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Growth of magnetic metals on carbon microspheres with synergetic dissipation abilities to broaden microwave absorption

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Journal of materials Science & technology 2022年第12期107卷 100-110页

作者： Biao Zhao Yang Li Qingwen Zeng Bingbing Fan Lei Wang Rui Zhang Renchao Che Laboratory of Advanced Materials Shanghai Key Lab of Molecular Catalysis and Innovative MaterialsFudan UniversityShanghai 200438China Department of Materials Science Fudan UniversityShanghai 200438China Henan Key Laboratory of Aeronautical Materials and Application Technology School of Material Science and EngineeringZhengzhou University of AeronauticsZhengzhouHenan 450046China School of Material Science and Engineering Zhengzhou UniversityZhengzhouHenan 450001China State Key Laboratory of Solidification Processing Northwestern Polytechnical UniversityXi’an 710072China

Microwave absorption(MA) materials have been captured extensive attentions due to the serious electromagnetic(EM) pollution. Numerous interests focus on the MA performances of core-shell structural composites with magnetic constituents as cores and dielectric constituents as shells, which inevitably suppressed the magnetic coupling causing the decrease of magnetic loss to some extent. Herein, the coreshell structural carbon(C) microsphere/magnetic metal composites were fabricated through the combination of an electrostatic assembly approach and subsequent in-situ reduction reaction. The complex permittivity and permeability of core-shell C@magnetic metal composite system can be effective adjusted by the constituent and microstructure of shells. Thanks to the distinct magnetic coupling from the subtle designed structures and the promotion of the magnetic-dielectric synergy, the C@magnetic metal composite exhibited enhanced MA properties. The optimal reflection loss(RL) of C@Ni composite was-54.1 dB with a thickness of 3.4 mm, meanwhile the effective absorbing band could reach over 5.5 GHz at only a1.8 mm thickness. Broad absorption bandwidth with RL below-10 d B could achieve 6.0 GHz and 6.7 GHz for C@Co and C@Ni Co composites with a thin 2.1 mm thickness, respectively. Our exciting findings might lead a guide on the novel structure design for the functional core-shell structural composites used for microwave absorption.

关键词： Microwave absorption Core-shell structure C@magnetic metal composite Interfacial polarization Magnetic coupling

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Single-cell yolk-shell nanoencapsulation for long-term viability with size-dependent permeability and molecular recognition

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国家科学评论（英文版） 2021年第4期8卷 120-136页

作者： Li Wang Yu Li Xiao-Yu Yang Bo-Bo Zhang N(o)elle Ninane Henk J.Busscher Zhi-Yi Hu Cyrille Delneuville Nan Jiang Hao Xie Gustaaf Van Tendeloo Tawfique Hasan Bao-Lian Su State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430070 China Laboratory of Inorganic Materials Chemistry (CMI) University of Namur Namur B-5000 Belgium State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430070 China Laboratory of Inorganic Materials Chemistry (CMI) University of Namur Namur B-5000 Belgium Namur Research Institute for Life Sciences (Narilis) University of Namur Namur B-5000 Belgium Department of Biomedical Engineering University of Groningen and University Medical Centre Groningen Groningen 9713 AV The Netherlands State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430070 China Nanostructure Research Centre (NRC) Wuhan University of Technology Wuhan 430070 China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430070 China School of Engineering and Applied Sciences Harvard University Cambridge MA 02138 USA Nanostructure Research Centre (NRC) Wuhan University of Technology Wuhan 430070 China Electron Microscopy for Materials Science (EMAT) University of Antwerp Antwerp B-2020 Belgium Cambridge Graphene Centre University of Cambridge Cambridge CB3 0FA UK

Like nanomaterials,bacteria have been unknowingly used for *** hold significant economic potential for fuel and medicinal compound *** full exploitation,however,is impeded by low biological activity and stability in industrial *** cellular encapsulation addresses these limitations,cell survival is usually compromised due to shell-to-cell contacts and low ***,we report ordered packing of silica nanocolloids with organized,uniform and tunable nanoporosities for single cyanobacterium nanoencapsulation using protamine as an electrostatic template.A space between the capsule shell and the cell is created by controlled internalization ofprotamine,resulting in a highly ordered porous shell-void-cell structure *** unique yolk-shell nanostructures provide long-term cell viability with superior photosynthetic activities and resistance in harsh *** addition,engineering the colloidal packing allows tunable shell-pore diameter for size-dependent permeability and introduction of new functionalities for specific molecular *** strategy could significantly enhance the activity and stability of cyanobacteria for various nanobiotechnological applications.

