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Construction of dendritic Pt–Pd bimetallic nanotubular heterostructure for advanced oxygen reduction

Interdisciplinary materials 2024年第6期3卷 907-918页

作者： Mingwei Wang Zhiyi Hu Jieheng Lv Zhiwen Yin Zhewei Xu Jingfeng Liu Shihao Feng Xiaoqian Wang Jiazhen He Sicheng Luo Dafu Zhao Hang Li Xuemin Luo Qi Liu Damin Liu Baolian Su Dongyuan Zhao Yong Liu International School of Materials Science and Engineering(ISMSE) State Key Laboratory of Advanced Technology for Materials Synthesis and ProcessingWuhan University of TechnologyWuhanChina Department of Chemistry Laboratory of Inorganic Materials ChemistryUniversity of NamurNamurBelgium Department of Chemistry Laboratory of Advanced MaterialsShanghai Key Lab of Molecular Catalysis and Innovative MaterialsState Key Laboratory of Molecular Engineering of PolymersFudan UniversityShanghaiChina

Compositions and morphologies of Pt-based electrocatalysts have great impact on the electrocatalytic activity and stability of oxygen reduction reaction(ORR).Herein,we report a novel design of one-dimensional(1D)Pt-Pd dendritic nanotubular heterostructures(DTHs)by controlling the degree of Pt 2+-Pt reduction reaction and Pd-Pt galvanic replacement reaction with uniform Pd nanowires as sacrificial *** obtained Pt-Pd bimetallic DTHs catalyst exhibited uniform and dense Pt dendritic nanobranches on the surface of 1D hollow Pt-Pd alloy nanotubes,possessing superior catalytic activity for ORR compared to state-of-the-art commercial Pt/C ***,the Pt_(4)Pd DTHs catalyst showed efficient mass activity(MA,1.05 A mg_(Pt)^(−1))and specific activity(SA,1.25 mA cm_(Pt)^(−2))at 0.9 V(***),and the catalyst exhibited high stability with 90.4%MA retention after 20000 potential *** Pt-Pd bimetallic DTHs configuration combines the advantages of 1D hollow nanostructures and dense Pt dendritic nanobranches,which results in rich electrochemical active surface sites,fast charge transport,and multiple dendritic anchoring points contact on carbon support,thus boosting its catalytic activity and stability towards electrocatalysis.

关键词： dendritic hollow heterostructures electrocatalysis one-dimensional nanowires oxygen reduction proton exchange membrane fuel cells

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A flame-retardant binder with high polysulfide affinity for safe and stable lithium–sulfur batteries

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Science China Chemistry 2024年第3期67卷 1028-1036页

作者： Guowei Yu Guofeng Ye Cheng Wang Chenyang Wang Zhaoyun Wang Pu Hu Yu Li Xi-Xi Feng Shuang-Jie Tan Min Yan Sen Xin Zhitian Liu Hubei Key Laboratory of Plasma Chemistry and Advanced Materials Hubei Engineering Technology Research Center of Optoelectronic and New Energy MaterialsSchool of Materials Science and EngineeringWuhan Institute of TechnologyWuhan 430205China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China CAS Key Laboratory of Molecular Nanostructure and Nanotechnology CAS Research/Education Center for Excellence in Molecular SciencesBeijing National Laboratory for Molecular Sciences(BNLMS)Institute of ChemistryChinese Academy of Sciences(CAS)Beijing 100190China University of Chinese Academy of Sciences Beijing 100049China

