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Alternative Strategy for Development of Dielectric Calcium Copper Titanate‑Based Electrolytes for Low‑Temperature Solid Oxide Fuel Cells

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Nano-Micro Letters 2025年第1期17卷 310-332页

作者： Sajid Rauf Muhammad Bilal Hanif Zuhra Tayyab Matej Veis MAKYousaf Shah Naveed Mushtaq Dmitry Medvedev Yibin Tian Chen Xia Martin Motola Bin Zhu College of Mechatronics and Control Engineering Shenzhen UniversityShenzhen 518060People’s Republic of China Department of Inorganic Chemistry Faculty of Natural SciencesComenius University BratislavaIlkovicova684215 BratislavaSlovakia Energy Storage Joint Research Center School of Energy and EnvironmentSoutheast UniversityNanjing 210096People’s Republic of China hydrogen Energy Laboratory Ural Federal University620002 EkaterinburgRussia Laboratory of Electrochemical Devices Based on Solid Oxide Proton Electrolytes Institute of High Temperature Electrochemistry620066 EkaterinburgRussia School of Microelectronics Hubei UniversityWuhan 430062People’s Republic of China

The development of low-temperature solid oxide fuel cells(LT-SOFCs)is of significant importance for realizing the widespread application of *** has stimulated a substantial materials research effort in developing high oxide-ion conductivity in the electrolyte layer of *** this context,for the first time,a dielectric material,CaCu_(3)Ti_(4)O_(12)(CCTO)is designed for LT-SOFCs electrolyte application in this *** individual CCTO and its heterostructure materials with a p-type Ni_(0.8)Co_(0.15)Al_(0.05)LiO_(2−δ)(NCAL)semiconductor are evaluated as alternative electrolytes in LT-SOFC at 450–550℃.The single cell with the individual CCTO electrolyte exhibits a power output of approximately 263 mW cm^(-2) and an open-circuit voltage(OCV)of 0.95 V at 550℃,while the cell with the CCTO–NCAL heterostructure electrolyte capably delivers an improved power output of approximately 605 mW cm^(-2) along with a higher OCV over 1.0 V,which indicates the introduction of high hole-conducting NCAL into the CCTO could enhance the cell performance rather than inducing any potential short-circuiting *** is found that these promising outcomes are due to the interplay of the dielectric material,its structure,and overall properties that led to improve electrochemical mechanism in CCTO–***,density functional theory calculations provide the detailed information about the electronic and structural properties of the CCTO and NCAL and their heterostructure CCTO–*** study thus provides a new approach for developing new advanced electrolytes for LT-SOFCs.

关键词： LT-SOFCs Dielectric CaCu_(3)Ti_(4)O_(12) Semiconductor Ni_(0.8)Co_(0.15)Al_(0.05)LiO_(2−δ) Ionic conductivity Heterostructure electrolyte

hydrogen sorption properties of Mg-20wt.%Fe_(23)Y_(8) composite prepared by reactive mechanical alloying

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Rare Metals 2006年第z1期25卷 247-251页

作者： LI Zhinian LIU Xiaopeng HUANG Zuo JIANG Lijun WANG Shumao hydrogen Material&Technology Research institute General Research Institute for Nonferrous MetalBeijing100088China

Mg-20wt.%Fe_(23)Y_(8) composite was successfully prepared by reactive mechanical alloying(RMA).X-ray diffraction(XRD)measurement shows that the main phases of composite are MgH_(2) and *** composite exhibits excellent hydrogen abs/desorption properties and can absorb 4.36wt.%and 5.72wt.%hydrogen at 473 and 573 K in 10 min under 3.0 MPa hydrogen pressure,*** composite can desorb 5.27wt.%hydrogen at 573 K in 30 min under 0.02 MPa hydrogen *** with the pure MgH_(2),the hydrogen desorption temperature of Mg-20wt.%Fe_(23)Y_(8) composite is decreased about 40℃.It is supposed that both the catalyst effect of Fe-Y distributed in Mg substrate and the crystal defects play the main role in improving hydrogen sorption properties of Mg-20wt.%Fe_(23)Y_(8) composite.

