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Size effect enabling additive-free MXene ink with ultrahigh conductivity for screen printing of wireless electronics

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Nano Research 2023年第8期16卷 11012-11017页

作者： Shuaishuai Chen Huaqiang Fu Yunfa Si Xueyu Liu Zhe Wang Yixue Duan Zixin Zhang Hao Feng Xin Zhao Daping He State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Hubei Engineering Research Center of RF-Microwave Technology and Application Wuhan University of TechnologyWuhan 430070China School of Science Wuhan University of TechnologyWuhan 430070China

Facile preparation of additive-free inks with both high viscosity and high conductivity is critical for scalable screen printing of wireless electronics,yet very *** materials exhibit excellent conductivity and hydrophilicity,showing great potential in the field of additive-free inks for screen ***,we demonstrate the synthesis of additive-free two-dimensional(2D)titanium carbide MXene inks,and realize screen-printed MXene wireless electronics for the first *** viscosity of MXene ink is solely regulated by tuning the size of MXene nanosheet without any additives,hence rendering the printed MXene film extremely high conductivity of 1.67×10^(5) S/m and fine printing resolution down to 0.05 mm on various flexible ***,radio frequency identification(RFID)tags fabricated using the additive-free MXene ink via screen printing exhibit stable antenna reading performance and superb *** article,thus offers a new route for the efficient,low-cost and pollution-free manufacture of printable electronics based on additive-free MXene inks.

关键词： size effect additive-free MXene ink screen printing wireless electronics radio frequency identification(RFID)

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Modification of sulfonated poly(arylene ether nitrile) proton exchange membranes by poly(ethylene-co-vinyl alcohol)

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RSC Advances 2023年第16期13卷 11062-11068页

作者： Liu, Hao Dong, Tiandu Zhou, Mingzheng Zhang, Zetian Li, Yunxi Lu, Chuanrui Liu, Yichen Zhao, Shengqiu Zheng, Shuhong Meng, Zihan Tang, Haolin State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China State Power Investment Corporation Hydrogen Energy Company Ltd. Co. Beijing China

The modification of the physicochemical properties of sulfonated poly(arylene ether nitrile) (SPAEN) proton exchange membranes was demonstrated by poly(ethylene-co-vinyl alcohol) (EVOH) doping (named SPAEN-x%). By controlling the temperature during membrane preparation, the side reactions of the sulfonic acid groups to form sulfonic acid esters were effectively prevented, greatly reducing the proton conductivity of the membranes. Due to the flexible chain of EVOH, SPAEN-8% showed a relatively high elongation of 30.2%, which enhanced the aromatic polymers' flexibility. The SPAEN-2% membrane exhibited proton conductivity of 166, 55, and 9.6 mS cm−1 at 95%, 70%, and 50% relative humidity, respectively, higher than those of the other SPAEN-x% membranes and even comparable to that of Nafion 212. The water uptake, morphological study, and through-plane proton conductivity of the membranes were studied and discussed. The results suggest that EVOH doping can be used as an effective strategy to improve SPAEN-based proton exchange membranes' performance. © 2023 The Royal Society of Chemistry.

关键词： Membranes

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

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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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Nonflammable electrolyte with weak-solvation structure for stable NCM811 cathode under high temperature

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Journal of Energy Chemistry 2025年第5期104卷 111-117页

作者： Dawei Xu Chao Yang Ailing Yang Xiaowei Liu Meilong Wang Jin Han Tiefeng Liu Ya You State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070HubeiChina International School of Materials Science and Engineering School of Materials Science and MicroelectronicsWuhan University of TechnologyWuhan 430070HubeiChina College of Chemical and Biological Engineering Zhejiang UniversityHangzhou 310058ZhejiangChina Quzhou Institute of Power Battery and Grid Energy Storage Quzhou 324000ZhejiangChina

High-nickel cathode LiNi_(0.8)Co_(0.1)Mn_(0.1)O_(2)(NCM811)could enable lithium-ion batteries(LIBs)with high energy ***,excessive decomposition of the electrolyte would happen in the high operating voltage *** addition,the utilization of flammable organic solvents would increase safety risks in the high temperature ***,an electrolyte consisting of flame-retardant solvents with lower highest occupied molecular orbital(HOMO)level and LiDFOB salt is proposed to address above two *** a result,a thin and robust cathode-electrolyte interface containing rich LiF and Li-B-O compounds is formed on the cathode to effectively suppress electrolyte decomposition in the high operating *** NCM811||Li cell paired with this designed electrolyte possesses a capacity retention of 72%after 300 cycles at 55℃.This work provides insights into developing electrolyte for stable high-nickel cathode operated in the high temperature.