Lithium-sulfur(Li-S) batteries have shown promises for the next-generation, high-energy electrochemical storage, yet are hindered by rapid performance decay due to the polysulfide shuttle in the cathode and safety concerns about potential thermal runaway. To address the above challenges, herein, we show a flame-retardant cathode binder that simultaneously improves the electrochemical stability and safety of batteries. The combination of soft and hard segments in the polymer framework of binders allows high flexibility and mechanical strength for adapting to the drastic volume change during the Li(de)intercalation of the S cathode. The binder contains a large number of polar groups, which show the high affinity to polysulfides so that they help to anchor active S species at the cathode. These polar groups also help to regulate and facilitate the Li-ion transport, promoting the kinetics of polysulfide conversion reaction. The binder contains abundant phosphine oxide groups, which, in the case of battery's thermal runaway, decompose and release PO· radicals to quench the combustion reactions and stop the fire. Consequently, Li-S batteries using the new cathode binder show the improved electrochemical performance, including a low-capacity decay of 0.046% per cycle for 800 cycles at 1 C and favorable rate capabilities of up to 3 C. This work offers new insights on the practical realization of high-energy rechargeable batteries with stable storage electrochemistry and high safety.

关键词： lithium–sulfur battery polymer binder polysulfide affinity flame retardancy

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AI-driven material discovery for energy, catalysis and sustainability

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National Science Review 2025年第5期 77-78页

作者： Ning Han Bao-Lian Su Department of Electrical and Computer Engineering University of Toronto Laboratory of Inorganic Materials Chemistry(CMI) University of Namur State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology

Artificial intelligence (AI) is revolutionizing various sectors, including science,technology, industry and daily life [1,2].One key area where AI can make a significant impact is in material design, crucial for advan...

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Exploring the Magnetism of C_(5)/C_(2)B_(3) Heteroleptic Organolanthanide Sandwiches

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Chinese Journal of Chemistry 2025年第2期43卷 131-138页

作者： Ye-Ye Liu Qian-Cheng Luo Peng-Bo Jin Yan-Zhen Zheng Frontier Institute of Science and Technology(FIST) State Key Laboratory of Electrical Insulation and Power EquipmentMOE Key Laboratory for Nonequilibrium Synthesis and Modulation of Condensed MatterXi’an Key Laboratory of Electronic Devices and Material Chemistry and School of ChemistryXi’an Jiaotong UniversityXi’anShaanxi710054 China Department of Hepatobiliary Surgery and Institute of Advanced Surgical Technology and Engineering The First Affiliated Hospital of Xi’an Jiaotong UniversityXi’anShaanxi710061 China

Two families of cyclopentadienyl(Cp)/carboranyl heteroleptic sandwiched organolanthanide complexes,namely[Ln{η^(5):σ-Me_(2)C(C_(5)H_(4))(C_(2)B_(10)H_(10))}_(2)][Li(DME)_(3)](1Ln,Ln=Tb,Dy,Ho,Er)and[2-THF-2'-(μ^(2)-Cl)Li(THF)_"(3)-2,2'-Ln(nido-1,7-C_(2)B_(9)H_(11))Cp*](2Dy),were *** of 1Ln has been proposed based on the mixing-ligands idea by linking Cp and ***,the carborane cage of[Me_(2)C(C_(5)H_(4))(C_(2)B_(10)H_(10))]_(2)−deprotons and forms a mono-C−anion rather than deboron to form dicarborllide ***,the family of 1Ln features a dysprosocenium skeleton with extra two coordination of C−anions of *** coordination geometry is more like a tetrahedron if abstracting the centroids of two coordinated Cp *** this cubic-type geometry,no significant magnetic axiality is presented;only 1Dy and 1Tb show field-induced slow magnetic relaxation behavior below 10 *** by 1Ln,the free pentamethylcyclopentadienyl(Cp^(*−))and nido-dicarborllide ligands are used to sandwich central Dy3+ion,achieving heteroleptic complex *** bending angle by linking the centroid of Cp^(*−),Dy^(3+)and C_(2)B_(3)^(2−)in 2Dy is increased to 132.8(1)°.As such,the effective energy barrier for magnetic reversal(Ueff)and magnetic blocking temperature TB(ZFC)are both increased(Ueff=616(10)K;TB=6 K).The effort of further enhancing Ueff and TB in such heteroleptic organolanthanide sandwiches should rely on keeping increasing the ligand axiality.