关键词： cell surface engineering protein internalization ordered colloidal packing high photosynthetic ability harsh condition resistance thiol-functionalization

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Multimaterial additive manufacturing manipulator for fabricating magnetoelectric pressure sensors

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Science China(Technological Sciences) 2022年第11期65卷 2542-2550页

作者： LIU ZhuFeng LI ZhaoQing WANG Qi WANG Yan YANG Lei NIE Xiang GENG Peng WU ZhenHua TANG SiHan YANG Lei WU HongZhi SHI YunSong CHEN Peng SU Bin ZHANG LiChao YAN ChunZe SHI YuSheng State Key Laboratory of Materials Processing and Die&Mould Technology Huazhong University of Science and Technology Wuhan 430074China State Key Laboratory of Advanced Electromagnetic Engineering and Technology Huazhong University of Science and TechnologyWuhan 430074China Schol of Materials Science and Enginering Wuhan Insitute of TechnologyWuhan 430205Chinai School of Transportation and Logisis Engineering Wuhan University of TechnologyWuhan 430063China Deparment of Orthopaedics Union HospitalTongji Medical CollegeHuazhong University of Science and Technology Wuhan 430030China

The simultaneous placement of different types of materials including polymers,ceramics,and metals,in their desired positions could be adopted to manufacture end-use devices/apparatuses with diverse functionalities and significantly reduce the fabrication cost and ***,existing additive manufacturing(AM)approaches can only treat one material species at a time due to their intrinsic working *** we develop an AM manipulator for manufacturing a wide variety of material species,including polymers,ceramics,and metals,through a multifilament transport strategy assisted by laser *** six-jaw manipulator contains three pairs of filament delivering/cutting systems for transporting diverse materials and a beam of tunable laser as the thermal *** whole apparatus is integrated into a robotic manipulator to create a multifreedom manufacturing *** this innovation,products with multiple material species and desired complex geometries can be fabricated on ***,we synthesize a multimaterial(polymer/ceramic/metal)printed magnetoelectric pressure sensor that can convert applied mechanical forces to electricity and maintain efficiency even after undergoing 10000 cycles of pressure/*** this multimaterial filament transport and laser manufacturing strategy,our AM manipulator exhibits promising application in the advanced manufacturing of embedded electronics,sensors,soft robotics,and customizable medical devices.

关键词： multiple materials additive manufacturing laser manipulator magnetoelectric

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Ultra-High-Performance Aluminum-Based Hybrid Supercapacitors Prepared for Nitrogen-Doped Micro-Mesoporous Carbon Sphere

SSRN

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SSRN 2023年

作者： Sun, Weiyi Xing, Lingli Zhang, Bomian Shi, Wenchao Ren, Jingke Zhang, Xinyu Xiong, Fangyu An, Qinyou State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China Hubei Xiangyang441000 China

Aluminum-based devices are promising candidates for the next generation of energy storage due to the advantages of high energy density, high safety, and low cost. The aluminum ion batteries (AIBs) are based on the electrochemical intercalation/deintercalation reactions against the electrodes, but the selection of the cathode is limited to present. The cathode reactions of cation-type AIBs are plagued by the poor kinetics of solid-state diffusion from high charge density of Al3+ and anion-type AIBs show poor capacity due to the intercalation of large-sized chloroaluminate (AlCl4−) active ions into the cathode. Here, we deliberately adopted a hybrid capacitor-battery mechanism and employed a nitrogen-doped micro-mesoporous carbon sphere of a high specific area as the cathode and aluminum as the anode to construct an aluminum-based energy storage device. After optimization, it exhibits an excellent discharge capacity of 224 mA h g−1 at a current density of 300 mA g−1, and exceptional cycling performance with a discharge capacity as high as 114 mA h g−1 at 10 A g−1 after 35000 cycles. The ultra-high-performance aluminum-based hybrid supercapacitor (Al-HSC) may lead to a new direction for the development of aluminum-based energy storage devices. © 2023, The Authors. All rights reserved.

