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Room Temperature synthesis of Vertically Aligned Amorphous Ultrathin NiCo-LDH Nanosheets Bifunctional Flexible Supercapacitor Electrodes

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Energy & Environmental materials 2024年第2期7卷 277-286页

作者： Kwadwo Asare Owusu Zhaoyang Wang Ali Saad Felix Ofori Boakye Muhammad Asim Mushtaq Muhammad Tahir Ghulam Yasin Dongqing Liu Zhengchun Peng Xingke Cai Institute for Advanced Study Shenzhen UniversityShenzhen 518060China College of Physics and Optoelectronics Shenzhen University3688 Nanhai BoulevardNanshan DistrictShenzhen 518060China School of Chemistry and Materials Science Hubei Engineering UniversityNo.272 Traffic AvenueXiaogan 432000China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyNo.122 Luoshi RoadWuhan 430070China Key Laboratory of Green Printing CAS Research Centre for Excellence in Molecular ScienceInstitute of Chemistry Chinese Academy of Sciences(ICCAS)Beijing 100190China College of Mechatronics and Control Engineering Shenzhen University3688 Nanhai BoulevardNanshan DistrictShenzhen 518050China

Developing a simple scalable method to fabricate electrodes with high capacity and wide voltage range is desired for the real use of electrochemical ***,we synthesized amorphous NiCo-LDH nanosheets vertically aligned on activated carbon cloth substrate,which was in situ transformed from Co-metal-organic framework materials nano-columns by a simple ion exchange process at room *** to the amorphous and vertically aligned ultrathin structure of NiCo-LDH,the NiCo-LDH/activated carbon cloth composites present high areal capacities of 3770 and 1480 mF cm^(-2)as cathode and anode at 2 mA cm^(-2),and 79.5%and 80%capacity have been preserved at 50 mA cm^(-2).In the meantime,they all showed excellent cycling performance with negligible change after>10000 *** fabricating them into an asymmetric supercapacitor,the device achieves high energy densities(5.61 mWh cm^(-2)and 0.352 mW cm^(-3)).This work provides an innovative strategy for simplifying the design of supercapacitors as well as providing a new understanding of improving the rate capabilities/cycling stability of NiCo-LDH materials.

关键词： amorphous nanosheets aqueous supercapacitor high volumetric/areal energy density NiCo-LDH room temperature synthesis

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A Rate-Dependent Peridynamic Model for the Dynamic Behavior of Ceramic materials

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Computer Modeling in Engineering & Sciences 2020年第7期124卷 151-178页

作者： Bufan Chu Qiwen Liu Lisheng Liu Xin Lai Hai Mei Department of Engineering Structure and Mechanics Wuhan University of TechnologyWuhan430070China Hubei Key Laboratory of Theory and Application of Advanced Materials Mechanics Wuhan430070China State Key Laboratory of Materials Synthesis and Processing Wuhan430070China

In this study,a new bond-based peridynamic model is proposed to describe the dynamic properties of ceramics under impact *** materials show pseudo-plastic behavior under certain compressive loadings with high strain-rate,while the characteristic brittleness of the material dominates when it is subjected to tensile *** this model,brittle response under tension,softening plasticity under compression and strain-rate effect of ceramics are considered,which makes it possible to accurately capture the overall dynamic process of *** enables the investigation of the fracture mechanism for ceramic materials,during ballistic impact,in more ***,a bond-force updating algorithm is introduced to perform the numerical simulation and solve the derived *** proposed model is then used to analyze the dynamic response of ceramics tiles under impact loading to assess its *** results of damage development in ceramic materials are calculated and compared with the experimental *** simulation results are consistent with the experiments,which indicates that the proposed rate-dependent peridynamic model has the capability to describe damage propagation in ceramics with good ***,based on a comparison between simulation and experimental results,it can be concluded that the damage results are in better agreement with experimental results than non-ordinary state-based peridynamic method.

