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SSRN 2024年

作者： Zhou, Meng-Jun Peng, Kun Tan, Yueze Yang, Tiannan Chen, Long-Qing Nan, Ce-Wen State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Center of Smart Materials and Devices School of Materials Science and Engineering Wuhan University of Technology Wuhan430070 China Department of Materials Science and Engineering Materials Research Institute The Pennsylvania State University University ParkPA16802 United States School of Mechanical Engineering Shanghai Jiao Tong University Shanghai200240 China School of Materials Science and Engineering State Key Lab of New Ceramics and Fine Processing Tsinghua University Beijing100084 China

Ferroelectric oxides with excellent flexibility are of significant practical and theoretical interests in recent studies. With most up-to-date research efforts, the effect of large bending on properties of nano-scale ferroelectric materials is still to be investigated. In this work, we elucidate the effect of bending angle on ferroelectric domain structures and material properties of bending PbTiO3 nanowires using phase-field simulations and thermodynamic modeling. We find non-monotonic dependencies of the coercive fields, dielectric responses and piezoelectric properties on the bending angle. A maximum enhancement of 462% and 226% in the dielectric constant and piezoelectric coefficient, respectively, is achieved at an 18° bending angle for the PbTiO3 nanowire with a radius of R = 10 nm and length L=100 nm, which is attributed to the formation of strong-response zones within the nanowire as illustrated by both the phase-field and thermodynamic analysis. The current work provides useful theoretical insights for the experimental explorations into ferroelectric functionalities of nanomaterials and potential applications of high-performance flexible ferroelectric-based nanodevices. © 2024, The Authors. All rights reserved.

关键词： Piezoelectricity

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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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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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Tris-based protic ionic liquids with multiple adsorption effects enabling excellent anti-wear and anti-corrosion performances

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Journal of Molecular Liquids 2025年 425卷

作者： Ge, Shanqin Chen, Long Li, Wei Cai, Qingzhao Gong, Genxiang Wu, Junhao Yu, Jinhong Nishimura, Kazuhito Jiang, Nan Cai, Tao School of Materials Science and Chemical Engineering Ningbo University Zhejiang Ningbo315211 China State Key Laboratory of Advanced Marine Materials Ningbo Institute of Materials Technology and Engineering Chinese Academy of Sciences Ningbo315201 China Advanced Nano-processing Engineering Lab Mechanical Engineering Kogakuin University Tokyo192-0015 Japan

Molecular additives have garnered widespread attention in the fields of lubrication and corrosion protection due to their designable interfacial film-forming efficiency. Herein, three protic ionic liquids (PILs) with the same cation but different anions have been designed and synthesized. Their physicochemical properties, tribological properties and anti-corrosion properties were systematically investigated. Results demonstrated that under dynamic steel-on-steel friction conditions, the PILs can maximally reduce the running-in period, friction coefficient, and wear rate by 90 %, 40 %, and 97 %, respectively, compared to the commercial ionic liquid, BMIMPF6. Under static copper corrosion conditions, the PILs efficiently adsorb onto the copper surface and formed a dense oxide layer on its surface, thus achieving excellent corrosion protection for the copper substrates. Molecular dynamics (MD) simulation results indicate that the exceptional lubricity of PILs is due to its ability to rapidly adsorb onto the metal surface through multiple interaction sites on both its anionic and cationic components, thereby reducing the running-in period and swiftly establishing a lubricating film. This study provides insights into the development of molecular additives featuring multiple adsorption sites, with potential applications in the fields of tribology and corrosion engineering. © 2025

关键词： Tribology

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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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Single-atomic Mn sites coupled with Fe_(3)C nanoparticles encapsulated in carbon matrixes derived from bimetallic Mn/Fe polyphthalocyanine conjugated polymer networks for accelerating electrocatalytic oxygen reduction

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Nano Research 2022年第9期15卷 7976-7985页

作者： Yuan Pan Min Li Wanliang Mi Minmin Wang Junxi Li Yilin Zhao Xuelu Ma Bin Wang Wei Zhu Zhiming Cui Hailiang Yin Yunqi Liu State Key Laboratory of Heavy Oil Processing China University of Petroleum(East China)Qingdao 266580China Key Laboratory of Advanced Energy Materials Chemistry(Ministry of Education) College of ChemistryNankai UniversityTianjin 300071China Research Institute of Petroleum Processing SinopecBeijing 100083China School of Chemical&Environmental Engineering China University of Mining&TechnologyBeijing 100083China School of Chemistry and Chemical Engineering Shaanxi Normal UniversityXi’an 710119China State Key Lab of Organic-Inorganic Composites Beijing University of Chemical TechnologyBeijing 100029China Key Laboratory of Fuel Cell Technology of Guangdong Province South China University of TechnologyGuangzhou 510641China Academy of Science&Technology China University of Petroleum(East China)Dongying 257061China

The construction of robust coupling catalysts for accelerating electrocatalytic oxygen reduction reaction(ORR)through the modulation of the electronic structure and local atomic configuration is critical but remains ***,we report a facile and effective isolation-polymerization-pyrolysis(IPP)strategy for high-precision synthesis of single-atomic Mn sites coupled with Fe_(3)C nanoparticles encapsulated in N-doped porous carbon matrixes(Mn SAs/Fe_(3)C NPs@NPC)catalyst derived from predesigned bimetallic Fe/Mn polyphthalocyanine(FeMn-BPPc)conjugated polymer networks by solid-phase reaction *** from the synergistic effects between the single-atomic Mn-N_(4)sites and Fe_(3)C NPs as well as the confinement effect of NPC,the Mn SAs/Fe_(3)C NPs@NPC catalyst exhibited excellent electrocatalytic activity and stability for *** assembled Znair battery displayed larger power density of 186 mW·cm^(−2)than that of Pt/C+Ir/C-based *** also exhibits excellent stability without obvious voltage change after 106 cycles with 36 *** in-situ Raman spectra with in-situ attenuated total reflectance surface-enhanced infrared absorption spectroscopy(ATR-SEIRAS)characterization results indicated that the Mn-N_(4)site as an active site for the O_(2)adsorption-activation process,which effectively facilitates the generation of key*OOH intermediates and*OH desorption to promote the multielectron reaction *** calculation reveals that the excellent electrocatalytic performance originates from the charge redistribution and the d orbital shift resulting from Mn-Fe bond,which buffers the activity of ORR through the electron reservoir capable of electron donation or *** work paves a novel IPP strategy for constructing high-performance coupling electrocatalyst towards the ORR for energy conversion devices.

关键词： single atom catalyst nanoparticles electrocatalyst oxygen reduction zinc-air battery

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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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