关键词： Aluminum

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Progress and perspectives in dielectric energy storage ceramics

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Journal of advanced Ceramics 2021年第4期10卷 675-703页

作者： Dongxu LI Xiaojun ZENG Zhipeng LI Zong-Yang SHEN Hua HAO Wenqin LUO Xingcai WANG Fusheng SONG Zhumei WANG Yueming LI Energy Storage and Conversion Ceramic Materials Engineering Laboratory of Jiangxi Province China National Light Industry Key Laboratory of Functional Ceramic MaterialsSchool of Materials Science and EngineeringJingdezhen Ceramic UniversityJingdezhen 333403China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing School of Materials Science and EngineeringWuhan University of TechnologyWuhan 430070China Chengdu Hongke Electronic Technology Co. Ltd.Chengdu 610000China

Dielectric ceramic capacitors,with the advantages of high power density,fast chargedischarge capability,excellent fatigue endurance,and good high temperature stability,have been acknowledged to be promising candidates for solid-state pulse power *** review investigates the energy storage performances of linear dielectric,relaxor ferroelectric,and antiferroelectric from the viewpoint of chemical modification,macro/microstructural design,and electrical property *** progress of ceramic bulks and films for Pb-based and/or Pb-free systems is ***,we propose the perspectives on the development of energy storage ceramics for pulse power capacitors in the future.

关键词： energy storage ceramics dielectric relaxor ferroelectric antiferroelectric pulse power capacitor

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Confined cobalt single-atom catalysts with strong electronic metal-support interactions based on a biomimetic self-assembly strategy

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Carbon Energy 2024年第9期6卷 156-171页

作者： Bowen Guo Zekun Wang Lei Zheng Guang Mo Hongjun Zhou Dan Luo State Key Laboratory of Heavy Oil Processing Beijing Key Laboratory of Biogas Upgrading UtilizationCollege of New Energy and MaterialsChina University of Petroleum(Beijing)BeijingChina Beijing Key Laboratory of Micro-Nano Energy and Sensor CAS Center for Excellence in NanoscienceBeijing Institute of Nanoenergy and NanosystemsChinese Academy of SciencesBeijingChina School of Chemical Engineering Shandong Institute of Petroleum and Chemical TechnologyDongyingShandongChina School of Chemistry Beijing Advanced Innovation Center for Biomedical EngineeringBeihang UniversityBeijingChina Institute of High Energy Physics Chinese Academy of SciencesBeijingChina

Designing high-performance and low-cost electrocatalysts for oxygen evolu-tion reaction(OER)is critical for the conversion and storage of sustainable energy *** by the biomineralization process,we utilized the phosphorylation sites of collagen molecules to combine with cobalt-based mononuclear precursors at the molecular level and built a three-dimensional(3D)porous hierarchical material through a bottom-up biomimetic self-assembly strategy to obtain single-atom catalysts confined on carbonized biomimetic self-assembled carriers(Co SACs/cBSC)after subsequent high-temperature *** this strategy,the biomolecule improved the anchoring efficiency of the metal precursor through precise functional groups;meanwhile,the binding-then-assembling strategy also effectively suppressed the nonspecific adsorption of metal ions,ultimately preventing atomic agglomeration and achieving strong electronic metal-support interactions(EMSIs).Experimental characterizations confirm that binding forms between cobalt metal and carbonized self-assembled substrate(Co–O_(4)–P).Theoretical calculations disclose that the local environment changes significantly tailored the Co d-band center,and optimized the binding energy of oxygenated intermediates and the energy barrier of oxygen *** a result,the obtained Co SACs/cBSC catalyst can achieve remarkable OER activity and 24 h durability in 1 M KOH(η_(10) at 288 mV;Tafel slope of 44 mV dec^(-1)),better than other transition metal-based catalysts and commercial IrO_(2).Overall,we presented a self-assembly strategy to prepare transition metal SACs with strong EMSIs,providing a new avenue for the preparation of efficient catalysts with fine atomic structures.