关键词： Penetration ceramic peridynamics rate-dependency crack

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Polyoxometalated metal-organic framework superstructure for stable water oxidation

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Science (New York, N.Y.) 2025年第6745期388卷 430-436页

作者： Yue, Kaihang Lu, Ruihu Gao, Mingbin Song, Fei Dai, Yao Xia, Chenfeng Mei, Bingbao Dong, Hongliang Qi, Ruijuan Zhang, Daliang Zhang, Jiangwei Wang, Ziyun Huang, Fuqiang Xia, Bao Yu Yan, Ya State Key Laboratory of High Performance Ceramics and Superfine Microstructure Shanghai Institute of Ceramics Chinese Academy of Sciences Shanghai China School of Chemistry and Chemical Engineering State Key Laboratory of Materials Processing and Die & Mould Technology Key Laboratory of Material Chemistry for Energy Conversion and Storage (Ministry of Education) Hubei Key Laboratory of Material Chemistry and Service Failure Wuhan National Laboratory for Optoelectronics Huazhong University of Science and Technology (HUST) Wuhan China Center of Materials Science and Optoelectronics Engineering University of Chinese Academy of Sciences Beijing China School of Chemical Sciences University of Auckland Auckland New Zealand National Engineering Laboratory for Methanol to Olefins Dalian Institute of Chemical Physics Chinese Academy of Sciences Dalian China Shanghai Advanced Research Institute Chinese Academy of Sciences Shanghai Synchrotron Radiation Facility Shanghai China Center for High Pressure Science and Technology Advanced Research Shanghai China Key Laboratory of Polar Materials and Devices (MOE) Department of Electronics East China Normal University Shanghai China Multiscale Porous Materials Center Institute of Advanced Interdisciplinary Studies and School of Chemistry and Chemical Engineering Chongqing University Chongqing China College of Energy Material and Chemistry Inner Mongolia Key Laboratory of Low Carbon Catalysis Inner Mongolia University Hohhot China State Key Lab of Metal Matrix Composites School of Materials Science and Engineering Shanghai Jiao Tong University Shanghai China Center for Next-Generation Energy Materials and School of Chemical Engineering Sungkyunkwan University (SKKU) Seobu-ro Jangan-guGyeonggi-do Suwon South Korea

Stable, nonprecious catalysts are vital for large-scale alkaline water electrolysis. Here, we report a grafted superstructure, MOF@POM, formed by self-assembling a metal-organic framework (MOF) with polyoxometalate (POM). In situ electrochemical transformation converts MOF into active metal (oxy)hydroxides to produce a catalyst with a low overpotential of 178 millivolts at 10 milliamperes per square centimeter in alkaline electrolyte. An anion exchange membrane water electrolyzer incorporating this catalyst achieves 3 amperes per square centimeter at 1.78 volts at 80°C and stable operation at 2 amperes per square centimeter for 5140 hours at room temperature. In situ electrochemical spectroscopy and theoretical studies reveal that the synergistic interactions between metal atoms create a fast electron-transfer channel from catalytic iron and cobalt sites, nickel, and tungsten in the polyoxometalate to the electrode, stabilizing the metal sites and preventing dissolution.

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Ag-Pd Bimetallic Hollow Nanostructures with Tunable Compositions and Structures for the Reduction of 4-Nitrophenol

SSRN

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SSRN 2022年

作者： Ma, Wenjuan Zhang, Guimin Fu, Zhengyi School of Chemistry Chemical Engineering and Life Science Wuhan University of Technology Wuhan430070 China State Key Lab of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China

Bimetallic hollow nanostructures are of interest for high-performance nanocatalysis and utilization efficiency of noble metals. The paper reported a synthesis of Ag-Pd bimetallic hollow nano-hexagon with outer sizes of about 27 nm and wall thicknesses of 3 to 5 nm by galvanic replacement reaction coupling with co-reduction method using Ag nanospheres as sacrificial templates. Cetyltrimethylammonium bromide (CTAB) had double effect on controlling morphologies. It served as the capping agent to mediate the rate of dissolution and deposition on different planes by selectively absorption, meanwhile it provided Br - ion to involve in the reaction and promote the thermodynamics of the galvanic replacement. The compositions and structures of Ag-Pd bimetals could be finely tuned by changing the amount of palladium chloride acid (H 2 PdCl 4 ) while maintaining the volume of Ag seed templates. By comparison of the rate constant k m of 4-nitrophenol reduction reaction over different samples as catalyst, hollow bimetallic nano-hexagon with composition of AgPd 0.76 exhibited the highest catalytic activity because of high surface areas and synergy effect between two metal. © 2022, The Authors. All rights reserved.

