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Simpler and Greener Preparation of An In-Situ Polymerized Polyimide Anode for Lithium Ion Batteries

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SSRN 2023年

作者： Zhang, Qiuyitong Xu, Yuexin Lv, Ning Li, Hanyang Wei, Zijie Tiana, Tian Wang, Yadong Tang, Haolin State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China Foshan Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong Laboratory Xianhu Hydrogen Valley Foshan528200 China

A simplified and greener procedure for in-situ obtaining polyimide anode materials for lithium-ion battery electrodes is developed. The combined polyimide material synthesis and electrode preparation reduces the number of processing steps and treatment duration and decreases the energy required for heat treatment, solvent evaporation, and organic solvent use. More importantly, polymerization in situ on the electrode surface render the polyimide particles a sea urchin-like structure, leading to fast electrochemical kinetics, and significant improvement in discharge capacity and cycling performance compared with materials obtained using traditional procedures. Specific capacities of 1870 mAh g-1 and 2277 mAh g-1 at 30℃ and 60℃, respectively, are obtained. A capacity of 1774 mAh g-1 is retained after 500 cycles at high current density of 1000 mA g-1 at 60℃. This new preparation process not only simplifies the preparation process and makes it greener, but also significantly improves the battery performance, providing new possibilities for the preparation of high-performance low-cost lithium-ion battery electrodes. © 2023, The Authors. All rights reserved.

关键词： Solvents

Flexible and highly-sensitive pressure sensor based on controllably oxidized MXene

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InfoMat 2022年第9期4卷 60-71页

作者： Yanan Ma Yongfa Cheng Jian Wang Si Fu Mengjun Zhou Yue Yang Baowen Li Xin Zhang Ce-Wen Nan State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Center of Smart Materials and Devices&International School of Materials Science and EngineeringWuhan University of TechnologyWuhanChina School of Mathematics Physics and Optoelectronic EngineeringHubei University of Automotive TechnologyShiyanChina Center for Nanoscale Characterization&Devices(CNCD) Wuhan National Laboratory for Optoelectronics(WNLO)Huazhong University of Science and Technology(HUST)WuhanChina Information Materials and Intelligent Sensing Laboratory of Anhui Province Key Laboratory of Structure and Functional Regulation of Hybrid Materials of Ministry of EducationInstitutes of Physical Science and Information TechnologyAnhui UniversityHefeiChina State Key Lab of New Ceramics and Fine Processing School of Materials Science and EngineeringTsinghua UniversityBeijingChina

Conductive Ti_(3)C_(2)T_(x)MXenes have been widely investigated for the construction of flexible and highly-sensitive pressure *** the inevitable oxidation of solution-processed MXene has been recognized,the effect of the irreversible oxidation of MXene on its electrical conductivity and sensing properties is yet to be ***,we construct a highly-sensitive and degradable piezoresistive pressure sensor by coating Ti_(3)C_(2)T_(x)MXene flakes with different degrees of in situ oxidation onto paper substrates using the dipping-drying *** situ oxidation can tune the intrinsic resistance and expand the interlayer distance of MXene *** partially oxidized MXene-based piezoresistive pressure sensor exhibits a high sensitivity of 28.43 kPa^(-1),which is greater than those of pristine MXene,over-oxidized MXene,and state-of-the-art paper-based pressure ***,these sensors exhibit a short response time of 98.3 ms,good durability over 5000 measurement cycles,and a low force detection limit of 0.8 ***,MXene-based sensing elements are easily degraded and environmentally *** MXene-based pressure sensor shows promise for practical applications in tracking body movements,sports coaching,remote health monitoring,and human–computer interactions.

关键词： adjustable sensitivity in situ oxidation interlayer distance MXene pressure sensor

Light tuning CO/H_(2)composition on Ag:Unraveling CO_(2)mass transfer and electron-phonon coupling in plasmon-enhanced electrocatalysis

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Nano Research 2025年第1期18卷 173-185页

作者： Rui Lin Dong Fan Luca MBerger Thomas Possmayer Yu Zhou Jiexin Zhu Xingbao Chen Wen Luo Lars Allmendinger Andreas Tittl Leonardo de Souza Menezes Guillaume Maurin Shihe Yang and Stefan AMaier Nanoinstitute Munich Faculty of PhysicsLudwig-Maximilians-Universität München80539 MunichGermany Institut Charles Gerhardt Montpellier UMR 5253 CNRS ENSCM UniversitéMontpellierPlace E.Bataillon34090 MontpellierFrance Guangdong Provincial Key Lab of Nano-Micro Material Research School of Advanced MaterialsPeking University Shenzhen Graduate SchoolShenzhen 518055China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Faculty of Chemistry and Pharmacy Ludwig-Maximilians-Universität München81377 MunichGermany Departamento de Física Universidade Federal de Pernambuco50670-901 Recife-PEBrazil School of Physics and Astronomy Monash University Clayton CampusMelbourneVictoria 3800Australia Department of Physics Imperial College LondonSW72AZ LondonUK

