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SSRN 2023年

作者： Chang, Baisong Dong, Kangfeng Wu, Shaolong Sun, Taolei State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China School of Chemistry Chemical Engineering and Life Science Wuhan University of Technology Wuhan430070 China

The presence of different types of organic dyes in water stream will clearly give rise to unexceptional side effects on living organisms. Emerging physical or chemical methods have been developed for the treatment of dye-involving water, but the exploration for adequate design strategy and technique available is still ongoing. Here, the zero-valent iron (ZVI) was prepared by a liquid phase sodium borohydride reduction approach and then integrated with dendritic mesoporous silica nanoparticle (DMSN) to construct the Janus magnetic adsorbent (denoted as ZVI-DMSN), which could be employed to purify dye wastewater. The structure, magnetic properties and dye adsorption results of ZVI-DMSN were systematically investigated. The ZVI component can enable efficient solid-liquid separation through magnetic separation route, and, more importantly, provided additional binding sites for adsorption process to increase the adsorption capacity. The thermodynamic analysis of adsorption indicated that the adsorption of typical organic dyes was an irreversible, spontaneous and endothermic process. Moreover, ZVI-DMSN adsorbent was recyclable, showing a regeneration efficiency of more than 80% after 5 cycles. We believe that ZVI-DMSN, as an inexpensive adsorbent material with excellent adsorption properties, e.g., short time, high efficiency and large capacity, will host vast potential for removal of dyes in water bodies. © 2023, The Authors. All rights reserved.

关键词： Wastewater treatment

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Binder-free electrodes for advanced potassium-ion batteries:A review

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Chinese Chemical Letters 2021年第4期32卷 1299-1308页

作者： Wencong Liu Wenyi Liu Yuqi Jiang Qiuyue Gui Deliang Ba Yuanyuan Li Jinping Liu School of Chemistry Chemical Engineering and Life ScienceState Key Laboratory of Advanced Technology for Materials Synthesis and ProcessingWuhan University of TechnologyWuhan 430070China School of Optical and Electronic Information Huazhong University of Science and TechnologyWuhan 430074China Key Laboratory for Photonic and Electronic Bandgap Materials Ministry of EducationSchool of Physics and Electronic EngineeringHarbin Normal University.Harbin 150025China

Potassium-ion batteries(PIBs)have attracted enormous attention due to the abundance of potassium resources,low cost,fast ionic conductivity of electrolyte and relatively high operating *** great effo rts and progress,researches on PIBs are still at the initial stage,especially in the emerging field of flexible and wearable *** inevitable challenges for PIBs include low reversible capacity,unsatisfactory cycling stability and insufficient energy density,the solution to which mostly relies on designing adva nced ***-free electrodes have emerged as promising electrode architecture for *** electrodes avoid the use of insulating binders,which can be designed with various synergistic functional materials to address the aforementioned PIB issues and be endowed with flexibility/*** this review,we mainly summarize the recent progress on binde r-free electrodes for PIBs,with the focus on the methodologies,detailed strategies and functional materials for electrode *** strategy for binder-free electrodes is to assemble free-standing architecture with the help of carbon nanotubes(CNTs),graphitic fibers,and other carbon or mechanically robust materials,either alone or in *** other effective strategy is current collector substrate-assisted direct growth,including the use of carbon cloth,*** and other conductive ***,challenges and research opportunities are put forward at the end as the guidance for future development of binder-free PIB devices.