关键词： Electrolyte engineering Weak solvation High temperature Safety High-nickel cathode

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Structural Evolution of Graphene Oxide and Its Thermal Stability During High Temperature Sintering

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Journal of Wuhan University of technology(materials Science) 2022年第3期37卷 342-349页

作者： HU Lanxin WANG Aiyang WANG Weimin School of Materials Science and Engineering Wuhan University of TechnologyWuhan 430070China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China

The thermal reduction of graphene oxide(GO)was performed by a tube furnace at different temperatures,and its structure evolution was investigated in *** results showed that the oxygen-containing functional groups on the carbon plane surface of GO gradually decomposed as the temperature increase,and the reduced graphene oxide(rGO)powder was obtained at 800℃.Then,rGO powder was sintered under 30 MPa at 1800℃using spark plasma sintering(SPS)and hot-pressing(HP)to evaluate its structural stability at high *** defect densities of rGO were reduced after high-temperature *** edge flatness and sp^(2) hybrid carbon plane structure were reconstructed *** results demonstrate that the lamellar structure of rGO maintains the structural integrity during high-temperature sintering without obvious deterioration,which provides experimental and theoretical supports for GO reinforced ceramics.

关键词： graphene oxide ceramics structure evolution thermal stability sintering

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Dynamic photoluminescence switching of carbon nitride thin films for anticounterfeiting and encryption

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Chinese Journal of Structural Chemistry 2024年第10期43卷 49-54页

作者： Hang Meng Bicheng Zhu Ruolun Sun Zixuan Liu Shaowen Cao Kan Zhang Jiaguo Yu Jingsan Xu School of Chemistry and Physics and Centre for Materials Science Queensland University of TechnologyBrisbaneQueensland4000Australia Laboratory of Solar Fuel Faculty of Materials Science and ChemistryChina University of GeosciencesWuhan430074China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan430070China Department of Materials Science and Key Laboratory of Automobile Materials MOEState Key Laboratory of Superhard MaterialsJilin UniversityChangchun130012China

Photoluminescence(PL)has been increasingly applied in anticounterfeiting and encryption as counterfeiting becomes more ***,common luminescent encryption techniques are based on static PL mea-surements and are easy to *** this work,we have developed a thermal vapor deposition(TVD)approach using melem as the unique starting material to synthesize highly homogeneous carbon nitride(CN)thin films featuring unique dynamic PL switching *** being irradiated by a white LED,the blue PL in-tensity of the CN film increases significantly and then fades in darkness,demonstrating excellent *** results prove that CN films contain cyano groups in the structure,and density functional theory(DFT)calculations indicate that the integration of cyano groups results in traps within the bandgap of CN,sug-gesting that the dynamic PL switching effect is essentially associated with the fullness of the trap *** have therefore developed an advanced luminescent device for the secure transmission of encrypted information through controlled *** can be easily read with a portable UV(365 nm)lamp and effectively erased using the white LED,thereby preventing information leakage and showing great potential for many applications.

关键词： Thermal vapor deposition Carbon nitride film Dynamic photoluminescence Encryption

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Bioprocess-inspired Actin Biomineralized Hematite Mesocrystals for Energy Storage

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Journal of Wuhan University of technology(materials Science) 2023年第6期38卷 1299-1303页

作者： XU Wei ZHAO Chao XIE Jingjing WANG Rongjie Tianjin Institute of Power Sources Tianjin 300384China CETC LAN TIAN Technology Co. Ltd.Tianjin 300384China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China

Biomineralization is a biological process of synthesizing inorganic minerals within *** has been found that intracellular proteins are involved in the room temperature synthesis process of anatase Ti O2in living ***,we used intracellular actin to synthesize hematite by *** hematite has a nano spindle structure with a particle size of approximately 150 *** microstructure indicates that the prepared hematite is a mesocrystals composed of ordered arrangement and assembly of primary *** addition,hematite mesocrystals exhibit good lithium storage performance as electrode materials for lithium *** discharge specific capacity of the battery remained at 560.7 m Ah·g^(-1)after 130 cycles at a current density of 200 m A·g^(-1).This work expands the synthesis methods of hematite by biomineralization,and provides a new strategy for preparing inorganic materials by intracellular proteins.

关键词： actin hematite biomineralization mesocrystals lithium battery

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Effect of Y:Zn ratio on microstructure and emission of Er^(3+)/Yb^(3+) codoped Y_(2)O_(3)-ZnO ceramic phosphors

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Journal of Rare Earths 2023年第12期41卷 1883-1894,I0003页

作者： Boxu Xu Chao Song Jie Song Rui Huang Shaomin Lin Zhenxu Lin Yi Zhang Dejian Hou Jun Song School of Materials Science and Engineering Hanshan Normal UniversityChaozhou521041China Key Laboratory of Optoelectronic Devices and Systemsof MinistryofEducation and Guangdong Province College of Optoelectronic EngineeringShenzhen UniversityShenzhen518060China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan430070China

In this study,Er^(3+)/Yb^(3+)codoped Y_(2)O_(3)-ZnO ceramic phosphors were prepared by sol-gel *** samples had two emission bands,namely,green(535 nm) and red(660 nm),which are attributed to Er^(3+):^(2)H_(11/2)(^(4)S_(3/2))→^(4)I_(15/2)and Er^(3+):^(4)F_(9/2)→^(4)I_(15/2)radiative transitions,*** samples exhibited green-and red-emission intensity enhancement by 1.728 and 2.286 times that of the pure Y2O3host,respectively and by 514.468 and 214.341 times that of the pure ZnO *** emission intensities are first enhanced by lattice *** the change of Y:Zn ratio,the high surface energy is converted into low crystal surface resulting in the change of asymmetry crystal field for *** the intensity of the asymmetric crystal field reaches maximum,both emissions are further *** the high surface energy transforms into crystal surface energy,the microstructure changes into a compact mesoporous ***,the chemical stability of the samples improves significantly,and the final emission band of the three samples with mesoporous structures is continuously red.