关键词： hydrogen storage composite magnesium mechanical alloying P-C-T and Mg_(2)FeH_(6)

Lattice Boltzmann simulation study of anode degradation in solid oxide fuel cells during the initial aging process

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International Journal of Minerals,Metallurgy and Materials 2024年第2期31卷 405-411页

作者： Shixue Liu Zhijing Liu Shuxing Zhang Hao Wu hydrogen Energy Industrial Technology Innovation Center China Nuclear Power Technology Research InstituteShenzhen 518031China Shenzhen Engineering Research Center for hydrogen Safety Shenzhen 518031China

For present solid oxide fuel cells(SOFCs),rapid performance degradation is observed in the initial aging process,and the dis-cussion of the degradation mechanism necessitates quantitative ***,focused ion beam-scanning electron microscopy was em-ployed to characterize and reconstruct the ceramic microstructures of SOFC *** lattice Boltzmann method(LBM)simulation of multiphysical and electrochemical processes in the reconstructed models was *** samples collected from industrial-size cells were characterized,including a reduced reference cell and a cell with an initial aging *** parameters of the reconstructed microstructures revealed a significant decrease in the active triple-phase boundary and Ni connectivity in the aged cell compared with the reference *** LBM simulation revealed that activity degradation is dominant compared with microstructural degradation during the initial aging process,and the electrochemical reactions spread to the support layer in the aged *** microstructural and activity de-gradations are attributed to Ni migration and coarsening.

关键词： solid oxide fuel cell anode degradation focused ion beam-scanning electron microscopy lattice Boltzmann method

Electrospinning of Nylon-6,6 Solutions into Nanofibers: Rheology and Morphology Relationships

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Chinese Journal of Polymer Science 2014年第6期32卷 793-804页

作者： Ali Abbasi Mohamed Mahmoud Nasef Matsuura Takeshi Reza Faridi-Majidi Faculty of Chemical Engineering Universiti Teknologi Malaysia institute of hydrogen economy International Campus Universiti Teknologi Malaysia Malaysia-Japan International institute of Technology International Campus Universiti Teknologi Malaysia Department of Chemical & Biological Engineering University Ottawa Department of Medical Nanotechnology School of Advanced Medical Technologies Tehran University of Medical Sciences

The relationship between the rheological properties of nylon-6,6 solutions and the morphology of their electrospun nanofibers was established. The viscosity of nylon-6,6 in formic acid （90%） was measured in the concentration range of 5 wt%-25 wt% using a programmable viscometer. Electrospinning of nylon-6,6 solutions was carried out under controlled parameters. The chemical structure, morphology and thermal properties of the obtained nanofibers were investigated using Fourier transform infrared spectroscopy （FTIR）, scanning electron microscopy （SEM） and differential scanning calorimetry （DSC）, respectively, Entanglement concentration （ce） was found to be 15 wt% and a power law relationship between specific viscosity and solution concentration was observed with exponents of 2.0 and 3.3 for semi-dilute unentangled （c 〈 ce） and semi-dilute entangled （c 〉 ce） regimes, respectively. The diameter and uniformity of the nanofibers were found to be dependent on the viscosity. Moreover, the average diameter of electrospun nanofibers was found to be dependent on zero shear rate viscosity and normalized concentration （c/ce） in a power law relationship with exponents of 0.298 and 0.816, respectively. For nylon-6,6 solutions, the entanglement concentration （ce = 15 wt%） provides the threshold viscosity required for the formation of a stable polymeric jet during electrospinning and producing uniform beadless fibers. For concentrations less than ce, beaded fibers with some irregularities are formed. DSC analysis showed an increase in crystallinity of all electrospun samples compared to original polymer. Furthermore; Based on FTIR spectroscopy, α phase is dominant in electrospun nanofibers and minor amount offland ）,phases is also available.

关键词： Nylon-6,6 electrospinning Viscosity Nanofibers Entanglement concentration Crystallinity.

Deciphering the role of mtH2O2 in hepatic ischemia-reperfusion injury mechanisms with low-background super-resolution fluorogenic probe

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Science China Chemistry 2025年第01期 297-307页

作者： Bin Fang Limin Wang Haoqin Li Jiaxin Zhang Yang Ding Pan Pan Li Bo Peng Hua Bai Lin Li Frontiers Science Center for Flexible Electronics Xi'an Institute of Flexible Electronics (IFE) and Xi'an Institute of Biomedical Materials &Engineering Northwestern Polytechnical University institute of Flexible Electronics (IFE Future Technologies) Xiamen University