关键词： Binder-free Free-standing electrode Substrate-assisted directly grown electrode Potassium-ion battery Flexible device

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Rational synthesis of Cylindrical Silver Single-crystalline Nanowires via Poly(vinyl pyrrolidone) Reduction of AgCl

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Journal of Wuhan University of technology(materials Science) 2020年第3期35卷 473-481页

作者： DUAN Junyuan YANG Rui HAN Meng LIU Bingxin WANG Yilong GUAN Jianguo State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China School of Mechanical Engineering Qinghai UniversityXining 810016China

We presented a simple yet convenient hydrothermal approach for the large-scale synthesis of uniform cylindrical silver (Ag) single-crystalline nanowires with diameters of about 25 nm and lengths of 1-4 μm. Poly(vinyl pyrrolidone) (PVP) was used as a reducing agent, and AgCl was used as a precursor to deliberately control [Ag^+] at a low degree in the overall reaction process through its dynamic equilibrium by directly reducing AgCl with PVP at a quasi-equilibrium growth condition. The as-obtained products were characterized by powder X-ray diffraction (XRD) patterns, field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), infrared spectra (IR) and Raman spectra. Factors such as [PVP], reaction temperature, time, and species of reducing agents and precursors were investigated to have strong influences on the morphologies and structures of the resultant Ag nanostructures. The wire diameter can conveniently be adjusted between 25 and 50 nm by simply adjusting [PVP], reaction temperature and reducing agent species. The as-synthesized silver nanowires can be self-assembled into perfect order arrays after being dried on tin foil due to the PVP coating on the surface, the circular cross-section and the uniform diameter of the Ag nanowires. These special silver nanowires with a core-shell structure as well as their spontaneous self-assembly of order arrays are expected to provide potential applications in flexible conductors, dielectric materials, electromagnetic shielding materials and nano-devices.

关键词： silver nanowires poly(vinyl pyrrolidone) hydrothermal approach self-assembly

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Dual synergetic catalytic effects boost hydrogen electric oxidation performance of Pd/W_(18)O_(49)

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Nano Research 2021年第7期14卷 2441-2450页

作者： Lingxin Peng Han Tian Xiangzhi Cui Liang Su Ge Meng Zhonghua Ma Shaowen Cao Jianlin Shi State Key Lab of High Performance Ceramics and Superfine Microstructure Shanghai Institute of CeramicsChinese Academy of SciencesShanghai 200050China Center of Materials Science and Optoelectronics Engineering University of Chinese Academy of SciencesBeijing 100049China School of Chemistry and Materials Science Hangzhou Institute for Advanced StudyUniversity of Chinese Academy of SciencesHangzhou 310024China School of Chemistry and Chemical Engineering Huazhong University of Science and Technology(HUST)Wuhan 430074China State Key Laboratory for Modification of Chemical Fibers and Polymer Materials&College of Materials Science and Engineering Donghua UniversityShanghai 201620China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China

Developing anode catalysts of substantially enhanced activity for hydrogen oxidation reaction(HOR)and anti-CO poisoning performance is of great importance for the application of proton exchange membrane fuel cells(PEMFCs).Herein,we report Pd cluster in situ decorated urchin-like W_(18)O_(49)(WO_(2.72))electrocatalysts by a photo-reduction method for high performance *** synthesized Pd-WO_(2.72)-L composite of low loading amount of 0.44 wt.%Pd by Xenon light reduction exhibits markedly high HOR catalytic activity and stability in 0.5 M H_(2)SO_(4),and the specific HOR current density and mass activity of Pd-WO_(2.72)-L are~1.5 and~80 times those of 20 wt.%Pt/C catalyst,***,excellent anti-CO poisoning ability has also been *** excellent HOR activity and anti-CO poisoning performance of Pd-WO_(2.72)-L have been discussed mainly in terms of the dual synergetic catalytic effects between Pd and WO_(2.72):Pd activation to Pd^(δ+)by the electron transfer from Pd to W promotes the hydrogen adsorption and activation to H*species,which results in largely elevated HOR activity;Pd degradation due to the CO poisoning is effectively prevented by WO_(2.72),which is responsible for the excellent CO-tolerance performance.

