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Rekindling hopes for lithium-sulfur batteries

National Science Review 2025年第4期 88-90页

作者： Hongtao Qu Bao-Lian Su Laboratory of Inorganic Materials Chemistry (CMI) University of Namur State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology

Lithium-sulfur(Li-S) batteries represent a promising solution for next-generation energy storage due to their high energy density, low cost, and environmental friendliness. However, liquid electrolytebased Li-S batteries are plagued by the‘polysulfide shuttling' effect, leading to severe performance degradation [1,2].

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Enhanced Electrical Properties of Bi_(2−x)Sb_(x)Te_(3) Nanoflake Thin Films Through Interface Engineering

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Energy & Environmental materials 2024年第6期7卷 359-366页

作者： Xudong Wu Junjie Ding Wenjun Cui Weixiao Lin Zefan Xue Zhi Yang Jiahui Liu Xiaolei Nie Wanting Zhu Gustaaf Van Tendeloo Xiahan Sang State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China NRC(Nanostructure Research Centre) Wuhan University of TechnologyWuhan 430070China EMAT(Electron Microscopy for Materials Science) University of AntwerpGroenenborgerlaan 171Antwerp 2023Belgium

The structure–property relationship at interfaces is difficult to probe for thermoelectric materials with a complex interfacial *** thermoelectric materials with a simple,structurally-uniform interface provides a facile way to understand how these interfaces influence the transport ***,we synthesized Bi_(2−x)Sb_(x)Te_(3)(x=0,0.1,0.2,0.4)nanoflakes using a hydrothermal method,and prepared Bi_(2−x)Sb_(x)Te_(3) thin films with predominantly(0001)interfaces by stacking the nanoflakes through spin *** influence of the annealing temperature and Sb content on the(0001)interface structure was systematically investigated at atomic scale using aberration-corrected scanning transmission electron *** and Sb doping facilitate atom diffusion and migration between adjacent nanoflakes along the(0001)*** such it enhances interfacial connectivity and improves the electrical transport *** reactions create new interfaces that increase the scattering and the Seebeck *** to the simultaneous optimization of electrical conductivity and Seebeck coefficient,the maximum power factor of the Bi_(1.8)Sb_(0.2)Te_(3) nanoflake films reaches 1.72 mW m^(−1)K^(−2),which is 43%higher than that of a pure Bi_(2)Te_(3) thin film.

关键词： Bi_(2)Te_(3) nanoflakes interface engineering scanning transmission electron microscopy thermoelectric thin film

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Enhanced Electrochemical Performances of Ni Doped Cr_(8)O_(21)Cathode materials for Lithium-ion Batteries

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Journal of Wuhan University of technology(materials Science) 2023年第6期38卷 1242-1247页

作者： TANG Guoli LIU Hanxing YU Zhiyong YANG Bo KONG Linghua School of Materials Science and Engineering Wuhan University of TechnologyWuhan 430070China International School of Materials Science and Engineering Wuhan University of TechnologyWuhan 430070China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan 430070China

Cathode materials,nickel doped Cr_(8)O_(21),were synthesized by a solid-state *** effects of Ni doping on the electrochemical performances of Cr_(8)O_(21) were *** experimental results show that the discharge capacities of the samples depend on the nickel contents,which increases firstly and then decreases with increasing Ni *** Ni_(0.5)Cr_(7.5)O_(21)delivers a first capacity up to 392.6 m Ah·g^(-1)at *** addition,Ni doped sample also demonstrates enhanced cycling stability and rate capability compared with that of the bare Cr_(8)O_(21).At 1 C,an initial discharge capacity of 348.7 m Ah·g^(-1)was achieved for Ni_(0.5)Cr_(7.5)O_(21),much higher than 271.4 m Ah·g^(-1)of the un-doped sample,with an increase of more than 28%.Electrochemical impedance spectroscopy results confirm that Ni doping reduces the growth of interface resistance and charge transfer resistance,which is conducive to the electrochemical kinetic behaviors during charge-discharge.

