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Electromagnetic wave absorption and mechanical properties of SiC nanowire/low-melting-point glass composites sintered at 580°C in air

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International Journal of Minerals,Metallurgy and materials 2023年第9期30卷 1809-1815页

作者： Ranran Shi Wei Lin Zheng Liu Junna Xu Jianlei Kuang Wenxiu Liu Qi Wang Wenbin Cao Department of Inorganic Nonmetallic Materials School of Materials Science and EngineeringUniversity of Science and Technology BeijingBeijing 100083China National Demonstration Center for Materials Education Institute for Advanced Materials and TechnologyUniversity of Science and Technology BeijingBeijing 100083China Beijing Institute of Aeronautical Materials Aero Engine Corporation of ChinaBeijing 100095China School of Materials and Environmental Engineering Hunan University of HumanitiesScience and TechnologyLoudi 417000China

Si C nanowires are excellent high-temperature electromagnetic wave (EMW) absorbing materials. However, their polymer matrix composites are difficult to work at temperatures above 300℃, while their ceramic matrix composites must be prepared above 1000℃ in an inert atmosphere. Thus, for addressing the abovementioned problems, SiC/low-melting-point glass composites were well designed and prepared at 580℃ in an air atmosphere. Based on the X-ray diffraction results, SiC nanowires were not oxidized during air atmosphere sintering because of the low sintering temperature. Additionally, SiC nanowires were uniformly distributed in the glass matrix material. The composites exhibited good mechanical and EMW absorption properties. As the filling ratio of SiC nanowires increased from 5wt%to 20wt%, the Vickers hardness and flexural strength of the composite reached HV 564 and 213 MPa, which were improved by 27.7%and 72.8%, respectively, compared with the low-melting-point glass. Meanwhile, the dielectric loss and EMW absorption ability of SiC nanowires at 8.2–12.4 GHz were also gradually improved. The dielectric loss ability of low-melting-point glass was close to 0. However, when the filling ratio of SiC nanowires was 20wt%, the composite showed a minimum reflection loss (RL) of-20.2 dB and an effective absorption (RL≤-10 dB) bandwidth of2.3 GHz at an absorber layer thickness of 2.3 mm. The synergistic effect of polarization loss and conductivity loss in SiC nanowires was responsible for this improvement.

关键词： SiC nanowires glass composite flexural strength dielectric properties microwave absorption

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Hydrothermal synthesis of polyimide-linked covalent organic frameworks towards ultrafast and stable cathodic sodium storage

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science China Chemistry 2024年第4期67卷 1300-1310页

作者： Xiya Yang Lei Gong Zhixin Liu Qianjun Zhi Baoqiu Yu Xin Chen Kang Wang Xiaofeng Li Dongdong Qi Jianzhuang Jiang Beijing Advanced Innovation Center for Materials Genome Engineering Beijing Key Laboratory for Science and Application of Functional Molecular and Crystalline MaterialsDepartment of Chemistry and Chemical EngineeringSchool of Chemistry and Biological EngineeringUniversity of Science and Technology BeijingBeijing 100083China State Key Laboratory of Organic-Inorganic Composites College of Materials Science and EngineeringBeijing University of Chemical TechnologyBeijing 100029China