关键词： hydrogen oxygen reaction tungsten oxide photo-reduction method synergistic effect CO tolerance catalyst

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A new catalyst for urea oxidation: NiCo2S4 nanowires modified 3D carbon sponge

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Journal of Energy Chemistry 2020年第11期29卷 195-205页

作者： Biaopeng Li Congying Song Jianjun Rong Jing Zhao Hong-En Wang Ping Yang Ke Ye Kui Cheng Kai Zhu Jun Yan Dianxue Cao Guiling Wang Key Laboratory of Superlight Materials and Surface Technology of Ministry of Education College of Materials Science and Chemical EngineeringHarbin Engineering UniversityHarbin 150001HeilongjiangChina State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070HubeiChina

Urea oxidation is a significant reaction for utilizing urea-rich wastewater or human urine as sustainable power sources which can ease the water eutrophication while generate electricity. A direct urea-hydrogen peroxide fuel cell is a new kind of fuel cell employing urea as fuel and hydrogen peroxide as oxidant which possesses a larger cell voltage. Herein, this work tries to promote the kinetics process of urea oxidation by preparing low-cost and high-efficient NiCo2S4 nanowires modified carbon sponge electrode. The carbon sponge used in this work with a similar three-dimensional multi-channel structure to Ni foam, is prepared by carbonizing recycled polyurethane sponge which is also a process of recycling waste. The performance of the prepared catalyst in an alkaline solution is investigated in a three-electrode *** the introduction of Co element to the catalyst, a reduced initial urea oxidation potential and a high performance are obtained. Furthermore, a direct urea-hydrogen peroxide fuel cell is assembled using the NiCo2S4 nanowires modified carbon sponge anode. Results indicate that the prepared catalyst provides a chance to solve the current problems that hinder the development of urea electrooxidation(high initial urea oxidation potential, low performance, and high electrode costs).

关键词： Carbon sponge Direct urea fuel cell Electrocatalyst NiCo2S4 nanowires Urea oxidation

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In-depth understanding of ionic liquid assisted perovskite film formation mechanism for two-step perovskite photovoltaics

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Journal of Energy Chemistry 2022年第10期31卷 599-606,I0015页

作者： Fei Wang Patrick Wai-Keung Fong Zhiwei Ren Hai-Lun Xia Kang Zhou Kai Wang Jiajie Zhu Xiaoxi Huang Xiao-Yuan Liu Hao Wang Yumeng Shi Haoran Lin Quanyao Zhu Gang Li Hanlin Hu Hoffman Institute of Advanced Materials Shenzhen PolytechnicShenzhen 518055GuangdongChina Department of Electronic and Information Engineering Research Institute for Smart Energy(RISE)The Hong Kong Polytechnic UniversityHong Kong 999077China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing School of Materials Science and EngineeringWuhan University of TechnologyWuhan 43007HubeiChina International Collaborative Laboratory of 2D Materials for Optoelectronics Science and Technology of Ministry of Education Institute of Microscale OptoelectronicsShenzhen UniversityShenzhen 518060GuangdongChina The Hong Kong Polytechnic University Shenzhen Research Institute Shenzhen 518057GuangdongChina Institute of Flexible Electronics Northwestern Polytechnical UniversityXi’an 710072ShannxiChina School of Physics Science and Engineering Tongji UniversityShanghai 200092China

Ionic liquids(ILs)have been widely applied in the one-step fabrication of perovskite with noticeable enhancement in the device ***,in-depth mechanism of ionic-liquid-assisted perovskite film formation is not well understood for also important two-step perovskite fabrication method,with better control of crystallization *** this work,we introduced ionic liquid methylammonium formate(MAFa)into organic salt to produce perovskite film via a two-step *** investigations on the influence of MAFa on the perovskite thin film formation mechanism were *** liquid is shown to assist lowering the perovskite formation enthalpy upon the density functional theory(DFT)calculation,leading to an accelerated crystallization process evidenced by in-situ UV-Vis absorption measurement.A gradient up-down distribution of ionic liquid has been confirmed by timeof-flight ***,besides the surface passivation,we found the HCOO-can diffuse into the perovskite crystals to fill up the halide vacancies,resulting in significant reduction of trap *** perovskite films with significantly larger grains and less defect density were prepared with the help of MAFa IL,and the corresponding device efficiency over 23%was obtained by two-step process with remarkably improved *** research work provides an efficient strategy to tune the morphology and opto-electronic properties of perovskite materials via ionic-liquid-assisted two-step fabrication method,which is beneficial for upscaling and application of perovskite photovoltaics.