关键词： Cr_(8)O_(21) cathode material doping electrochemical performances lithium-ion batteries

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Enhancing proton exchange membrane water electrolysis by building electron/proton pathways

Advanced Powder Materials

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advanced Powder materials 2024年第4期3卷 103-112页

作者： Liyan Zhu Hao Zhang Aojie Zhang Tian Tian Yuhan Shen Mingjuan Wu Neng Li Haolin Tang State Key Laboratory of Advanced Technology for Materials Synthesis and Processing State Key Laboratory of Silicate Materials for ArchitecturesWuhan University of TechnologyWuhan 430070China National Energy Key Laboratory for New Hydrogen-ammonia Energy Technologies Foshan Xianhu LaboratoryFoshan 528200China Hubei Key Laboratory of Fuel Cell Wuhan 430070China

Proton exchange membrane water electrolysis(PEMWE)plays a critical role in practical hydrogen *** for the electrode activities,the widespread deployment of PEMWE is severely obstructed by the poor electron-proton permeability across the catalyst layer(CL)and the inefficient transport *** this work,the PEDOT:F(Poly(3,4-ethylenedioxythiophene):perfluorosulfonic acid)ionomers with mixed proton-electron conductor(MPEC)were fabricated,which allows for a homogeneous anodic CL structure and the construction of a highly efficient triple-phase *** PEDOT:F exhibits strong perfluorosulfonic acid(PFSA)side chain extensibility,enabling the formation of large hydrophilic ion clusters that form proton-electron transport channels within the CL networks,thus contributing to the surface reactant water *** PEMWE device employing membrane electrode assembly(MEA)prepared by PEDOT:F-2 demonstrates a competitive voltage of 1.713 V under a water-splitting current of 2 A cm^(-2)(1.746 V at 2A cm^(-2) for MEA prepared by Nafion D520),along with exceptional long-term ***,the MEA prepared by PEDOT:F-2 also exhibits lower ohmic resistance,which is reduced by 23.4%and 17.6%at 0.1 A cm^(-2) and 1.5 A cm^(-2),respectively,as compared to the MEA prepared by *** augmentation can be ascribed to the superior proton and electron conductivity inherent in PEDOT:F,coupled with its remarkable structural *** characteristic enables expeditious mass transfer during electrolytic reactions,thereby enhancing the performance of PEMWE devices.

关键词： Proton exchange membrane water electrolysis Oxygen evolution reaction Mixed proton-electron conductivity Triple-phase boundaries Membrane electrode assembly

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High thermoelectric performance of flexible Ag/Ag_(2)Se composite film on nylon for low-grade energy harvesting

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Journal of materials Science & technology 2024年第12期179卷 79-85页

作者： Ying Liu Jiajia Li Zixing Wang Ping Wei Wenyu Zhao Lidong Chen Kefeng Cai Key Laboratory of Advanced Civil Engineering Materials of Ministry of Education Shanghai Key Laboratory of Development and Application for Metal-Functional MaterialsSchool of Materials Science&EngineeringTongji UniversityShanghai 201804China State Key Laboratory of High Performance Ceramics and Superfine Microstructure Shanghai Institute of CeramicsChinese Academy of SciencesShanghai 200050China University of Chinese Academy of Sciences Beijing 100049China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China

In this work,Ag/Ag_(2)Se composite films with excellent thermoelectric(TE)properties and flexibility are prepared based on a simple one-pot *** adjusting the nominal ratios of Ag/Se,an optimal Ag/Ag_(2)Se composite film shows a large power factor of~2275 μW m^(-1) K^(-2) at 300 *** an outstand-ing TE performance of the composite film is due to the unique microstructure and the synergistic effect between the Ag and Ag_(2)***,the composite film also shows outstanding flexibility(~91.8%of the initial electrical conductivity is maintained,and the S is unchanged after 1500 bending cycles with a bending radius of 4 mm).Furthermore,a 4-leg flexible TE generator assembled with the optimal film produces a voltage of 14.06 mV and 4.96 μW at a temperature difference of 30.4 *** work provides a new inspiration for the preparation of flexible Ag_(2)Se-based films with excellent TE performance near room temperature.

关键词： Thermoelectric Ag/Ag_(2)Se Flexible Film Power generator

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Continuous Fe^(3+)releasing enabled complete reconstruction of Ni-based MOF for promoted water oxidation in industrial alkali

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Science China Chemistry 2024年第9期67卷 2949-2957页

作者： Zhaojian Wang Wei Zhang Wenzhong Huang Ruohan Yu Changliang Chen Liqiang Mai Liang Zhou State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Sanya Science and Education Innovation Park Wuhan University of TechnologySanya 572000China Hubei Longzhong Laboratory Wuhan University of Technology(Xiangyang Demonstration Zone)Xiangyang 441000China