关键词： Single-molecule magnets Heteroleptic sandwiched complexes nido-Dicarborllide Lanthanides Cyclopentadienyl

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Reduced graphene oxide-induced in-situ uniform growth of hydrated WO_(3) film for enhanced electrochromic performance

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Nano Research 2025年第4期18卷 569-577页

作者： Rui Fang Yang Liu Chunyu Shi Huihui Jin Zibo Chen Haohao Sun Ben Lv Daping He Xusheng Zheng Yuli Xiong State Key Laboratory of Advanced Technology for Materials Synthesis and Processing School of Materials Science and EngineeringWuhan University of TechnologyWuhan 430070China School of Science Wuhan University of TechnologyWuhan 430070China National Synchrotron Radiation Laboratory University of Science and Technology of ChinaHefei 230029China Sanya Science and Education Innovation Park of Wuhan University of Technology Sanya 572000China School of Materials Science and Engineering Wuhan University of TechnologyWuhan 430070China

WO_(3)-graphene electrochromic materials are widely used in electrochromic devices including smart windows and electronic displays,due to their ability to adjust optical transmittance in the visible and near-infrared ranges under low electrode ***,the uniformity of the film remains a challenge for the widely used physical mixing-coating *** this study,we present a two-dimensional material-assisted synthesis of a porous hydrated WO_(3) film(WH-rGO)based on reduced graphene oxide(rGO)nanosheets and WO_(3)(rGO-WO_(3))seed layer via a hydrothermal *** incorporation of rGO not only promotes the uniform growth of hydrated WO_(3) film,enhancing ion transport but also introduces oxygen vacancies,creating an efficient conduction pathway for charge *** resulting WH-rGO film exhibits impressive performance,achieving 71% optical modulation at 700 nm,with bleaching and coloring times of 4.2 and 1.0 *** coloration efficiency is calculated at 156.11 cm^(2)·C^(-1),and the optical modulation is maintained at 93% of the initial optical modulation after 1000 cycles applied in the +1.0 and -1.1 V potential *** work offers new insights into the role of oxygen vacancies in enhancing the electrochromic properties of hydrated WO_(3) films through the addition of *** also provides a promising approach for the synthesis of electrochromic materials,facilitating their application in smart window technologies.

关键词： electrochromic film hydrated tungsten oxide reduced graphene oxide oxygen vacancy

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Achieving asymmetric redox chemistry for oxygen evolution reaction through strong metal-support interactions

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Journal of Energy Chemistry 2024年第9期96卷 526-535页

作者： Shihao Wang Meiling Fan Hongfei Pan Jiahui Lyu Jinsong Wu Haolin Tang Haining Zhang State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070HubeiChina National Energy Key Laboratory for New Hydrogen-Ammonia Energy Technologies Foshan Xianhu LaboratoryFoshan 528200GuangdongChina International School of Materials Science and Engineering(School of Materials and Microelectronics) Wuhan University of TechnologyWuhan 430070HubeiChina Nanostructure Research Centre Wuhan University of TechnologyWuhan 430070HubeiChina Hubei Key Laboratory of Fuel Cell Wuhan University of TechnologyWuhan 430070HubeiChina

Water electrolysis poses a significant challenge for balancing catalytic activity and stability of oxygen evolution reaction(OER)*** this study,we address this challenge by constructing asymmetric redox chemistry through elaborate surface OO–Ru–OH and bulk Ru–O–Ni/Fe coordination moieties within single-atom Ru-decorated defective NiFe LDH nanosheets(Ru@d-NiFe LDH)in conjunction with strong metal-support interactions(SMSI).Rigorous spectroscopic characterization and theoretical calculations indicate that single-atom Ru can delocalize the O 2p electrons on the surface and optimize d-electron configurations of metal atoms in bulk through ***^(18)O isotope labeling experiment based on operando differential electrochemical mass spectrometry(DEMS),chemical probe experiments,and theoretical calculations confirm the encouraged surface lattice oxygen,stabilized bulk lattice oxygen,and enhanced adsorption of oxygen-containing intermediates for bulk metals in Ru@d-NiFe LDH,leading to asymmetric redox chemistry for *** Ru@d-NiFe LDH electrocatalyst exhibits exceptional performance with an overpotential of 230 mV to achieve 10 mA cm^(−2)and maintains high robustness under industrial current *** approach for achieving asymmetric redox chemistry through SMSI presents a new avenue for developing high-performance electrocatalysts and instills confidence in its industrial applicability.