关键词： Chlorine compounds

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Na doping and CeO2 surface modification enhancing the Li-rich Li1.2Mn0.54Ni0.13Co0.13O2 cathode material for lithium-ion battery

SSRN

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SSRN 2024年

作者： Li, Yu Feng, Xiang-Yu Ran, Mao-Jin Yuan, Man-Man Wei, Mei-Tong Wu, Liang Hu, Zhi-Yi Chen, Li-Hua Su, Bao-Lian State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China Wuhan University of Technology Wuhan430070 China School of Automotive Engineering Xiangyang Polytechnic 18 Longzhong Road Hubei Xiangyang441050 China University of Namur NamurB-5000 Belgium

Li-rich Mn-based layered oxides with high specific capacity and operating voltages become one of the most promising materials for lithium-ion batteries (LIBs). However, it still faces several issues on low initial coulombic efficiency, poor electronic conductivity and voltage fading due to oxygen release and transition metals rearrangement during cycling. In this study, Li1.2Mn0.54Ni0.13Co0.13O2 (LMR) cathode material with Na ion doping (LMNaR) and CeO2 surface modification (LMNaR@CeO2) is prepared to realize the synergistic modification effect. The doping of Na ions enlarges Li layer spacing to effectively promote the insertion and extraction of lithium ions, which makes the layered structure more stable to reduce the effect of phase transition. And the CeO2 surface modification restrains the side reactions between electrode and electrolyte, and stabilizes lattice oxygen and eases oxygen release. As a result, the LMNaR@CeO2 displays a specific capacity of 196 mAh·g-1 after 100 cycles at 0.5 C with a capacity retention of 94% and a merely voltage decay of 0.16 V, which are much better than the LMR with a specific capacity of 159.6 mAh·g-1 and only a 79% capacity retention. Our strategy here provides a feasible approach for the development of Li-rich Mn-based anode materials for long life LIBs. © 2024, The Authors. All rights reserved.

关键词： Lithium-ion batteries

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Major strategies for improving the performance of perovskite solar cells

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iEnergy 2023年第3期2卷 172-199页

作者： Lixiu Zhang Hang Li Kai Zhang Wenzhe Li Chuantian Zuo George Omololu Odunmbaku Jingde Chen Cong Chen Luozheng Zhang Ru Li Yuping Gao Baomin Xu Jiangzhao Chen Yongsheng Liu Yang Wang Yanlin Song Jianxin Tang Feng Gao Qing Zhao Yong Peng Mingzhen Liu Lei Tao Yuelong Li Zhimin Fang Ming Cheng Kuan Sun Dewei Zhao Yixin Zhao Shihe Yang Chenyi Yi Liming Ding Center for Excellence in Nanoscience(CAS) Key Laboratory of Nanosystem and Hierarchical Fabrication(CAS)National Center for Nanoscience and TechnologyBeijing 100190China State Key Laboratory of Power System Department of Electrical EngineeringTsinghua UniversityBeijing 100084China Shenzhen Graduate School Peking UniversityShenzhen 518055China School of Environmental Science and Engineering Shanghai Jiao Tong UniversityShanghai 200240China College of Materials Science and Engineering&Engineering Research Center of Alternative Energy Materials&Devices Sichuan UniversityChengdu 610065China School of Energy&Power Engineer-ing Chongqing UniversityChongqing 400044China Institute for Energy Research Jiangsu UniversityZhenjiang 212013China Institute of New Energy Technology Department of Electronic EngineeringCollege of Information Science and TechnologyJinan UniversityGuangzhou 510631China Institute of Functional Nano&Soft Materials(FUNSOM) Soochow UniversitySuzhou 215123China Department of Materials Science and Engineering Southern University of Science and TechnologyShenzhen 518055China College of Optoelectronic Engineering Chongqing UniversityChongqing 400044China College of Chemistry Nankai UniversityTianjin 300071China Institute of Chemistry Chinese Academy of SciencesBeijing 100190China State Key Lab for Mesoscopic Physics and Frontiers Science Center for Nano-optoelec-tronics School of PhysicsPeking UniversityBeijing 100871China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China School of Materials and Energy University of Electronic Science and Technology of ChinaChengdu 611731China Institute of Photoelectronic Thin Film Devices and Technology Nankai UniversityTianjin 300350China School of Materials Science and Engineering Shaanxi Normal UniversityXi’an 710119China