Most oxygen evolution reaction(OER)electrocatalysts show poor stability under industrial alkaline conditions(20–30 wt.%KOH).Therefore,it is essential to develop stable,efficient,and low-cost OER catalysts for industrial water ***,we present a straightforward approach for the complete electrochemical reconstruction of Ni-BDC,a Ni-based metal-organic framework,for *** method involves the continuous release of Fe^(3+)from Fe foam counter electrode in a high-concentration(6.0 M,25 wt.%)KOH *** continuously Fe^(3+)releasing not only realizes in situ Fe^(3+)doping,but also introduces abundant defects in the obtained catalyst during cyclic voltammetry activation,thereby accelerating the electrochemical *** reconstructed OER catalyst(Fe-doped nickel hydroxide/oxyhydroxide nanosheets supported on Ni foam,Fe-NiO_(x)(OH)y/NF)manifests a low overpotential of 217 mV at 10 mA cm^(-2)and 263 m V at 100 m A cm^(-2)in 1.0 M ***,the Fe-NiO_(x)(OH)_(y)/NF also demonstrates high stability in 30 wt.%*** strategy of regulating the electrochemical reconstruction process sheds light on the construction of stable and efficient OER catalysts for industrial water electrolysis.

关键词： oxygen evolution reaction industrial alkaline conditions metal-organic framework complete reconstruction

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The Shock Response and Spall Mechanism of Mg-Al-Zn Alloy:Molecular Dynamics Study

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Acta Mechanica Solida Sinica 2022年第3期35卷 495-503页

作者： Xiaoyue Yang Shuang Xu Lisheng Liu Hubei Key Laboratory of Theory and Application of Advanced Materials Mechanics Wuhan University of TechnologyWuhan 430070China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China

Shock responses of Mg-Al-Zn alloy are investigated by the molecular dynamics(MD)*** wave propagation,plastic deformation behavior and failure mechanism along the[0001]and[1010]orientations are *** both orientations,simulation results show that the shock wave has an obvious double-wave structure(plastic-elastic)under a piston velocity of 1200 m/s.A higher Hugoniot elastic limit(HEL)is observed for[0001]-oriented *** the shock pressure is along the[1010]direction,the distance between plastic and elastic waves is closer,and higher dislocation density and more twins are ***,the spall strength for[1010]-oriented shock is predicted to be *** addition,the wave interactions,HEL and spall strength predicted for Mg-Al-Zn alloy are compared with the experimental results and MD simulation results of Mg single crystal in the *** is concluded that the shock performance of Mg-Al-Zn is better than that of Mg single crystal.

关键词： Mg-Al-Zn Shock compression Molecular dynamics Hugoniot elastic limit Spall strength

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Efficient overall photosynthesis of H_(2)O_(2) by the BTz@Mn_(0.2)Cd_(0.8)S S-scheme heterojunction

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Science China Chemistry 2024年第6期67卷 1953-1960页

作者： Zhongyue Chen Sijie Wan Bei Cheng Wang Wang Yao Xiang Jiaguo Yu Shaowen Cao State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan430070China Hubei Technology Innovation Center for Advanced Composites Wuhan University of TechnologyWuhan430070China Hospital of Wuhan University of Technology Wuhan University of TechnologyWuhan430070China Laboratory of Solar Fuel Faculty of Materials Science and ChemistryChina University of GeosciencesWuhan430074China

The photosynthesis of hydrogen peroxide(H_(2)O_(2))through the selective 2e^(-)oxygen reduction reaction(ORR)from O_(2)and H_(2)O stands out as an environmentally sustainable and cost-effective method for generating this essential ***,the widespread application of most photocatalysts is impeded by their reliance on sacrificial *** this context,we present a noteworthy advancement in the form of a step-scheme(S-scheme)heterojunction involving a donor-acceptor(D-A)-conjugated polymer and manganese cadmium sulfide(BTz@MCS).This innovative configuration enables efficient photocatalytic H_(2)O_(2)production within a non-sacrificial system,showcasing an impressive H_(2)O_(2)yield of 5,368μmol g^(-1)h^(-1)and an apparent quantum yield of 4.5%at 420 *** insights gained from in-situ irradiated X-ray photoelectron spectroscopy(ISIXPS),in-situ diffuse reflectance infrared Fourier transformations spectroscopy(DRIFTS),and density function calculations(DFT),it is revealed that the sp^(2)C between thiazole-thiazole rings at the BTz and the concentrated holes at the MCS function as spatially separated redox *** centers catalyze the selective 2e^(-)ORR and 4e^(-)water oxidation reaction(WOR)*** O_(2)generated from the WOR is subsequently utilized by the ORR cycle,enabling the overall photosynthesis of H_(2)O_(2)with accelerated total reaction ***,the high photocatalytic performance of the developed catalyst is attributed to well-designed S-scheme heterojunctions with tuned band *** spatially separated redox centers and effective transfer of photogenerated charge carriers facilitated by the internal electric field significantly enhance reaction *** study introduces a promising avenue for photocatalytic H_(2)O_(2)production without sacrificial agents,providing valuable insights into the underlying mechanisms in S-scheme heterojunctions.