Plasmon-enhanced electrocatalysis(PEEC)is an emerging approach to mitigate CO_(2)*** mechanisms behind CO_(2)adsorption and reduction at the catalyst-electrolyte interface in PEEC still need to be further ***,we employ a well-defined Ag nanostructure to elucidate these pivotal *** shining light with wavelengths of 625,525,405 nm on Ag,an adjustable CO/H_(2)ratio from 35 to 1 can be *** reaction pathway changing under plasmonic excitation does not originate from the lowered CO_(2)mass transfer in the vicinity of Ag,as the electrochemical quartz crystal microbalance results unravel that a slightly elevated temperature in bulk electrolyte caused by light irradiation cannot weaken the CO_(2)adsorption at the Ag catalyst-electrolyte *** calculations reveal that optical excitation towards shorter wavelengths leads to a progressive lowered energy barrier for H_(2)formation together with an enhanced energy barrier for^(*)COOH *** thermodynamically suppressed,CO_(2)reduction can still be improved kinetically by optimizing the excitation wavelength and intensity,being accompanied with the enhanced *** absorption spectroscopy results further correlate the higher photocurrent with a prolonged electron-phonon coupling time,verifying that the improvement of CO_(2)reduction kinetics in PEEC can be realized by hot electron harnessing.

关键词： plasmonic catalysis photoelectrochemical CO_(2)reduction CO/H_(2)ratio hot electron generation electronphonon coupling thermal effect

Polyphenol Synergistic Cerium Oxide Surface Engineering Constructed Core-Shell Nanostructures as Antioxidants for Durable and High-Performance Proton Exchange Membrane Fuel Cells

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SSRN 2023年

作者： Tang, Haolin Zhao, Shengqiu Liao, Yucong Wang, Rui Liu, Guoliang Zhang, Haining State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China Foshan Xianhu Laboratory The Advanced Energy Science and Technology Guangdong Laboratory Xianhu Hydrogen Valley Foshan528200 China

The chemical degradation of proton exchange membranes (PEMs) suffering from radical attack is a crucial issue in the development of proton exchange membrane fuel cells (PEMFCs), while incorporating cerium oxide (CeO2) nanoparticles (NPs) with regenerative redox properties to eliminate radicals could effectively alleviate degradation. However, the low stability and restricted activity of CeO2 in the PEMFC operating condition and the poor compatibility with PEM due to CeO2 agglomeration stimulate the urgency for structural modulation of CeO2. Herein, polyphenols surface functionalized CeO2 core-shell structure (CeO2@TP) were constructed via assembling oxidation-induced coupling tea polyphenols (TP) on CeO2 NPs. The TP oligomeric shell as a protective layer enhances the stability of CeO2, mitigating radical scavenging activity degradation and improving compatibility with PEMs. Gratifyingly, the phenolic hydroxyl-rich reductive TP oligomeric shell accelerates the regeneration of Ce(IV) to Ce(III), increasing the proportion of Ce(III) and oxygen vacancies on the CeO2 surface, thus boosting antioxidation efficiency. As a result, the CeO2@TP-based PEMs exhibited an OCV decay rate of 0.22 mV h-1, a maximum power density of 1.06 W cm-2, an H2 crossover value of 2.18 mA cm-2, thickness retention (91.1%), and negligible Ce migration after 404 hours of accelerated degradation testing. © 2023, The Authors. All rights reserved.

关键词： Oligomers

Boosting the Antioxidant Efficiency of Ce(Iii)-Based Organometallic Complexes Via Ion-Limited Domain and Electronic Structure Modulation Towards Robust Proton Exchange Membrane Fuel Cells

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SSRN 2023年

作者： Zhao, Shengqiu Liao, Yucong Wang, Rui Li, Hao Zhang, Haining Tang, Haolin State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China Foshan Xianhu Laboratory The Advanced Energy Science and Technology Guangdong Laboratory Xianhu Hydrogen Valley Foshan528200 China