Hepatic ischemia-reperfusion injury（HIRI） is characterized by mitochondrial dysfunction and oxidative stress. Monitoring mitochondrial hydrogen peroxide（mtH2O2） levels in real-time through super-resolution imaging is crucial for elucidating its distribution in live cells and its mechanism of action during HIRI. However, low-background fluorogenic probes have been overlooked in the context of super-resolution imaging. In this study, we developed a low-background fluorogenic probe（MitoWG） with the potential for super-resolution morphology-correlated mitochondrial identification to track the fluctuates of mtH2O2in HIRI. Activation of the desirable fluorescence properties of the probe by mtH2O2was confirmed using structural illumination microscopy（SIM）, enabling high-quality mitochondrial imaging with exceptional specificity and *** in mtH2O2levels were successfully observed in both cellular and rat models of HIRI. Furthermore, we associated the decline in mitochondrial redox homeostasis with accelerated mtH2O2production during HIRI, which triggered mitophagy deficiency and led to cell death. In conclusion, Mito-WG possesses excellent photophysical and low-background properties for SIM imaging, making it a promising tool for mtH2O2tracking in HIRI research and clinical diagnosis.

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A novel bimetallic RuFe nanocluster to enable highly efficient oxygen reduction in zinc-air batteries

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Progress in Natural Science:Materials International 2022年第6期32卷 769-775页

作者： Yang Li Duowen Ma Yuetao Wang Haibin Yang Zirui Lou Runzhi Qin Qinghe Zhao Feng Pan Huakun Liu School of Advanced Materials Peking University Shenzhen Graduate School hydrogen Energy institute Zhejiang University institute for Superconducting and Electronic Materials University of Wollongong

Zinc-air batteries(ZABs) have the advantages of high energy density and safety but their large-scale application is hindered by sluggish kinetics of four-electron aqueous O2redox *** used Ruthenium(Ru)-based catalysts possess intrinsic oxygen evolution catalytic activity but suffer from insufficient oxygen reduction reaction(ORR) ***,to optimize the ORR activity of Ru-based catalyst,an iron(Fe)-coordinated,bimetallic RuFe cluster is constructed and homogeneously dispersed within nitrogen(N)-doped carbon layers(denoted as RuFe@NC).Benefitting from the optimized ORR activity and more active site exposure,the RuFe@NC exhibits superior ORR activity with a half wave potential(E1/2) of 0.88 V higher than that of Pt/C(0.82 V).Accordingly,the RuFe@NC-based ZAB outperforms the Pt/C+IrO2-based device,presenting a reduced polarization of 0.7 V and an enhanced cycling lifetime of 50 h at 10 mA ***,the optimized structural design ultralow Ru loading(0.013 mgRucm-2) overcomes the cost barriers and demonstrates its high *** bimetallic RuFe nanocluster opens a new way for future design of more efficient and stable catalytic systems.

关键词： Oxygen reduction reaction Bimetallic nanocluster Ru-based electrocatalyst Zinc-air battery

RADIATION GRAFTED POLY(VINYLIDENE FLUORIDE)-GRAFT-POLYSTYRENE SULFONIC ACID MEMBRANES FOR FUEL CELLS:STRUCTURE-PROPERTY RELATIONSHIPS

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Chinese Journal of Polymer Science 2010年第5期28卷 761-770页

作者： Mohamed Nasef Hamdani Saidi Khairulzaman Mohd Dahlan institute of hydrogen economy Universiti Teknologi MalaysiaInternational City CampusJalan Semarak54100 Kuala LumpurMalaysia Faculty of Chemical and Natural Resources Engineering Universiti Teknologi Malaysia81310 UTM SkudaiJohorMalaysia Radiation Processing Technology Division Malaysian Nuclear AgencyBangi43000 KajangSelangorMalaysia

Structure-property relationships for poly（vinylidene fluoride）-graft-polystyrene sulfonic acid （PVDF-g-PSSA） fuel cell membranes prepared by a single step method involving radiation-induced grafting of sodium styrene sulfonate （SSS） onto electron beam （EB） irradiated poly（vinylidene fluoride）（PVDF） films were established. The physico-chemical properties of the membranes such as ion exchange capacity, water swelling and proton conductivity were correlated with the degree of grafting （G, %） and the structural changes taking place in the membrane matrix during the preparation procedure. The variation in the crystallinity and the thermal stability of membranes was studied by differential scanning calorimetry （DSC） and thermogravimetric analysis （TGA）, respectively. The membranes were found to undergo substantial structural changes in forms of ionic sites increase, hydrophilicity enhancement, hydrophobicity reduction and crystallinity decrease with the variation in G （%） and the preparation method. The structural and thermal properties of the obtained membranes were also compared with their counterparts prepared by a conventional two-steps method i.e. radiation induced grafting of styrene onto EB irradiated PVDF films followed by sulfonation. The PVDF-g-PSSA membranes obtained by a single-step method were found to have superior properties compared to those obtained by the conventional two-steps method.