Redox-active organic materials are capturing growing attention as cathode materials for sustainable alkaline metal ion ***,the storage of Na+in most organic materials-based cathodes is plagued by low capacity and unsatisfying rate performance due to their low active site densities and limited exposed active ***,two polyimide-linked covalent organic frameworks(COFs),namely HATN-PD-COF and HATN-TAB-COF,were fabricated from hydrothermal synthesis with redoxactive triphenylene-2,3,6,7,10,11-hexacarboxylic acid and aromatic amines as starting *** X-ray diffraction and electron microscopy analysis indicate the high crystalline nature of these COFs with AA stacking configuration and orderly mesoporous tunnel.N_(2) sorption measurement discloses the permanent porosity of these two COFs with a Brunauer-EmmettTeller surface area of 1,065-1,200 m^(2)g^(-1)and a large pore size of 2.0-3.1 *** intermittent titration technique and density functional theory calculations reveal the facile Na+ion diffusion along the mesoporous tunnel of these COFs with a small energy barrier of 0.13-0.40 e *** particular,the as-prepared COFs based-cathodes show ultrafast and stable Na+storage associated with their conjugated electronic structure,highly ordered mesoporous tunnel,robust structure,and redox-active C=N/C=O-rich framework as exemplified by the high reversible capacity of 210 m A h g^(-1)at 200 m A g^(-1),record-high rate performance(195 m A h g^(-1)at a high current density of 10,000 m A g^(-1))among organic electrodes and the capacity retention of nearly 91%at 10,000 m A g^(-1)after 7,000 cycles for HATN-PD-COF.

关键词： covalent organic framework sodium ion battery cathode high rate organic electrode

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Thermal Stability and Degeneration Behavior of Solar Selective Absorber Based on WTi-Al_(2)O_(3)Cermet

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Journal of Wuhan University of technology(materials science) 2024年第6期39卷 1555-1564页

作者： WANG Xiaobo FANG Wei MA Yuchao CHENG Xudong LI Kewei Department of Physics and Electronic Engineering Jinzhong UniversityJinzhong 030619China College of Materials Science and Engineering Taiyuan University of TechnologyTaiyuan 030024China State Key Laboratory of Advanced Technology for Materials Synthesis and Progressing Wuhan University of TechnologyWuhan 430070China

A WTi-Al_(2)O_(3)cermet-based solar selective absorber was prepared to investigate the atomic diffusion induced spectral selectivity *** as-deposited coating exhibits superior absorptance(0.934)and low thermal emittance(0.098),as well as excellent thermal stability with a selectivity of 0.900/0.07 even after annealing at 923 K for 400 h in Ar ***,the multilayer coating failed after being subjected to annealing at 923 K for 400 h in an air environment,as indicated by a decrease in solar absorptance to 0.912 and an increase in thermal emittance to *** microstructure characterizations reveal that the annealed coating exhibits a columnar morphology along the vertical direction of the *** presence of abundant grain boundaries in the multilayer coating promotes the outward diffusion of Cr and Mn atoms in the stainless-steel *** Mn atoms,in particular,possess the capability to migrate towards the surface of the coating and undergo an oxidation reaction with oxygen,facilitating the formation of a thick Mn_(2)O_(3)*** roughness of the coating surface was significantly increased in this case,adversely affecting solar absorptance due to amplified sunlight *** addition,the rocketing of thermal emittance is attributed to the destabilization of W infrared reflective layer during the *** findings highlight the importance of considering the outward diffusion of Mn and Cr elements in the stainless-steel substrate when optimizing solar selective absorbers.

关键词： solar selective absorber thermal stability spectral selectivity optical properties

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A new thiol-sulfur click chemistry for lithium-organosulfide batteries

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The Innovation 2025年第2期6卷 42-48,41页

作者： Rong Zou Wenwu Liu Fen Ran State Key Laboratory of Advanced Processing and Recycling of Non-ferrous Metals Department of Polymeric Materials EngineeringSchool of Materials Science and EngineeringLanzhou University of TechnologyLanzhou 730050China