关键词： hydrogen peroxide non-sacrificial redox centers S-scheme heterojunction

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Unraveling the Role of Nitrogen-Doped Carbon Nanowires Incorporated with MnO_(2)Nanosheets as High Performance Cathode for Zinc-Ion Batteries

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Energy & Environmental materials 2023年第3期6卷 205-213页

作者： Xiaohui Li Qiancheng Zhou Ze Yang Xing Zhou Dan Qiu Huajun Qiu Xintang Huang Ying Yu Institute of Nanoscience and Technology College of Physical Science and TechnologyCentral China Normal UniversityWuhan 430079China State Key Laboratory of Advanced Technology for Materials Synthesis and processing Wuhan University of Technology Wuhan 430070China

Manganese-based cathode materials are considered as a promising candidate for rechargeable aqueous zinc-ion batteries(ZIBs).Suffering from poor conductive and limited structure tolerance,various carbon matrix,especially N-doped carbon,were employed to incorporate with MnO_(2)for greatly promoted electrochemical ***,the related underlying mechanism is still unknown,which is unfavorable to guide the design of high performance ***,by incorporating layered MnO_(2)with N-doped carbon nanowires,a free-standing cathode with hierarchical core-shell structure(denoted as MnO_(2)@NC)is *** from the N-doped carbon and rational architecture,the MnO_(2)@NC electrode shows an enhanced specific capacity(325 mAh g^(−1)at 0.1 A g^(−1))and rate performance(90 mAh g^(−1)at 2 A g^(−1)),as well as improved cycling ***,the performance improvement mechanism of MnO_(2)incorporated by N-doped carbon is investigated by X-ray photoelectron spectroscopy(XPS),Raman spectrums and density functional theory(DFT)*** N atom elongates the Mn-O bond and reduces the valence of Mn^(4+)ion in MnO_(2)crystal by delocalizing its electron ***,the electrostatic repulsion will be weakened when Zn^(2+)/H^(+)insert into the host MnO_(2)lattices,which is profitable to more cation insertion and faster ion transfer kinetics for higher capacity and rate *** work elucidates a fundamental understanding of the functions of N-doped carbon in composite materials and shed light on a practical pathway to optimize other electrode materials.

关键词： core-shell nanostructure MnO_(2)nanosheets N-doped carbon Zn ion batteries

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Highly efficient and stable electrocatalyst for hydrogen evolution by molybdenum doped Ni-Co phosphide nanoneedles at high current density

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Nano Research 2024年第3期17卷 1066-1074页

作者： Chengyu Huang Zhonghong Xia Jing Wang Jing Zhang Chenfei Zhao Xingli Zou Shichun Mu Jiujun Zhang Xionggang Lu Hong Jin Fan Shengjuan Huo Yufeng Zhao College of Sciences&Institute for Sustainable Energy Shanghai UniversityShanghai 200444China State Key Laboratory of Metastable Materials Science and Technology Hebei Key Laboratory of Heavy Metal Deep-Remediation in Water and Resource ReuseYanshan UniversityQinhuangdao 066004China State Key Laboratory of Advanced Special Steel and Shanghai Key Laboratory of Advanced Ferrometallurgy School of Materials Science and EngineeringShanghai UniversityShanghai 200444China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China School of Physical and Mathematical Sciences Nanyang Technological UniversitySingapore639798

There is an increasingly urgent need to develop cost-effective electrocatalysts with high catalytic activity and stability as alternatives to the traditional Pt/C in catalysts in water *** this study,microspheres composed of Mo-doped NiCoP nanoneedles supported on nickel foam were prepared to address this *** results show that the nanoneedles provide sufficient active sites for efficient electron transfer;the small-sized effect and the micro-scale roughness enhance the entry of reactants and the release of hydrogen bubbles;the Mo doping effectively improves the electrocatalytic performance of NiCoP in alkaline *** catalyst exhibits low hydrogen evolution overpotentials of 38.5 and 217.5 mV at a current density of 10 mA·cm^(-2) and high current density of 500 mA·cm^(-2),respectively,and only 1.978 V is required to achieve a current density of 1000 mA·cm^(-2) for overall water *** functional theory(DFT)calculations show that the improved hydrogen evolution performance can be explained as a result of the Mo doping,which serves to reduce the interaction between NiCoP and intermediates,optimize the Gibbs free energy of hydrogen adsorption(△G_(*H)),and accelerate the desorption rate of **** study provides a promising solution to the ongoing challenge of designing efficient electrocatalysts for high-current-density hydrogen production.

关键词： transition metal phosphides Mo-doped NiCoP hydrogen evolution reaction gradient hydrothermal water splitting

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