshan Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong Laboratory Xianhu Hydrogen Valley Foshan528200 China

A simplified and greener procedure for in-situ obtaining polyimide anode materials for lithium-ion battery electrodes is developed. The combined polyimide material synthesis and electrode preparation reduces the number of processing steps and treatment duration and decreases the energy required for heat treatment, solvent evaporation, and organic solvent use. More importantly, polymerization in situ on the electrode surface render the polyimide particles a sea urchin-like structure, leading to fast electrochemical kinetics, and significant improvement in discharge capacity and cycling performance compared with materials obtained using traditional procedures. Specific capacities of 1870 mAh g-1 and 2277 mAh g-1 at 30℃ and 60℃, respectively, are obtained. A capacity of 1774 mAh g-1 is retained after 500 cycles at high current density of 1000 mA g-1 at 60℃. This new preparation process not only simplifies the preparation process and makes it greener, but also significantly improves the battery performance, providing new possibilities for the preparation of high-performance low-cost lithium-ion battery electrodes. © 2023, The Authors. All rights reserved.

关键词： Solvents

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Erosion-corrosion resistance of Mo-Ti- and Ni-Cr-Mo-alloyed medium-carbon martensitic steels: a critical analysis of synergistic effect of erosion and corrosion

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Journal of Iron and Steel Research International 2022年第8期29卷 1299-1311页

作者： De-fa Li Hang-yu Dong Cheng-yang Hu Kai-ming Wu Serhii Yershov Oleg Isayev School of Mechanical and Vehicle Engineering West Anhui UniversityLuan 237012AnhuiChina The State Key Laboratory of Refractories and Metallurgy Hubei Province Key Laboratory of Systems Science on Metallurgical ProcessingInternational Research Institute for Steel TechnologyWuhan University of Science and TechnologyWuhan 430081HubeiChina Laboratory for Excellence in Advanced Steel Research Materials Science and Engineering ProgramDepartment of MetallurgicalMaterials and Biomedical EngineeringUniversity of Texas at El PasoEl PasoTX 79968USA

Grain refinement renders Mo-Ti-alloyed medium-carbon martensitic steel to exhibit high hardness,high strength,and good toughness,but the erosion-corrosion resistance of steel in a corrosive slurry environment is not ***-Ti-alloyed medium-carbon martensitic steel is compared with Ni-Cr-Mo-alloyed medium-carbon martensitic steel,and the erosion-corrosion resistance of those two steels under impingement by NaCl solution with gravels has been *** components,pure-corrosion rate,pure-erosion rate,and synergistic effect of erosion and corrosion(SEEC)of erosion-corrosion rate,were *** pure-corrosion and pure-erosion rates of Mo-Ti-alloyed steel were higher than those of Ni-Cr-Mo-alloyed one;however,its erosion-corrosion rate was relatively lower because of a weak *** plastic deformation and work hardening due to gravel impingement were the essential reason for SEEC,which could be reduced by grain refinement,and consequently,Mo-Ti-alloyed steel with finer grains had better erosion-corrosion *** refinement could be an effective way to improve the erosion-corrosion resistance of martensitic steels.

关键词： Grain refinement Mo-Ti alloying Ni-Cr-Mo alloying Martensite Erosion-corrosion

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Surface-assembled highly flexible Na_(3)(VOPO_(4))_(2)F nanocube cathode for high-rate binder-free Na-ion batteries

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Chinese Chemical Letters 2021年第2期32卷 826-829页

作者： Bohua Deng Ning Yue Haoyang Dong Qiuyue Gui Liang Xiao Jinping Liu School of Chemistry Chemical Engineering and Life ScienceWuhan University of TechnologyWuhan 430070China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology.Wuhan 430070China Key Laboratory for Photonic and Electronic Bandgap Materials Ministry of EducationSchool of Physics and Electronic EngineeringHarbin Normal UniversityHarbin 150025China

Flexible Na-ion storage cathodes are still very few due to the challenge in achieving both reliable mechanical flexibility and excellent electrochemical ***,a new type of flexible Na_(3)(VOPO_(4))_(2)F cathode with nanocubes tightly assembled on carbon cloth is fabricated by a facile solvothe rmal method for the first *** cathode is able to exhibit superior rate capability and stable cycling performa nce up to 1000 cycles,due to the surface-assembling of crystalline nanocubes on carbon *** addition,it shows good mechanical flexibility,nearly no capacity decay is observed after continuous bending of 500 *** this novel cathode and a directly-grown Na_(2)Ti_(2)O_(5) anode,a fully binde r-free Na-ion battery is *** can deliver a high wo rking voltage and increased gravimetric energy/power densities(maximum values:220.2 Wh/kg;5674,7 W/kg),and can power a LED indicator at bending angles fro m 0° to 180°.