关键词： Halide vacancies Perovskite solar cells Two-step method Ionic liquid

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Electrolyte Concentration Regulation Boosting Zinc Storage Stability of High-Capacity K0.486V2O5 Cathode for Bendable Quasi-Solid-state Zinc Ion Batteries

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Nano-Micro Letters 2021年第2期13卷 232-245页

作者： Linpo Li Shuailei Liu Wencong Liu Deliang Ba Wenyi Liu Qiuyue Gui Yao Chen Zuoqi Hu Yuanyuan Li Jinping Liu School of Optical and Electronic Information Huazhong University of Science and TechnologyWuhan 430074People’s Republic of China School of Chemistry Chemical Engineering and Life Scienceand State Key Laboratory of Advanced Technology for Materials Synthesis and ProcessingWuhan University of TechnologyWuhan 430070People’s Republic of China Key Laboratory for Photonic and Electronic Bandgap Materials Ministry of EducationSchool of Physics and Electronic EngineeringHarbin Normal UniversityHarbin 150025People’s Republic of China

Vanadium-based cathodes have attracted great interest in aqueous zinc ion batteries(AZIBs)due to their large capacities,good rate performance and facile synthesis in large ***,their practical application is greatly hampered by vanadium dissolution issue in conventional dilute ***,taking a new potassium vanadate K0.486V2O5(KVO)cathode with large interlayer spacing(~0.95 nm)and high capacity as an example,we propose that the cycle life of vanadates can be greatly upgraded in AZIBs by regulating the concentration of ZnCl2 electrolyte,but with no need to approach“water-in-salt”*** the optimized moderate concentration of 15 m ZnCl2 electrolyte,the KVO exhibits the best cycling stability with ~95.02% capacity retention after 1400 *** further design a novel sodium carboxymethyl cellulose(CMC)-moderate concentration ZnCl2 gel electrolyte with high ionic conductivity of 10.08 mS cm^-1 for the first time and assemble a quasi-solid-state *** device is bendable with remarkable energy density(268.2 Wh kg^−1),excellent stability(97.35% after 2800 cycles),low self-discharge rate,and good environmental(temperature,pressure)suitability,and is capable of powering small *** device also exhibits good electrochemical performance with high KVO mass loading(5 and 10 mg cm^-2).Our work sheds light on the feasibility of using moderately concentrated electrolyte to address the stability issue of aqueous soluble electrode materials.

关键词： Electrolyte concentration regulation Quasi-solid-state Zn ion battery K0.486V2O5 Large interlayer spacing Cycling stability

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Microstructure,Mechanical,and Thermal Properties of B4C-TiB2-SiC Composites Prepared by Reactive Hot-pressing

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Journal of Wuhan University of technology(materials Science) 2020年第6期35卷 1031-1037页

作者： CAO Yaoqin HE Qianglong WANG Weimin China Helicopter Research and Development Institute Tianjin 300450China The State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China

B4C-TiB2-SiC composites with excellent properties were prepared by reactive hot-pressing using B4C,TiC,and Si powders as the raw *** phase transition process was investigated by heating the powder mixture to different temperatures and combined with XRD ***2 and SiC phases were synthesized through an in situ reaction,and the mechanical and thermal properties were improved *** and mechanical properties were also studied,and the 60wt% B4C-21.6wt% TiB2-18.4wt% SiC composite showed a relative density of 99.1%,Vickers hardness of 34.6 GPa,flexural strength of 582 MPa,and fracture toughness of 5.08 MPa·m1/*** addition,the values of thermal conductivity and thermal expansion coefficient were investigated,respectively.