关键词： PVDF films Sodium styrene sulfonate Radiation-induced grafting Proton exchange membranes.

Dielectric-ion-conductive ZnNb2O6 layer enabling rapid desolvation and diffusion for dendrite-free Zn metal batteries

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Journal of Energy Chemistry 2025年第1期100卷 693-701页

作者： Haifeng Yang Jian Wang Panpan Zhang Xiaomin Cheng Qinghua Guan Jing Dong Bixian Chen Lujie Jia Jing Zhang Yongzheng Zhang Yunjian Liu Hongzhen Lin School of Materials Science and Engineering Jiangsu University i-Lab & CAS Key Laboratory of Nanophotonic Materials and Devices Suzhou Institute of Nano-Tech and Nano-Bionics Chinese Academy of Sciences Helmholtz institute Ulm (HIU) Karlsruhe institute of Technology (KIT) School of Materials Science and Engineering Xi'an University of Technology State Key Laboratory of Chemical Engineering East China University of Science and Technology

Rechargeable aqueous zinc-metal batteries （AZMBs） are promising candidates for large-scale energy storage systems due to their low cost and high ***,their performance and sustainability are significantly hindered by the sluggish desolvation kinetics at the electrode/electrolyte interface and the corresponding hydrogen evolution reaction where active water molecules tightly participate in the Zn（H2O）62+solvation ***,learnt from self-generated solid electrolyte interphase （SEI） in anodes,the dielectric but ion-conductive zinc niobate nanoparticles artificial layer is constructed on metallic Zn surface （ZNB@Zn）,acting as a rapid desolvation *** zincophilic and dielectric-conductive properties of ZNB layer accelerate interfacial desolvation/diffusion and suppress surface corrosion or dendrite formation,achieving uniform Zn plating/stripping behavior,as confirmed by electronic/optical microscopies and interface spectroscopical measurements together with theoretical ***,the as-prepared ZNB@Zn electrode exhibits excellent cycling stability of over 2000 h and robust reversibility （99.54%） even under high current density and depth of discharge ***,the assembled ZNB@Zn-based full cell displays high capacity-retention rate of 80.21%after 3000 cycles at 5 A g-1and outstanding rate performance up to 10 A *** large-areal pouch cell is stabilized for hundreds of cycles,highlighting the bright prospects of the dielectric but ion-conductive layer in further application of AZMBs.

关键词： Zn metal battery Dielectric artificial layer Rapid ion diffusion Zincophilic diffusion Active water inhibition

Boosting hydrocarbon conversion via Cu-doping induced oxygen vacancies on CeO2 in CO2 electroreduction

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Journal of Energy Chemistry 2025年第1期100卷 66-76页

作者： Lei Xue Tong Shi Chenhui Han Heng Zhang Fenrong Liu Haorun Li Yan Wang Xiaojun Gu Shanghong Zeng Inner Mongolia Key Laboratory of Chemistry and Physics of Rare Earth Materials School of Chemistry and Chemical Engineering Inner Mongolia University State Key Laboratory of Coal Conversion Institute of Coal Chemistry Chinese Academy of Sciences institute of Catalysis Department of Chemistry Zhejiang University National Key Laboratory of Baiyunobo Rare Earth Resource Research and Comprehensive Utilization Baotou Research Institute of Rare Earths

Conversion of CO2back to hydrocarbons is the most direct way of closing the“carbon cycle”,and its significance is further enlarged if this process is driven by renewable energies such as ***,precisely controlling the product selectivity towards hydrocarbons against the competitive hydrogen evolution remains challenging,especially for Cu-based ***,we report a novel defect engineering strategy,by which Cu-doping-induced oxygen vacancies on CeO2nanorods were effectively created,with adjustable vacancy/Cu *** resulting optimum catalyst shows up to 79% catalytic current density to hydrocarbons （excluding CO）,with 49% faradaic efficiency to *** and density functional theory unveil that the ratio between oxygen vacancy and Cu affects significantly the formation of*CHO and activation of H2O,which leads to the following deep hydrogenation to *** findings may spur new insights for designing and developing more controllable chemical process relevant to CO2utilization.

关键词： Oxygen vacancy Hydrocarbon production Reaction mechanism