关键词： biomimetic self-assembly support electronic metal-support interactions oxygen evolution reaction single atoms catalysts

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Cobalt doping boosted electrocatalytic activity of CaMn3O6 for hydrogen evolution reaction

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Nano Research 2022年第4期15卷 2870-2876页

作者： Qun Li Kaisi Liu Siwei Gui Jiabin Wu Xiaogang Li Zaifang Li Hongrun Jin Hui Yang Zhimi Hu Wenxi Liang Liang Huang Wuhan National Laboratory for Optoelectronics Huazhong University of Science and TechnologyWuhan 430074China China-Australia Institute for Advanced Materials and Manufacturing Jiaxing UniversityJiaxing 314001China State Key Laboratory of Material Processing and Die&Mold Technology Department of MechanicsSchool of Aerospace EngineeringHuazhong University of Science and TechnologyWuhan 430074China

The development of earth-abundant-metal-based electrocatalysts with high efficiency and long-term stability for hydrogen evolution reaction(HER)is crucial for the clean and renewable energy ***,we report a molten-salt method to synthesize Co-doped CaMn_(3)O_(6)(CMO)nanowires(NWs)as effective electrocatalyst for *** as-obtained CaMn_(3-x)Co_(x)O_(6)(CMCO)exhibits a small onset overpotential of 70 mV,a required overpotential of 140 mV at a current density of 10 mA·cm^(-2),a Tafel slope of 39 mV·dec^(-1)in 0.1 M HClO_(4),and a satisfying long-term *** characterizations combined with density functional theory(DFT)calculations demonstrate that the obtained HER performance can be attributed to the Co-doping which altered CMO’s surface electronic structures and *** the simplicity of synthesis route and the abundance of the pertinent elements,the synthesized CMCO shows a promising prospect as a candidate for the development of earth-abundant,metal-based,and cost-effective electrocatalyst with superior HER *** results also establish a strategy of rational design and construction of novel electrocatalyst toward HER by tailoring band structures of transition metal oxides(TMOs).

关键词： CMCO nanowires hydrogen evolution reaction electronic structure dopant

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Designing polymer nanocomposites with high energy density using machine learning

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npj Computational materials 2021年第1期7卷 999-1007页

作者： Zhong-Hui Shen Zhi-Wei Bao Xiao-Xing Cheng Bao-Wen Li Han-Xing Liu Yang Shen Long-Qing Chen Xiao-Guang Li Ce-Wen Nan State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Center of Smart Materials and DevicesWuhan University of TechnologyWuhanChina International School of Materials Science and Engineering Wuhan University of TechnologyWuhanChina Hefei National Laboratory for Physical Sciences at the Microscale Department of Physics and CAS Key Laboratory of Strongly-Coupled Quantum Matter Physics University of Science and Technology of China HefeiChina Department of Materials Science and Engineering The Pennsylvania State UniversityUniversity ParkPAUnited States School of Materials Science and Engineering State Key Lab of New Ceramics and Fine ProcessingTsinghua UniversityBeijingChina

Addressing microstructure-property relations of polymer nanocomposites is vital for designing advanced dielectrics for electrostatic energy ***,we develop an integrated phase-field model to simulate the dielectric response,charge transport,and breakdown process of polymer ***,based on 6615 high-throughput calculation results,a machine learning strategy is schemed to evaluate the capability of energy *** find that parallel perovskite nanosheets prefer to block and then drive charges to migrate along with the interfaces in x-y plane,which could significantly improve the breakdown strength of polymer *** verify our predictions,we fabricate a polymer nanocomposite P(VDF-HFP)/Ca_(2)Nb_(3)O_(10),whose highest discharged energy density almost doubles to 35.9 J cm^(−3) compared with the pristine polymer,mainly benefit from the improved breakdown strength of 853 MVm^(−1).This work opens a horizon to exploit the great potential of 2D perovskite nanosheets for a wide range of applications of flexible dielectrics with the requirement of high voltage endurance.