Click chemistry is a rapid,reliable,and powerful function and a highly selective organic reaction that facilitates the efficient synthesis of various molecules by joining small *** approach has found widespread applications in fields such as drug development,chemical synthesis,and molecular *** recent years,the reaction of alkali-catalyzed polymerization of thiol and sulfur has been employed to prepare various sulfur-containing polymers,which are applied as electrochemical active electrode materials in the pursuit of good *** this study,it is surprising to find that the reaction mechanism exhibits characteristics of both the alkali-catalyzed sulfhydryl Micheal addition reaction and thiol-epoxy click chemistry;for the first time,thiol-sulfur click chemistry is defined in detail,providing a comprehensive description of its underlying scientific *** introduction of this new reaction pathway holds significant potential for advancing research and the development of sulfur-containing *** on this novel click chemistry,a new sulfur-containing polymer,polydivinylthioether hexasulfide,has been designed and successfully applied as a cathode material in lithium-organosulfide *** material demonstrates excellent electrochemical performance,achieving an initial capacity that reaches 790.5 mAh g−1(82.6%of theoretical capacity),and in a long-term cycle test,the capacity decay rate is only 0.063%after 1,000 cycles.

关键词： electrochemical active electrode mater thiol sulfur click chemistry molecular biologyin lithium organosulfide batteries synthesis various molecules organic reaction click chemistry joining small unitsthis

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Stable sodium anodes for sodium metal batteries(SMBs) enabled by in-situ formed quasi solid-state polymer electrolyte

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Journal of Energy Chemistry 2023年第2期77卷 290-299,I0008页

作者： Jian Ma Xuyong Feng Yueyue Wu Yueda Wang Pengcheng Liu Ke Shang Hao Jiang Xianglong Hou David Mitlin Hongfa Xiang School of Materials Science and Engineering Anhui Provincial Key Laboratory of Advanced Functional Materials and DevicesHefei University of TechnologyHefei 230009AnhuiChina Materials Science and Engineering Program&Texas Materials Institute(TMI) The University of Texas at AustinAustinTX 78712-1591USA School of Chemistry and Chemical Engineering Anhui Provincial Key Laboratory of Advanced Functional Materials and DevicesHefei University of TechnologyHefei 230009AnhuiChina

A high-performance quasi-solid polymer electrolyte for sodium metal batteries(SMBs)based on in-situ polymerized poly(1,3-dioxolane)(DOL)with 20%volume ratio of fluoroethylene carbonate(FEC),termed"PDFE-20",is proposed in this *** is demonstrated PDFE-20 possesses a room-temperature ionic conductivity of 3.31×10^(-3) S cm^(-1),an ionic diffusion activation energy of 0.10 eV,and an oxidation potential of 4.4 *** based on PDFE-20 and Na_(3)V_(2)(PO_(4))_(3)(NVP)cathodes were evaluated with an active material mass loading of 6.8 mg cm^(-2).The cell displayed an initial discharge specific capacity of 104 mA h g^(-1),and97.1%capacity retention after 100 cycles at 0.5 ***-situ polymerization conformally coats the anode/-cathode interfaces,avoiding geometrical gaps and high charge transfer resistance with ex-situ polymerization of the same *** acts as a plasticizer during polymerization to suppress crystallization and significantly improves ionic *** battery cycling FEC promotes mechanical congruence of electrolyte-electrode interfaces while forming a stable NaF-rich solid electrolyte interphase(SEI)at the *** functional theory(DFT)calculations were also performed to further understand the role FEC in the poly(DOL)-FEC *** work broadens the application of in-situ prepared poly(DOL)electrolytes to sodium storage and demonstrates the crucial role of FEC in improving the electrochemical performance.

关键词： Quasi-solid batteries(QSBs) Quasi-solid electrolytes(QSEs) NaF-rich passivating layer Interfacial stability Sodium metal batteries(SMBs)

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Binding SnO_(2)Nanoparticles with MoS_(2)Nanosheets Toward Highly Reversible and Cycle-Stable Lithium/Sodium Storage

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Energy & Environmental materials 2024年第4期7卷 135-142页