关键词： Reaction redox chemistry Strong metal-support interactions Layered double hydroxides Electrocatalysts Water electrolysis

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Design and Dynamic Experiment of Al-Cu Graded materials Impactor with Strain Rate of 10^(4)–10^(5)/s

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稀有金属材料与工程 2025年第3期54卷 581-586页

作者： Hu Jianian Zhou Zizheng Li Yidi Chen Xiang Yang Gang Liu Jintao Zhang Jian State Key Laboratory of Precision Blasting Jianghan UniversityWuhan 430056China Hubei Key Laboratory of Blasting Engineering Jianghan UniversityWuhan 430056China Luoyang Ship Material Research Institute Luoyang 471023China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China

Based on simplified calculations of one-dimensional wave systems,loading pressure platform curves of Al-Cu gradient materials(GMs)impactor were *** Al-Cu GMs were prepared using tape-pressing sintering,and their acoustic properties were characterized to match the design *** parallelism of the Al-Cu GM was confirmed using a three-dimensional surface profilometry machine.A one-stage light-gas gun was used to launch the Al-Cu GM,impacting an Al-LiF target at a velocity of 400 m/*** results of the experimental strain rate demonstrate that the Al-Cu GMs can realize the precise control of the strain rate within the range of 10^(4)‒10^(5)/s in the high-speed impact experiments.

关键词： high strain rate Al-Cu graded materials impactor acoustic impedance gas gun experiment

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Microemulsion synthesis of Mesoporous β-tricalcium Phosphate Powder with a Novel System

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Journal of Wuhan University of technology(materials Science) 2022年第4期37卷 773-778页

作者： BIELEC Monikaq HUANG An XIA Yuhao DAI Honglian State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyShenzhen 5180ooChina Shenzhen Institute of Wuhan University of Technology Wuhan 430070China

The synthesis of mesoporous β-tricalcium phosphate(β-TCP)powder was performed by using the microemulsion approach,with hexadecyltrimethyl ammonium bromide(CTAB)/cyclohexane/n-octyl alcohol microemulsion *** influences of different pH values and calcination temperatures on the phase composition of the β-TCP powder were *** in vitro proliferation of bone marrow mesenchymal stem cells(BMSCs)in the suspensions of β-TCP powders with meso-structure was *** phase composition,mesoporous structure,powder morphology,cell morphology and the optical density(OD)were characterized through X-ray diffraction(XRD),field emission scanning electron microscopy(FESEM),Fourier transform infrared(FTIR)spectroscopy,Nadsorption-desorption isotherms,inverted phase contrast microscopy and Multiskan spectrum,*** mesoporous β-TCP powder with specific surface area of 12.85 m^(2)/g and the average pore size 7.11 nm was obtained through the microemulsion approach(100 g/L CTAB/250 mL/L cyclohexane/250 mL/L n-octyl alcohol)with a controlled pH of 7.0,after calcinating the powder at 800℃.It was confirmed that mesoporous β-TCP powder benefits the activity of BMSCs more than the non-mesoporous β-TCP powder.