Metal halide perovskite solar cell(PSC)has successfully distinguished itself in optoelectronic field by virtue of the sharp rise in power conversion efficiency over the past *** remarkable efficiency breakthrough at such a fast speed can be mainly attributed to the comprehensive study on film deposition techniques,especially the effective management of surface and interfacial defects in recent ***,we summarized the current trends in performance enhancement for PSCs,with a focus on the generally applicable strategies in high-performance works,involving deposition methods,compositional engineering,additive engineering,crystallization manipulation,charge transport material selection,interfacial passivation,optical coupling effect and constructing tandem solar *** directions and perspectives are also provided.

关键词： Perovskite solar cells efficiency improvement strategies milestones

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Development of innovative and green adsorbents for in situ cleanup of fluoride-polluted groundwater: Mechanisms and field-scale studies

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Chemosphere 2024年 350卷 141035页

作者： Ou, Jiun-Hau Wang, Chih-Chieh Verpoort, Francis Chien, Chih-Ching Zhong, Hua-Bin Kao, Chih-Ming Institute of Environmental Engineering National Sun Yat-Sen University Kaohsiung Taiwan Hershey Environmental Technology Corp. Ltd. Kaohsiung Taiwan State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan China Graduate School of Biotechnology and Bioengineering Yuan Ze University Chung-Li City Taoyuan Taiwan

In this study, the magnesium oxide (MgO)-based adsorbents [granulated MgO aggregates (GA-MgO) and surface-modified MgO powder (SM-MgO)] were developed to remediate a fluoride-contaminated groundwater site. Both GA-MgO and SM-MgO had porous, spherical, and crystalline structures. Diameters for GA-MgO and SM-MgO were 1–1.7 mm and 1–10 μm, respectively. The pseudo second-order dynamic adsorption and the Freundlich isotherm could be applied to express the chemical adsorption phenomena. The monolayer adsorption was the dominant mechanism at the initial adsorption period. During the latter part of fluoride adsorption, the multilayer adsorption became the dominant mechanism for fluoride removal from the water phase, which also resulted in the increased adsorption capacity. Higher hydroxide, phosphate, and carbonate concentrations caused a decreased fluoride removal efficiency due to the competition of sorption sites between fluoride and other anions with similar electronic properties. Fluoride removal mechanism using GA-MgO and SM-MgO as the adsorbents was mainly carried out by the chemical adsorption. Reaction paths contained two main processes: (1) formation of magnesium hydroxide after the reaction of MgO with water, and (2) the hydroxyl group of the magnesium hydroxide was replaced by fluoride ions to form magnesium fluoride precipitation. Results from column tests show that up to 61 and 73% of fluoride removal (initial fluoride concentration = 9.3 mg/L) could be obtained after 50 pore volumes of groundwater pumping with GA-MgO and SM-MgO injection, respectively. The GA-MgO system could be applied to contain and remediate fluoride-contaminated groundwater, and SM-MgO could be applied as an immediate fluoride removal alternative to achieve a rapid pollutant removal for emergency responses. Up to 71% of fluoride removal (fluoride concentration = 10.8 mg/L) could be obtained with GA-MgO injection after 30 days of operation. The developed GA-MgO system is a potential and g

关键词： Magnesia

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Na Doping and Ceo2 Coating Enhancing the Li-Rich Li1.2mn0.54ni0.13co0.13o2 Cathode Material for Lithium-Ion Battery

SSRN

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SSRN 2024年

作者： Li, Yu Feng, Xiang-Yu Ran, Mao-Jin Yuan, Man-Man Peng, Yan Luo, Bi-Cheng Wei, Mei-Tong Wu, Liang Hu, Zhi-Yi Chen, Li-Hua Su, Bao-Lian State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China Wuhan University of Technology Wuhan430070 China School of Automotive Engineering Xiangyang Polytechnic 18 Longzhong Road Hubei Xiangyang441050 China University of Namur NamurB-5000 Belgium