关键词： Flexible cathode Na_(3)(VOPO_(4))_(2)F Nanocube Surface-assembling Sodium-ion battery

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Elevating the d-Band Center of Ni3S2Nanosheets by Fe Incorporation to Boost the Oxygen Evolution Reaction

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Langmuir 2023年第15期39卷 5375-5383页

作者： Jie Ying Zhen-Zhao He Jiang-Bo Chen Yu-Xuan Xiao Xiao-Yu Yang School of Chemical Engineering and Technology Sun Yat-sen University Zhuhai 519082 China State Key Laboratory Advanced Technology for Materials Synthesis and Processing & School of Materials Science and Engineering & Shenzhen Research Institute & Joint Laboratory for Marine Advanced Materials in Pilot National Laboratory for Marine Science and Technology (Qingdao) Wuhan University of Technology 122 Luoshi Road Wuhan 430070 China

Many attempts have been made to enhance the relatively poor electrochemical activity of Ni3S2 for the oxygen evolution reaction (OER) by elevating the d-band center. Unfortunately, only limited suc...

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Boosting oxygen evolution of LiCoO2 electrocatalysts via lithium defect

Materials Today Catalysis

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materials Today Catalysis 2025年 8卷

作者： Li, Huamei Li, Mengyuan Liao, Lingling Yang, Han Xiang, Kun Luo, Guoqiang Xie, Mingjiang School of Chemistry and Environmental Engineering Engineering Research Center of Phosphorus Resources Development and Utilization of Ministry of Education Wuhan Institute of Technology Wuhan430205 China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China Hubei Key Lab for Processing and Application of Catalytic Materials College of Chemical Engineering Huanggang Normal University Huanggang438000 China

The challenge of the complex oxygen evolution reaction (OER) currently impedes the efficient production of hydrogen via electrolytic water splitting. To address this issue, the development and improvement of effective electrocatalysts are required. LiCoO2, a key material in lithium-ion batteries, has shown promising potential as an electrocatalyst for electrochemical energy conversion. However, OER catalysts derived from LiCoO2 have faced obstacles such as high overpotential and a complicated preparation process. In this study, the preparation method is adjusted to optimize the synthesis of Li1-xCoO2 with a defective structure, resulting in an impressive overpotential of only 290 mV at a current density of 100 mA cm−2 and a remarkable Tafel slope of 15.2 mV dec−1. The exceptional catalytic activity of Li1-xCoO2 can be attributed to the absence of Li, which triggers oxidative alterations in the electronic structure of Co. Density functional theory (DFT) calculations reveal that Li defects can influence the d-band center of active Co sites, enhancing the adsorption capabilities of Co sites towards *OOH intermediates and increasing the conductivity of the electrocatalyst during the OER process. These alterations improve the velocity of the crucial step in the reaction, ultimately boosting the catalyst's overall performance and efficiency. © 2024 The Authors

关键词： Lithium-ion batteries

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Polyphenol Synergistic Cerium Oxide Surface Engineering Constructed Core-Shell Nanostructures as Antioxidants for Durable and High-Performance Proton Exchange Membrane Fuel Cells

SSRN

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SSRN 2023年

作者： Tang, Haolin Zhao, Shengqiu Liao, Yucong Wang, Rui Liu, Guoliang Zhang, Haining State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China Foshan Xianhu Laboratory The Advanced Energy Science and Technology Guangdong Laboratory Xianhu Hydrogen Valley Foshan528200 China

The chemical degradation of proton exchange membranes (PEMs) suffering from radical attack is a crucial issue in the development of proton exchange membrane fuel cells (PEMFCs), while incorporating cerium oxide (CeO2) nanoparticles (NPs) with regenerative redox properties to eliminate radicals could effectively alleviate degradation. However, the low stability and restricted activity of CeO2 in the PEMFC operating condition and the poor compatibility with PEM due to CeO2 agglomeration stimulate the urgency for structural modulation of CeO2. Herein, polyphenols surface functionalized CeO2 core-shell structure (CeO2@TP) were constructed via assembling oxidation-induced coupling tea polyphenols (TP) on CeO2 NPs. The TP oligomeric shell as a protective layer enhances the stability of CeO2, mitigating radical scavenging activity degradation and improving compatibility with PEMs. Gratifyingly, the phenolic hydroxyl-rich reductive TP oligomeric shell accelerates the regeneration of Ce(IV) to Ce(III), increasing the proportion of Ce(III) and oxygen vacancies on the CeO2 surface, thus boosting antioxidation efficiency. As a result, the CeO2@TP-based PEMs exhibited an OCV decay rate of 0.22 mV h-1, a maximum power density of 1.06 W cm-2, an H2 crossover value of 2.18 mA cm-2, thickness retention (91.1%), and negligible Ce migration after 404 hours of accelerated degradation testing. © 2023, The Authors. All rights reserved.

关键词： Oligomers

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