作者： Deliang Cheng Wenbiao Zhang Yi Tang Qingsheng Gao Renzong Hu Lichun Yang Min Zhu Institute of Advanced Materials Jiangxi Normal UniversityNanchang 330022China School of Materials Science and Engineering Guangdong Provincial Key Laboratory of Advanced Energy Storage MaterialsSouth China University of TechnologyGuangzhou 510641China College of Chemistry and Materials Science Guangdong Provincial Key Laboratory of Functional Supramolecular Coordination Materials and ApplicationsJinan UniversityGuangzhou 510632China Department of Chemistry Shanghai Key Laboratory of Molecular Catalysis and Innovative MaterialsLaboratory of Advanced Materials and Collaborative Innovation Center of Chemistry for Energy MaterialsFudan UniversityShanghai 200433China

SnO_(2),with its high theoretical capacity,abundant resources,and environmental friendliness,is widely regarded as a potential anode material for lithium-ion batteries(LIBs).Nevertheless,the coarsening of the Sn nanoparticles impedes the reconversion back to SnO_(2),resulting in low coulombic efficiency and rapid capacity *** this study,we fabricated a heterostructure by combining SnO_(2)nanoparticles with MoS_(2)nanosheets via plasma-assisted *** heterostructure consists of in-situ exfoliated MoS_(2)nanosheets predominantly in 1 T phase,which tightly encase the SnO_(2)nanoparticles through strong *** configuration effectively mitigates the volume change and particle aggregation upon ***,the strong affinity of Mo,which is the lithiation product of MoS_(2),toward Sn plays a pivotal role in inhibiting the coarsening of Sn nanograins,thus enhancing the reversibility of Sn to SnO_(2)upon ***,the SnO_(2)/MoS_(2)heterostructure exhibits superb performance as an anode material for LIBs,demonstrating high capacity,rapid rate capability,and extended ***,discharged/charged at a rate of 0.2 A g^(-1)for 300 cycles,it achieves a remarkable reversible capacity of 1173.4 mAh g^(-1).Even cycled at high rates of 1.0 and 5.0 A g^(-1)for 800 cycles,it still retains high reversible capacities of 1005.3 and 768.8 mAh g^(-1),***,the heterostructure exhibits outstanding electrochemical performance in both full LIBs and sodium-ion batteries.

关键词： 1 T-MoS_(2) heterostructure lithium-ion batteries Sn coarsening SnO_(2)

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Heterophase junction engineering-induced Co spin-state modulation of CoSe_(2) for large-current hydrogen evolution reaction

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Rare Metals 2024年第6期43卷 2660-2670页

作者： Bao-Chai Xu Ya-Ping Miao Min-Qin Mao Dong-Lian Li Song Xie Wei-Hong Jin Shu Xiao Jing Wen Zaenab Abd-Allah Zhi-Tian Liu Xiang Peng Paul K.Chu Hubei Key Laboratory of Plasma Chemistry and Advanced Materials School of Materials Science and EngineeringWuhan Institute of TechnologyWuhan 430205China School of Textile Science and Engineering Xi'an Polytechnic UniversityXi'an 710048China Institute of Advanced Wear and Corrosion Resistant and Functional Materials Jinan UniversityGuangzhou 510632China Institute of Safety Science and Engineering South China University of TechnologyGuangzhou 510641China Department of Engineering Manchester Metropolitan UniversityManchester M156BHUK Department of Physics Department of Materials Science and Engineeringand Department of Biomedical EngineeringCity University of Hong KongHong Kong 999077China

Efficient electrocatalysts are vital to large-current hydrogen production in commercial water splitting for green energy ***,a novel heterophase engineering strategy is described to produce polymorphic CoSe_(2)*** composition of the electrocatalysts consisting of both cubic CoSe_(2)(c-CoSe_(2))and orthorhombic CoSe_(2)(o-CoSe_(2))phases can be controlled *** results demonstrate that junction-induced spin-state modulation of Co atoms enhances the adsorption of intermediates and accelerates charge transfer resulting in superior large-current hydrogen evolution reaction(HER)***,the CoSe_(2)based heterophase catalyst with the optimal c-CoSe_(2)content requires an overpotential of merely 240 mV to achieve 1,000 mA·cm^(-2)as well as a Tafel slope of 50.4 mV·dec^(-1).Furthermore,the electrocatalyst can maintain a large current density of 1,500 mA·cm^(-2)for over 320 h without *** results reveal the advantages and potential of heterophase junction engineering pertaining to design and fabrication of low-cost transition metal catalysts for large-current water splitting.