关键词： B4C-TiB2-SiC reactive hot pressing microstructures mechanical properties thermal properties

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Highly Enhanced Electro-Catalytic Behavior of an Amide Functionalized Cu(Ii) Coordination Polymer on Oer at Large Current Densities

SSRN

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SSRN 2024年

作者： Afaq, Sheereen Ashiq, Faheem Shoukat, Wseem Malik, Wasif Mahmood Ahmed Ismail, Muhammad Ghafoor, Abdul Ashraf, Zohaib Sajjad, Muhammad Verpoort, Francis Chughtai, Adeel Hussain Institute of Chemical Sciences Bahauddin Zakariya University Multan60800 Pakistan Pakistan Moscow117198 Russia State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Center for Chemical and Material Engineering Wuhan University of Technology Wuhan430070 China

Extensive utilization of fossil fuels has led to their swift exhaustion, causing an escalating energy dilemma and significant environmental apprehensions. This situation has spurred advancement of sustainable energy conversion systems. Electrochemical water splitting is viewed as a capable method for generating hydrogen and oxygen intended for diverse electrochemical energy apparatus. A proficient, multifunctional electro-catalyst capable of facilitating both OERs) and HERs is of paramount importance. In this work, we report Cu-MOF electro-catalyst synthesized via the solvothermal route engaging OER activity using nickel foam (NF) in a 1 M KOH solution. Several analytical techniques were used to investigate the electro-catalysts BET, PXRD, FTIR and oxidation states. The water-splitting evaluation of the LOCOM-1 demonstrated exceptional oxygen activity concerning OER (oxygen evolution reaction), showcasing to extent a current density of 10 mAcm-2 a reduced of 286 mV over potential. Additionally, it exhibited a diminished onset potential of 1.37V attributable towards a decreased Tafel slope of 44.50 mVdec-1, and a proton couple electron transfer (PCET) channel that is stable over an extended period of time (1000 cycles of cyclic voltammetry and 40 hours of chronoamperometry). Therefore, this current endeavour might offer a new prospect or pathway for exploring the OER (Oxygen Evolution Reaction). © 2024, The Authors. All rights reserved.

关键词： Potassium hydroxide

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Ceramizable Cf/BPR composites with enhanced oxidation resistance up to 1670 °C

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Ceramics International 2025年

作者： Li, Junguo Zhao, Chenhan Jiang, Feng Zhang, Shiquan Yang, Suohui Xiang, Qianqian Li, Meijuan zhang, Jian Shen, Qiang School of Material Science and Engineering Wuhan University of Technology Wuhan430070 China School of Chemistry Chemical Engineering and Life Science Wuhan University of Technology Wuhan430070 China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China

Ceramizable carbon fiber/boron-modified phenolic resin (Cf/BPR) composites are cost-effective and suitable for fabricating large-scale components, making them vital for thermal protection systems in aerospace vehicles. However, their thermal resistance requires further improvement. This study investigates the modification of Cf/BPR composites using ZrSi2, Al, and mica to enhance their thermal resistance. High-temperature static oxidation and oxyacetylene ablation tests are conducted to evaluate their high-temperature performance. The role of each filler on oxidation resistance is discussed. The results reveal that when ZrSi2 is added at 33.75 phr, Al at 3.75 phr, and mica at 5 phr, the prepared composite exhibits a flexural strength of 56 MPa after 20 min of static oxidation at 1600 °C, with excellent protection of the carbon fibers. After oxidation at 1670 °C, the flexural strength remains at 45 MPa, despite some degree of carbon fiber ablation. © 2025 Elsevier Ltd and Techna Group S.r.l.

关键词： Carbon fibers

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