Ce-based radical scavengers, including free Ce3+, are highly efficient radical scavengers with rapid and regenerative redox properties that can enhance the chemical durability of prton exchange membranes (PEMs). However, during the proton exchange membrane fuel cell (PEMFC) operation, water-soluble free Ce3+ ions in PEMs irreversibly migrate away and poison the proton-conducting ion clusters, leading to a decline in PEMFC output power. Herein, organometallic complexes of Ce3+ ions (Ce/HMCRE) derived by Ce3+ ions coordinating with 2-hydroxymethyl-15-crown-5 ether (HMCRE) ligands were utilized as FRS for improving the stability of PEMs. Owing to the coordination between the crown ether oxygen atom of the ligand and the Ce3+, the migration of Ce3+ and the adverse interactions among Ce3+ ions with the sulfonic group of PEM was inhibited. Meanwhile, the formation of coordination bonds allows the central Ce3+ ion to accept electrons on the ligand oxygen atom, thus enhancing the antioxidant efficiency of Ce/HMCRE. Gratifyingly, the hydrogen bonding between the hydroxymethyl group of the HMCRE ligand and the ether oxygen atom on the side chain of the perfluorosulfonic acid (PFSA) matrix also contributes to anchoring the Ce/HMCRE complex and mitigating its interference with ion clusters of PEM. Consequently, the Ce/HMCRE-based hybrid PEMs demonstrated an OCV decay rate of 0.45 mV h-1, a maximum power density of 1.07 W cm-2, an H2 crossover value of 2.41 mA cm-2, a thickness retention of 92% after 150 hours of accelerated degradation testing. © 2023, The Authors. All rights reserved.

关键词： Ligands

Flexible three-dimensional-networked iron vanadate nanosheet arrays/carbon cloths as high-performance cathodes for magnesium ion batteries

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Science China Materials 2022年第8期65卷 2197-2206页

作者： Han Tang Chunli Zuo Fangyu Xiong Cunyuan Pei Shuangshuang Tan Ping Luo Wei Yang Qinyou An Liqiang Mai State Key Laboratory of Advanced Technology for Materials Synthesis and Processing International School of Materials Science and EngineeringWuhan University of TechnologyWuhan 430070China Hubei Provincial Key Laboratory of Green Materials for Light Industry Collaborative Innovation Center of Green Light-Weight Materials and ProcessingSchool of Materials and Chemical EngineeringHubei University of TechnologyWuhan 430070China Foshan Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong Laboratory Foshan 528200China

Owing to their safety and low cost,magnesium ion batteries(MIBs)have attracted much attention in recent ***,the sluggish diffusion dynamics of magnesium ions hampers the search for appropriate cathode materials with excellent electrochemical ***,we design and synthesize a novel flexible three-dimensional-networked composite of iron vanadate nanosheet arrays/carbon cloths(3 D FeVO/CC)as a binder-free cathode for *** to bare FeVO nanosheets,the 3 D binder-free electrode with designed architecture enables a full range of electrochemical potential,including a high specific capacity of270 mA h g^(-1) and an increased life span(over 5000 cycles).Such achievable high-density energy originates from the synergistic optimization of electron and ion kinetics,while the durability benefits from the robust structure that prevents degradation in *** single-phase reaction mechanism of FeVO in the magnesium ion storage process is also explored by in-situ X-ray diffraction and Raman ***,a flexible MIB pouch cell(3 D FeVO/CCIMgNaTi_(3)O_(7)) is assembled and exhibits practical application *** work verifies that 3 D FeVO/CC is a potential candidate cathode material that can satisfy the requirements of highperformance *** also opens a new avenue to improve the electrochemical performance of cathode materials for MIBs.

关键词： iron vanadate nanosheet arrays flexibility cathode materials magnesium ion batteries

Confined Tuning of the Charge Distribution of Pt Electrocatalyst for Reinforcing Anti-Poisoning Ability: Toward Efficient Separation of Hydrogen from Gases Containing Ammonia

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SSRN 2023年

作者： Jin, Changqing Wu, Fanglin Tang, Haibo Pan, Hongfei Chen, Zhida Wang, Rui Meng, Zihan Li, Junsheng Tang, Haolin State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China Foshan Xianhu Laboratory of the Advanced Energy Science Technology Guangdong Laboratory Xianhu Hydrogen Valley Foshan528200 China

The development of catalysts for hydrogen oxidation reaction (HOR) with enhanced resistance to ammonia poisoning is an important factor in the practical application of hydrogen electrochemical purification devices (HEPDs). This paper reports on the creation of a highly active and anti-ammonia HOR catalyst developed by tuning the charge distribution of the support material through nitrogen-doping of carbon. The nitrogen-doped carbon-supported platinum catalyst (Pt-N2/KB, 2.03 wt.% Pt) achieves a high mass activity and exchange current density of 2788 mA mgpt-1 and 1020 mA mgpt-1, respectively, which are 5.4 and 4.7 times higher than that of the comm. 20% Pt/C. The Pt-N2/KB catalyst also displays a lower percentage of current decay and enhanced electrochemical stability, indicating superior anti-ammonia toxicity in the tests with HEPD. Density functional theory (DFT) calculations reveal that the hydrogen adsorption free energy (ΔGH*) on the surface of Pt-N2/KB is close to zero and has a lower ammonia adsorption energy, thus accounting for its superior HOR activity and anti- ammonia poisoning ability. Consequently, this work facilitates the implementation of HOR catalysts for anti-ammonia poisoning in the HEPDs, thus accelerating the advancement of ammonia cracking for hydrogen production. © 2023, The Authors. All rights reserved.