关键词： Mesoporous Y_(2)0_(3) Zno Luminescence Rare earths Ceramic phosphors

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ZnIn_(2)S_(4)/MOF S-scheme photocatalyst for H_(2)production and its femtosecond transient absorption mechanism

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Journal of materials Science & technology 2024年第30期197卷 183-193页

作者： Jiajie Cai Bowen Liu Shumin Zhang Linxi Wang Zhen Wu Jianjun Zhang Bei Cheng State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Hunan Key Laboratory of Applied Environmental Photocatalysis Changsha UniversityChangsha 410022China Laboratory of Solar Fuel Faculty of Materials Science and ChemistryChina University of Geosciences68 Jincheng StreetWuhan 430078China Department of Chemical Engineering Ordos Institute of TechnologyOrdos 017000China

Photocatalytic water splitting is a popular pathway for H_(2)evolution,but the slow water oxidation greatly hampers the overall *** harness photogenerated holes in an efficient and lucrative way,the wa-ter oxidation reaction is replaced by selective oxidation of organic compounds to achieve simultaneous production of H_(2)and value-added ***,an alternative tactic is reported where an organic compound(benzylamine,BA)not only serves as the precursor for N-benzylidene-benzylamine(NBBA)production but also provides hydrogen sources for H_(2)evolution,achieving the goal under anhydrous *** process is realized using an S-scheme photocatalyst composed of ZnIn_(2)S_(4)and the UiO-66-NH_(2)(U6N)metal-organic framework(MOF).The S-scheme carrier transfer mechanism was validated by in-situ irradiated X-ray photoelectron spectroscopy(ISI-XPS)and femtosecond transient absorption(fs-TA)*** increased carrier efficiency and reinforced redox power endowed by the S-scheme heterojunction,the composite performed better than ZnIn2 S4 and *** performance was further ameliorated by Pt-cocatalyst modification,achieving an H_(2)production rate of 5275μmol h^(-1)g^(-1)as well as BA conversion of 94.3%with 99.3%NBBA *** studies reveal that BA is ini-tially oxidized to carbon-centered radicals and further to imines along with the release of *** imine reacts with another BA molecule to form NBBA,while the protons are reduced to H_(2).This work provides new insights into concurrent photocatalytic H_(2)production and selective organic oxidation from organic amines using S-scheme photocatalysts.

关键词： Photocatalysis S-scheme heterojunction Hydrogen production Selective oxidation Benzylamine Femtosecond transient absorption

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Weakly solvating electrolyte enabling solvent-free co-intercalation for stable potassium-ion storage in graphite

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Nano Research 2025年第3期18卷 234-242页

作者： Chaojie Cheng Wencong Feng Feiyue Wang Jingke Ren Deyang Guan Wei Chen Jean-Jacques Gaumet Kai Fu Xiaobin Liao Wen Luo State Key Laboratory of Advanced Technology for Materials Synthesis and Processing School of Materials Science and EngineeringWuhan University of TechnologyWuhan 430070China School of Materials Science and Engineering Xinjiang UniversityUrumqi 830017China Laboratoire de Chimie et Physique:Approche Multi-échelles des Milieux Complexes(LCP-A2MC)Institut Jean BarriolUniversitéde LorraineMetz 57070France

Ether electrolytes for potassium-ion batteries exhibit a broader electrochemical window and greater applicability,yet most of them are high-concentration electrolytes with elevated *** this study,we propose the use of a weakly solvating cyclic ether electrolyte with tetrahydropyran(THP)as the *** approach induces the formation of a thin and dense inorganic-rich solid electrolyte interphase(SEI)film,which is accompanied by a decrease in the activation energy of electrode interfacial reactions due to the weak ligand binding of THP with K^(+).Density functional theory(DFT)simulations also corroborate the hypothesis that K^(+)has a lower binding energy with *** potassium storage process,the phenomenon of solvent co-intercalation of graphite does not occur,which greatly reduces the destruction of the graphite structure and enables a superior electrochemical performance and enhanced cycling stability at a lower concentration(2 M).At a current density of 0.2 C(55.8 mA·g^(-1)),the battery can be stably cycled for 800 cycles(approximately 8 months)with a specific capacity of 171.8 mAh·g^(-1).This study provides a new ether-based electrolyte for potassium ion batteries and effectively reduces the electrolyte cost,which is expected to inspire further development of energy storage batteries.

关键词： weakly solvating electrolyte co-intercalation graphite potassium ion batteries

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