关键词： Heterophase junction Spin-state Hydrogen evolution reaction Large current electrochemical hydrogen production Water splitting

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Unveiling the size effect of nitrogen-doped carbon-supported copper-based catalysts on nitrate-to-ammonia electroreduction

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Nano Research 2024年第4期17卷 2438-2443页

作者： Ran Li Taotao Gao Wenxi Qiu Minghao Xie Zhaoyu Jin Panpan Li College of Materials Science and Engineering Sichuan UniversityChengdu 610065China Institute for Advanced Study Chengdu UniversityChengdu 610106China Materials Science and Engineering Program and Walker Department of Mechanical Engineering The University of Texas at AustinAustinTexas 78712USA Institute of Fundamental and Frontier Sciences University of Electronic Science and Technology of ChinaChengdu 610054China

The electrocatalytic nitrate reduction reaction(NitRR)represents a promising approach toward achieving economically and environmentally sustainable ***,it remains a challenge to regulate the size effect of electrocatalysts to optimize the catalytic activity and ammonia ***,the Cu-based catalysts were tailored at the atomic level to exhibit a size gradient ranging from single-atom catalysts(SACs,0.15–0.35 nm)to single-cluster catalysts(SCCs,1.0–2.8 nm)and nanoparticles(NPs,20–30 nm),with the aim of studying the size effect for the NO_(3)^(-)-to-NH_(3) reduction ***,the Cu SCCs exhibit enhanced metal–substrate and metal–metal interactions by taking advantageous features of Cu SACs and Cu ***,Cu SCCs achieve exceptional electrocatalytic performance for the NitRR with a maximum Faradaic efficiency of ca.96%NH_(3)and the largest yield rate of ca.1.99 mg·h^(-1)·cm^(-2) at-0.5 V *** hydrogen electrode(RHE).The theoretical calculation further reveals the size effect and coordination environment on the high catalytic activity and selectivity for the *** work provides a promising various size-controlled design strategy for aerogel-based catalysts effectively applied in various electrocatalytic reactions.

关键词： nitrate electroreduction ammonia electrosynthesis size effect single-cluster catalyst

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Dual nanoprecipitation and nanoscale chemical heterogeneity in a secondary hardening steel for ultrahigh strength and large uniform elongation

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Journal of materials science & technology 2024年第18期185卷 245-258页

作者： Shidong Wang Jinhua Wang Shijie Zhang Daixiu Wei Yang Chen Xuequan Rong Wu Gong Stefanus Harjo Xiaochun Liu Zengbao Jiao Zhigang Yang Gang Sha Chunxu Wang Guang Chen Hao Chen Key Laboratory for Advanced Materials of Ministry of Education School of Materials Science and EngineeringTsinghua UniversityBeijing 100084China School of Materials Science and Engineering/Herbert Gleiter Institute of Nanoscience Nanjing University of Science and TechnologyNanjing 210094China National Key Laboratory of Advanced Casting Technologies MIIT Key Laboratory of Advanced Metallic and Intermetallic Materials TechnologyEngineering Research Center of Materials Behavior and DesignMinistry of EducationNanjing University of Science and TechnologyNanjing 210094China J-PARC Center Japan Atomic Energy AgencyIbaraki 319-1195Japan Institute of Metals College of Materials Science and EngineeringChangsha University of Science&TechnologyChangsha 410114China Department of Mechanical Engineering Research Institute for Advanced ManufacturingThe Hong Kong Polytechnic UniversityHong Kong 999077China Central Iron and Steel Research Institute Beijing 100081China