关键词： Ammonia

Hierarchical Microstructure and Strengthening Mechanism of Haynes 188 Alloy Manufactured by Laser Powder Bed Fusion

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SSRN 2022年

作者： Liu, Yang Huang, Zhifeng Zhang, Chi Lu, Jiaqi Ouyang, Ni Shen, Qiang Chen, Fei State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China

Co and Ni superalloys have been widely used in aerospace. Abundant studies have been focused on additive manufacturing of Ni superalloys. However, the equally important Co superalloy has less been fabricated by additive manufacturing. In this work, Haynes 188 alloy, a kind of Co-based superalloy, is fabricated by using laser powder bed fusion. The microstructure and mechanical properties before and after a stress relief treatment of the additive manufactured Haynes 188 alloys are investigated in detail. For as-built alloys without stress relief treatment, the thermodynamic modeling predicts that a phase of M 6 C exists in the specimen, which is confirmed by a TEM EDS mapping result. Arrayed stacking faults, dislocations, and M 6 C precipitations are widely found inside grains of the specimen without stress relief treatment. The yield strength and elongation of the specimen without stress relief treatment are 645 MPa and 57.3%, respectively. For the specimen with stress relief treatment, the dislocation density is reduced, the carbide precipitations are dissolved into the matrix, and stacking faults are arrayed near grain boundaries. As a result, the yield strength slightly decreases to 485 MPa but the elongation increases to 68.1%. The mechanical properties of fabricated Haynes 188 alloys in this work are superior to that of the published Ni or Co superalloys. This work provides an effective method to improve the mechanical properties of Co superalloys by additive manufacturing, which is important for the development of high-performance superalloys and their manufacturing methods. © 2022, The Authors. All rights reserved.

关键词： Superalloys

界面工程实现Au@MoS_(2)核壳异质结在等离激元学和光电子学领域卓越的热载流子输运动力学

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Science China Materials 2023年第10期66卷 3931-3940页

作者：刘然朱翔宇刘盛洪欧阳德才马小茜夏芳芳余一梦张悍吴劲松刘世元梁文锡李渊翟天佑 State Key Laboratory of Materials Processing and Die&Mould Technology School of Materials Science and EngineeringHuazhong University of Science and TechnologyWuhan 430074China Wuhan National Laboratory for Optoelectronics Huazhong University of Science and TechnologyWuhan 430074China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Nanostructure Research CenterWuhan University of TechnologyWuhan 430070China School of Engineering and Materials Science Queen Mary University of LondonMile End RoadLondonE14NSUK State Key Laboratory of Digital Manufacturing Equipment and Technology School of Mechanical Science and EngineeringHuazhong University of Science and TechnologyWuhan 430074China Shenzhen Huazhong University of Science and Technology Research Institute Shenzhen 518057China

贵金属和二维半导体构建的异质结为等离激元纳米结构产生的热载流子提供了独特的电荷传输路径,有望应用于各种等离激元和光电子器件.然而,传统异质结构的电荷转移速度和效率通常受限于有限的界面面积和不可避免的界面污染.本文中,具有... 详细信息

贵金属和二维半导体构建的异质结为等离激元纳米结构产生的热载流子提供了独特的电荷传输路径,有望应用于各种等离激元和光电子器件.然而,传统异质结构的电荷转移速度和效率通常受限于有限的界面面积和不可避免的界面污染.本文中,具有原子级清洁和较大接触界面的新型Au@MoS_(2)核壳异质结构能够实现超快和高效的热电子转移.飞秒瞬态吸收光谱研究表明,Au@MoS_(2)中从金纳米颗粒到MoS_(2)的热电子注入时间常数小于244 fs,而机械转移方法制备的Au/MoS_(2)对照样品的热电子注入时间常数为493 fs,同时,电荷转移效率从Au/MoS_(2)的3.33%提升至Au@MoS_(2)的25.3%.开尔文探针力显微镜和离散偶极近似研究进一步证明了上述结果,明显改善的电荷转移归因于原子级清洁和完全封装的异质结界面.这项研究提供了贵金属-二维半导体异质结构内固有电荷转移的基本理解,从而展现了Au@MoS_(2)这一新型异质结结构在等离激元和光电子器件中的应用前景.

关键词： 2D materials MoS_(2) heterostructures optoelectronics plasmonics