关键词： polymer energy perovskite

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Phosphorus modulated porous CeO_(2)nanocrystallines for accelerated polysulfide catalysis in advanced Li-S batteries

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Journal of materials Science & technology 2022年第36期131卷 212-220页

作者： Xuefeng Tao Zhao Yang Menghao Cheng Rui Yan Fan Chen Sujiao Cao Shuang Li Tian Ma Chong Cheng Wei Yang College of Polymer Science and Engineering State Key Laboratory of Polymer Materials EngineeringSichuan UniversityChengdu 610065China State Key Laboratory of Advanced Processing and Recycling of Non-ferrous Metals Lanzhou University of TechnologyLanzhou 730050China Department of Ultrasound National Clinical Research Center for GeriatricsWest China HospitalSichuan UniversityChengdu 610041China

The insulating nature of sulfur species,sluggish reaction kinetics,and uncontrolled dissolution of lithium polysulfide(LiPS)intermediates during the complex and multiphase sulfur redox process,have severely inhibited the applications of Li-S *** this study,we report a rational strategy to accelerate the polysulfide catalysis via constructing phosphorus modulated porous CeO_(2)(P-CeO_(2))for advanced Li-S *** morphology and surface analysis demonstrate that the P-CeO_(2)consists of abundant Pmodulated porous CeO_(2)*** battery performance reveals that the introduction of P will lead to an improved initial capacity of 1027 mA hg^(-1)than that of bare CeO_(2)(895.7 mA hg^(-1))at 0.2 *** addition,the P-CeO_(2)cathode can maintain a low capacity decay ratio of 0.10%per cycle after 500 cycles at 1.0 *** coin battery tests suggest that the P-CeO_(2)cathode presents faster oxidation-reduction kinetics of LiPS and quick diffusion of Li^+***,the studies of redox processes and chemical interactions of LiPS have demonstrated the P-CeO_(2)cathode displays stronger adsorption of Li_(2)S_(6),higher redox peak current,and earlier precipitation of Li_(2)S than the bare CeO_(2).This study demonstrates for the first time that the P-modulation of metal oxide surface can simultaneously promote the catalytic reaction kinetics and chemical interaction of *** anticipate that this P-modulation method can be extended to many other nanostructured metal catalytic sites for developing affordable advanced Li-S batteries.

关键词： Metal oxides P-modulated porous CeO_(2) Polysulfide catalytic materials Shuttle effects Lithium-sulfur batteries

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Multi-functional layered double hydroxides supported by nanoporous gold toward overall hydrazine splitting

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Frontiers of Chemical Science and Engineering 2024年第1期18卷 61-69页

作者： Yongji Qin Huijie Cao Qian Liu Shaoqing Yang Xincai Feng Hao Wang Meiling Lian Dongxing Zhang Hua Wang Jun Luo Xijun Liu ShenSi Lab Shenzhen Institute for Advanced StudyUniversity of Electronic Science and Technology of ChinaShenzhen 518110China Institute for New Energy Materials and Low-Carbon Technologies School of Materials Science and EngineeringTianjin University of TechnologyTianjin 300384China State Key Laboratory of Featured Metal Materials and Life-cycle Safety for Composite Structures Guangxi Key Laboratory of Processing for Non-ferrous Metals and Featured MaterialsSchool of ResourcesEnvironment and MaterialsGuangxi UniversityNanning 530004China Institute for Advanced Study Chengdu UniversityChengdu 610106China China National Coal Group Corporation Beijing 100120China Tianjin Engineering Research Center of Civil Aviation Energy Environment and Green Development School of Transportation Science and EngineeringCivil Aviation University of ChinaTianjin 300300China

Layered double hydroxides have demonstrated great potential for the oxygen evolution reaction,which is a crucial half-reaction of overall water ***,it remains challenging to apply layered double hydroxides in other electrochemical reactions with high efficiency and ***,we report two-dimensional multifunctional layered double hydroxides derived from metalorganic framework sheet precursors supported by nanoporous gold with high porosity,which exhibit appealing performances toward oxygen/hydrogen evolution reactions,hydrazine oxidation reaction,and overall hydrazine *** as-prepared catalyst only requires an overpotential of 233 mV to reach 10 mA·cm^(-2) toward oxygen evolution *** overall hydrazine splitting cell only needs a cell voltage of 0.984 V to deliver 10 mA·cm^(-2),which is far more superior than that of the overall water splitting system(1.849 V).The appealing performances of the catalyst can be contributed to the synergistic effect between the metal components of the layered double hydroxides and the supporting effect of the nanoporous gold substrate,which could endow the sample with high surface area and excellent conductivity,resulting in superior activity and stability.

关键词： layered double hydroxide oxygen evolution reaction hydrazine oxidation reaction overall hydrazine splitting hydrogen production

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