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In Situ Reaction Strengthening and Toughening of B_(4)C/TiSi_(2)Ceramics

Journal of Wuhan University of technology(materials Science) 2023年第1期38卷 12-19页

作者：夏涛涂晓诗张帆 ZHANG Jinyong REN Lin Hubei Longzhong Laboratory Wuhan University of TechnologyXiangyang Demonstration ZoneXiangyang 441000China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China School of Science Wuhan University of TechnologyWuhan 430070China

B_(4)C-SiC-TiB_(2)ceramics were prepared by in situ reactive hot-pressing sintering with TiSi_(2)as an *** reaction pathways of TiSi_(2)and B_(4)C were *** sintering was found to be a multistep *** reaction started at approximately 1000℃,and TiB_(2)was formed *** of Si and C started to react at 1300℃,and the unreacted Si melted at 1400℃to form a liquid ***_(2)predominantly affected the intermediate sintering process of B_(4)C and increased the sintering *** to the unique reaction process of TiSi_(2)and B_(4)C,a large number of aggregates composed of SiC and TiB_(2)were *** results showed that composite ceramics with the optimal flexural strength of 807 MPa,fracture toughness of 3.2 MPa·m1/2,and hardness of 32 GPa,were obtained when the TiSi_(2)content was 10 wt%.

关键词： in situ reaction hot pressing sintering TiSi_(2) B_(4)C composite ceramics reaction mechanism

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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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Ag掺杂n型Bi_(2)Te_(2.7)Se_(0.3)的层间相互作用增强和室温热电性能改善

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Science China materials 2023年第9期66卷 3651-3658页

作者：李龙魏平杨毛俊朱婉婷聂晓蕾赵文俞张清杰 State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China

采用Cu或Ag掺杂是提高n型Bi2Te3基合金热电性能的有效途径但Cu或Ag的掺杂行为仍不明确,其背后的作用机理还需要进一步证实本文对Ag掺杂n型Bi_(2)Te_(2.7)Se_(0.3)多晶热电材料的结构和输运性质进行了研究.拉曼和X射线光电子能谱分析表明... 详细信息

采用Cu或Ag掺杂是提高n型Bi2Te3基合金热电性能的有效途径但Cu或Ag的掺杂行为仍不明确,其背后的作用机理还需要进一步证实本文对Ag掺杂n型Bi_(2)Te_(2.7)Se_(0.3)多晶热电材料的结构和输运性质进行了研究.拉曼和X射线光电子能谱分析表明,Ag离子位于间隙位置,并向邻近的Te(Se)转移电子.Ag与Te(Se)成键导致层间相互作用增强,载流子迁移率升高.由于Ag–Te(Se)成键,Bi_(2)Te_(2.7)Se_(0.3)多晶的本征Te(Se)空位形成得到缓解,进而逐渐将载流子浓度调节到较低水平,因此Bi_(2)Te_(2.7)Se_(0.3)的室温热电性能得到显著改善.与单一Bi_(2)Te_(2.7)Se_(0.3)相比,最优Ag掺杂Bi_(2)Te_(2.7)Se_(0.3)材料的室温热电优值ZT和制冷性能分别提高近60%和75%.

关键词：热电性能制冷性能 Ag掺杂 X射线光电子能谱分析载流子迁移率热电材料热电优值载流子浓度

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Epitaxially Grown Ru Clusters-Nickel Nitride Heterostructure Advances Water Electrolysis Kinetics in Alkaline and Seawater Media

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Energy & Environmental materials 2023年第2期6卷 81-89页

作者： Jiawei Zhu Ruihu Lu Wenjie Shi Lei Gong Ding Chen Pengyan Wang Lei Chen Jinsong Wu Shichun Mu Yan Zhao State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Foshan Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong Laboratory Xianhu Hydrogen ValleyFoshan 528200China State Key Laboratory of Silicate Materials for Architectures International School of Materials Science and EngineeringWuhan University of TechnologyWuhan 430070China NRC(Nanostructure Research Centre) Wuhan University of TechnologyWuhan 430070China

The epitaxial heterostructure can be rationally designed based on the in situ growth of two compatible phases with lattice similarity,in which the modulated electronic states and tuned adsorption behaviors are conducive to the enhancement of electrocatalytic ***,theoretical simulations first disclose the charge transfer trend and reinforced inherent electron conduction around the epitaxial heterointerface between Ru clusters and Ni_(3)N substrate(cRu-Ni_(3)N),thus leading to the optimized adsorption behaviors and reduced activation energy ***,the defectrich nanosheets with the epitaxially grown cRu-Ni_(3)N heterointerface are successfully ***,by virtue of the superiority of intrinsic activity and reaction kinetics,such unique epitaxial heterostructure exhibits remarkable bifunctional catalytic activity toward electrocatalytic OER(226 mV@20 mA cm^(−2))and HER(32 mV@10 mA cm^(−2))in alkaline ***,it also shows great application prospect in alkaline freshwater and seawater splitting,as well as solar-to-hydrogen integrated *** work could provide beneficial enlightenment for the establishment of advanced electrocatalysts with epitaxial heterointerfaces.