Li-rich Mn-based layered oxides with high specific capacity (>250 mAh·g-1) and operating voltages become one of the most promising materials for lithium-ion batteries (LIBs). However, it still faces several issues on low initial coulombic efficiency, poor electronic conductivity and voltage fading due to oxygen release and transition metals rearrangement during cycling. In this study, Li1.2Mn0.54Ni0.13Co0.13O2 (LMR) cathode material with Na ion doping (LMNaR) and surface CeO2 coating (LMNaR@CeO2) is successfully prepared via a simple co-precipitation and wet chemical to realize the synergistic modification effect. On one hand, the doping of Na ions enlarges Li layer spacing to effectively promote the insertion and extraction of lithium ions. Meanwhile, due to the larger radius of Na ions, the layered structure becomes more stable, thus reducing the effect of phase transition. On the other hand, the CeO2 coating layer restrains the side reaction between electrode and electrolyte, and stabilizes lattice oxygen and eases oxygen release. The electrochemical results illustrate that the LMNaR@CeO2 exhibits outstanding electrochemical capabilities. Notably, it displays a specific capacity of 196 mAh·g-1 after 100 cycles at 0.5 C with a capacity retention of 94% and a merely voltage decay of 0.16 V, which are much better than the LMR with a specific capacity of 159.6 mAh·g-1 and only a 79% capacity retention. Our strategy here provides a feasible approach for the development of Li-rich Mn-based anode materials for long life LIBs. © 2024, The Authors. All rights reserved.

关键词： Lithium-ion batteries

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Three-Dimensional Porous Polyimide Anode For High-Rate Lithium Ion Batteries

SSRN

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SSRN 2023年

作者： Zhang, Qiuyitong Wei, Zijie Xu, Yuexin Lv, Ning Li, Hanyang Zhao, Xue Tian, 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 Xupu Central Primary School Yangzhou211400 China

Polymeric electrode materials suffer from poor electrical conductivity and slow transport kinetics, especially poor performance at high current density. Herein, a polyimide electrode structure with 3D ordered interconnected gradient pores is proposed for improving the lithium ion transport efficiency. The homogeneous mixed PMTA-PMMA composite is prepared by a simple one-pot method, and then the PMMA (polymethyl methacrylate) spherical porogenic agent is removed from it while synthesizing the polyimide material at high temperature to form a low curvature gradient pore structure. The large pores in the electrode can enhance the ion transport ability and improve the electrolyte infiltration rate, and the small pores can improve the active specific surface area and guide the deposition of lithium ions. The high specific capacity of 907mAh/g can be maintained even after 1000 cycles at 5A/g, which is about 3 times of the specific capacity of un-pored electrode material. This porous material with high active area and porosity is a potential electrode candidate for ultra-fast charging and discharging in lithium ion batteries, with high specific capacity and excellent cycling performance. © 2023, The Authors. All rights reserved.

关键词： Polyimides

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Strongly Enhancing the Energy Storage Properties and Stability of Amorphous BaTiO3 Thin Films via Ions Doping

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SSRN 2024年

作者： Chang, Ruiling Yao, Zhonghua Xing, Yutong Wang, Jun Hao, Hua Cao, Minghe Liu, Hanxing State Key Laboratory of Advanced Technology for Materials Synthesis and Processing School of Material Science and Engineering Wuhan University of Technology Wuhan430070 China International School of Material Science and Engineering Wuhan University of Technology Wuhan430070 China Sanya Science and Education Innovation Park of Wuhan University of Technology Sanya572000 China

Amorphous thin films with high power density and breakdown strength satisfy the needs of advanced power electronic systems. Nonetheless, improving the energy storage density of amorphous films is critical for addressing the growing demand for electricity. We apply high spontaneous polarization BaTiO3 as the main component to make (1-x)Ba(Ti0.99Mn0.02)O3-xBiFeO3((1-x)BTM-xBF) thin films. Doping BiFeO3 (BF) synergistically boosts polarization. The introduction of amorphous phases and Mn ions enhances the breakdown strength. The results demonstrate that, at x=0.10, the film can achieve both a high efficiency of 80.3% and an excellent energy storage density of 111.3 J cm-3. Moreover, the film has a strong thermal stability within a broad range of 20°C ~ 160°C, as well as the cycling reliability is as high as 105 times. The present study offers a practical approach to develop film capacitors with outstanding energy storage capabilities. © 2024, The Authors. All rights reserved.

关键词： Amorphous films

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