Nanoprecipitates and nanoscale retained austenite(RA)with suitable stability play crucial roles in deter-mining the yield strength(YS)and ductility of ultrahigh strength steels(UHSSs).However,owing to the kinetics incompatibility between nanoprecipitation and austenite reversion,it is highly challenging to si-multaneously introduce high-density nanoprecipitates and optimized RA in *** this work,through the combination of austenite reversion treatment(ART)and subsequent flash austenitizing(FA),nanoscale chemical heterogeneity was successfully introduced into a low-cost UHSS prior to the aging *** chemical heterogeneity involved the enrichment of Mn and Ni in the austenite *** resulting UHSS exhibited dual-nanoprecipitation of Ni(Al,Mn)and(Mo,Cr)_(2)C and nanoscale austenite stabilized via Mn and Ni *** hard martensitic matrix strengthened by high-density dual-nanoprecipitates con-strains the plastic deformation of soft RA with a relatively low fraction of-15%,and the presence of relatively stable nanoscale RA with adequate Mn and Ni enrichment leads to a marginal loss in YS but keeps a persistent transformation-induced plasticity(TRIP)*** a result,the newly-developed UHSS exhibits an ultrahigh YS of-1.7 GPa,an ultimate tensile strength(UTS)of-1.8 GPa,a large uniform elongation(UE)of-8.5%,and a total elongation(TE)of-13%.The strategy of presetting chemical heterogeneity to introduce proper metastable phases before aging can be extended to other UHSSs and precipitation-hardened alloys.

关键词： Ultrahigh strength steels Dual-nanoprecipitation Austenite stability TRIP effect Phase transformation

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Stretchable polymer composites with ultrahigh piezoelectric performance

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National science Review 2023年第8期10卷 203-210页

作者： Tongxiang Tang Zhonghui Shen Jian Wang Shiqi Xu Jiaxi Jiang Jiahui Chang Mengfan Guo Youjun Fan Yao Xiao Zhihao Dong Houbing Huang Xiaoyan Li Yihui Zhang Danyang Wang Long-Qing Chen Ke Wang Shujun Zhang Ce-Wen Nan Yang Shen State Key Lab of New Ceramics and Fine Processing School of Materials Science and Engineering Tsinghua University State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Center of Smart Materials and Devices Wuhan University of Technology Advanced Research Institute of Multidisciplinary Science Beijing Institute of Technology Applied Mechanics Laboratory Department of Engineering Mechanics Tsinghua University Center for Flexible Electronics Technology Tsinghua University School of Materials Science and Engineering University of New South Wales Department of Materials Science and Engineering The Pennsylvania State University State College Institute for Superconducting and Electronic Materials Australian Institute for Innovative MaterialsUniversity of Wollongong

Flexible piezoelectric materials capable of withstanding large deformation play key roles in flexible electronics. Ferroelectric ceramics with a high piezoelectric coefficient are inherently brittle, whereas polar polymers exhibit a low piezoelectric coefficient. Here we report a highly stretchable/compressible piezoelectric composite composed of ferroelectric ceramic skeleton, elastomer matrix and relaxor ferroelectric-based hybrid at the ceramic/matrix interface as dielectric transition layers, exhibiting a giant piezoelectric coefficient of 250 picometers per volt, high electromechanical coupling factor keff of 65%,ultralow acoustic impedance of 3MRyl and high cyclic stability under 50% compression strain. The superior flexibility and piezoelectric properties are attributed to the electric polarization and mechanical load transfer paths formed by the ceramic skeleton, and dielectric mismatch mitigation between ceramic fillers and elastomer matrix by the dielectric transition layer. The synergistic fusion of ultrahigh piezoelectric properties and superior flexibility in these polymer composites is expected to drive emerging applications in flexible smart electronics.

关键词： polymer composites piezoelectric materials structure design flexible electronics

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