关键词： alkaline water electrolysis bifunctional electrocatalyst epitaxial heterostructure seawater electrolysis solar-to-hydrogen integrated system

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Single-atom Cu anchored on N-doped graphene/carbon nitride heterojunction for enhanced photocatalytic H_(2)O_(2) production

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Journal of materials Science & technology 2023年第30期161卷 192-200页

作者： Han Li Bicheng Zhu Bei Cheng Guoqiang Luo Jingsan Xu Shaowen Cao State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Laboratory of Solar Fuel Faculty of Materials Science and ChemistryChina University of GeosciencesWuhan 430078China School of Chemistry and Physics Queensland University of TechnologyBrisbaneQLD 4000Australia

Photocatalytic production of H_(2)O_(2) by polymeric carbon nitride has been regarded as a promising ap-proach for the conversion of solar energy into valuable ***,the efficiency of pristine car-bon nitride is limited by the rapid charge recombination and the lack of suitable active ***,we introduce single-atom Cu anchored on N-doped graphene(Cu-NG)as a cocatalyst coupled with carbon nitride via covalent bonding to enhance photocatalytic H_(2)O_(2) *** Cu-NG/carbon nitride could broaden the light absorption from UV to near-infrared region,contributing to the photocatalytic ***,NG containing electron-rich N atoms could serve as anchoring sites for stabilizing single-atom ***,the single-atom Cu acts not only as an electron sink to steer the interfacial charge sep-aration but also as an active site for molecular oxygen adsorption and *** the synergistic effect of the enhanced interfacial charge separation and suitable active sites,Cu-NG/carbon nitride ex-hibits improved photocatalytic performance with an H_(2)O_(2) generation rate of 2856μmol g^(−1)h^(−1),which is 2.6 times that of pristine carbon *** work provides a protocol for high-performance photocat-alytic H_(2)O_(2) production using a single-atom cocatalyst.

关键词： Single-atom catalysis Interfacial charge separation Photocatalytic H_(2)O_(2)production

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Nanopore-rich NiFe LDH targets the formation of the high-valent nickel for enhanced oxygen evolution reaction

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Nano Research 2023年第2期16卷 2286-2293页

作者： Qunlei Wen Shuzhe Wang Ruiwen Wang Danji Huang Jiakun Fang Youwen Liu Tianyou Zhai State Key Laboratory of Materials Processing and Die&Mould Technology School of Materials Science and EngineeringHuazhong University of Science and TechnologyWuhan 430074China State Key Lab of Advanced Electromagnetic Engineering and Technology School of Electrical and Electronic EngineeringHuazhong University of Science and TechnologyWuhan 430074China

Nickel-iron layered double hydroxides(NiFe LDHs)represent a promising candidate for oxygen evolution reaction(OER),however,are still confronted with insufficient activity,due to the slow kinetics of electrooxidation of Ni^(2+)cations for the high-valent active ***,nanopore-rich NiFe LDH(PR-NiFe LDH)nanosheets were proposed for enhancing the OER activity together with *** the designed catalyst,the confined nanopores create abundant unsaturated Ni sites at edges,and decrease the migration distance of protons down to the scale of their mean free path,thus promoting the formation of high-valent Ni^(3+)/^(4+)active *** unique configuration further improves the OER stability by releasing the lattice stress and accelerating the neutralization of the local acidity during the phase ***,the optimized PR-NiFe LDH catalysts exhibit an ultralow overpotential of 278 mV at 10 mA∙cm^(−2)and a small Tafel slope of 75 mV∙dec^(−1),which are competitive among the advanced LDHs based ***,the RP-NiFe LDH catalyst was implemented in anion exchange membrane(AEM)water electrolyzer devices and operated steadily at a high catalytic current of 2 A over 80 *** results demonstrated that PR-NiFe LDH could be a viable candidate for the practical *** concept also provides valuable insights into the design of other catalysts for OER and beyond.

关键词： nickel-iron layered double hydroxides(NiFe LDHs) water oxidation nanopores high-valent sites

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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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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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