关键词： β-tricalcium phosphate mesoporous microemulsion bone marrow mesenchymal stem cells

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Constructing electron-blocking grain boundaries in garnet to suppress lithium dendrite growth

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Journal of advanced Ceramics 2024年第2期13卷 166-175页

作者： Xing Xiang Zecheng Fang Congkun Du Zhenzhen Zhao Jiajia Chen Yanhua Zhang Huihu Wang Chenhuinan Wei Fei Chen Qiang Shen Hubei Provincial Key Laboratory of Green Materials for Light Industry Hubei University of TechnologyWuhan 430068China Hubei Longzhong Laboratory Wuhan University of Technology Xiangyang Demonstration ZoneXiangyang 441000China Collaborative Innovation Center of Green Light-weight Materials and Processing Hubei University of TechnologyWuhan 430068China New Materials and Green Manufacturing Talent Introduction and Innovation Demonstration Base Hubei University of TechnologyWuhan 430068China State Key Lab of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China

Li_(7)La_(3)Zr_(2)O_(12)(LLZO)is considered as a promising solid-state electrolyte due to its high ionic conductivity,wide electrochemical window,and excellent electrochemical ***,its application in solid-state lithium metal batteries(SSLMBs)is impeded by the growth of lithium dendrites in LLZO due to some reasons such as its high electronic *** this study,lithium fluoride(LiF)was introduced into Ta-doped LLZO(LLZTO)to modify its grain boundaries to enhance the performance of SSLMBs.A nanoscale LiF layer was uniformly coated on the LLZTO grains,creating a threedimensional continuous electron-blocking network at the grain *** from the electronic insulator LiF and the special structure of the modified LLZTO,the symmetric cells based on LLZO achieved a high critical current density(CCD)of 1.1 mA·cm^(-2)(in capacity-constant mode)and maintained stability over 2000 h at 0.3 mA·cm^(-2).Moreover,the full cells combined with a LiFePO_(4)(LFP)cathode,demonstrated excellent cycling performance,retaining 97.1% of capacity retention after 500 cycles at 0.5 ***,this work provides a facile and effective approach for preparing a modified electrolyte suitable for high-performance SSLMBs.

关键词： solid electrolyte garnet lithium dendrite microstructure solid-state batteries

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Accelerated ion/electron transport kinetics and increased active sites via local internal electric fields in heterostructured VO_(2)–carbon cloth for enhanced zinc-ion storage

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Nano Research 2023年第1期16卷 503-512页

作者： Ping Luo Wenwei Zhang Wanyue Cai Zhen Huang Gangyuan Liu Chang Liu Shiyu Wang Feng Chen Lixue Xia Yan Zhao Shijie Dong Lu Xia Hubei Provincial Key Laboratory of Green Materials for Light Industry Hubei Engineering Laboratory of Automotive Lightweight Materials and ProcessingNew Materials and Green Manufacturing Talent Introduction and Innovation Demonstration Base School of Materials and Chemical EngineeringHubei University of TechnologyWuhan 430068China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China State Key Laboratory of Silicate Materials for Architectures International School of Materials Science and EngineeringWuhan University of TechnologyWuhan 430070China Wuhan Polytechnic University Wuhan 430023China

Although the performance of the self-standing electrode has been enhanced for aqueous zinc-ion batteries(AZIBs),it is necessary to explore and analyse the deep modification mechanism(especially interface effects).Herein,density functional theory(DFT)calculations are applied to investigate the high-performance cathode based on the VO_(2)/carbon cloth composites with heterostructures interface(H-VO_(2)@CC).The adsorption energy comparisons and electron structure analyses verify that HVO_(2)@CC has extra activated sites at the interface,enhanced electrical conductivity,and structural stability for achieving highperformance AZIBs due to the presence of built-in electric field at the ***,the designed self-standing HVO_(2)@CC cathode delivers higher rate capacity,longer-life cyclability,and faster electronic/ion transmission kinetics benefiting from the synergistic *** risks of active material shedding and dissolution during the dis/charge process of two cathodes were evaluated via ex-situ ultraviolet–visible(UV–vis)spectrum and inductively coupled plasma-atomic emission spectroscopy(ICP-AES)***,this investigation also explores the charge storage mechanism of H-VO_(2)@CC through various exsitu and in-situ characterization *** finding can shed light on the significant potential of heterostructures interface engineering in practical applications and provide a valuable direction for the development of cathode materials for AZIBs and other metal-ion batteries.

关键词： aqueous zinc ion battery heterostructures interface built-in electric field VO_(2)(B) density functional theory

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