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Nonsolvent-Induced Electrospun Fibers with Crater-Like Surface and High-Loading Polytriphenylamine-Derived as a Flexible Cathode for Lithium-Ion Batteries

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SSRN 2023年

作者： Xiong, Yufeng Li, Yingjiang Hu, Zhengfei Sun, Zhengquan Cheng, Yiliang Zhang, Yang Dong, Lijie Center for Smart Materials and Devices State Key Laboratory of Advanced Technology for Materials Synthesis and Processing School of Materials Science and Engineering Wuhan University of Technology Wuhan430070 China

Fabricating electrodes simultaneously possessing remarkable flexibility, excellent mechanical properties, and high energy density remains a significant challenge in flexible lithium-ion batteries (LIBs). Herein, a series of flexible organic composite films were prepared with high-loading polytriphenylamine (PTPA) and the derivatives (PTPA-PO) as active material, along with carbon nanotubes (CNTs) serving as conductive filler. The fabrication employed the polyethylene oxide (PEO) assisted nonsolvent (or poor solvent) induced phase separation electrospinning (NIPSE) method. Subsequently, the fiber morphology and electrochemical applications of the flexible organic composite films were systematically studied. Notably, the 60% PTPA-PO/20% CNTs/PEO flexible electrode with a high-loading active material of 60 wt% exhibits a significant discharge capacity of 146.6 mAh·g-1 and a favorable discharge platform ~ 3.7 V vs. Li. Furthermore, the inherent flexibility of electrode contributes to efficient and stable transport of ions and electrons, resulting in a fine capacity retention of 93.3% after 100 cycles. The improvement of electrochemical performance can be rationalized by the unique internal conductive network and crater-like surface structure of the fibers formed through the NIPSE method. This work provides an efficient method to fundamentally improve the energy storage performance and flexibility of LIBs. © 2023, The Authors. All rights reserved.

关键词： Electrospinning

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Thermoelectric Energy Extraction in Motion Scenarios: Self-Powered Temperature and Pressure Detector in an Automobile Tire

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SSRN 2023年

作者： Yang, Dongwang Wang, Jiang Xing, Yubing Hu, Kai Lyu, Jianan Li, Junhao Liu, Yutian Xiao, Yani Yan, Yonggao Tang, Xinfeng State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China Nanostructure Research Center Wuhan University of Technology Wuhan430070 China

This study employs finite element simulation methods to meticulously analyze the temperature distribution within swiftly moving car tires to assess energy recovery possibilities. Results show that at 20 °C ambient temperature and a speed of 120 km/h, the maximum tire surface temperature due to friction and rubber deformation hysteresis reaches 91.2 °C. Additionally, a micro thermoelectric generator (micro-TEG) installed on the aluminum alloy wheel hub, functioning as a heat sink, demonstrates an effective temperature difference of 3.9 °C. When subjected to a temperature difference of 20 °C, the micro-TEG module exhibits open circuit voltage and maximum power of 1.47 V/1.41V and 12.06 mW/11.58 mW in the flat and curved states, respectively. To ensure module reliability, rigorous testing is conducted, including 10,000 cycles of bending, barometric shocking, and 20 cycles of temperature variations ranging from 0-100 °C. Remarkably, the module exhibits minimal alterations in internal resistance and open circuit voltage throughout the testing process. Additionally, the module is seamlessly integrated with energy management and Bluetooth signal transmission circuits (total weight: 8.96 g). During simulated car driving, the temperature and pressure signals received by the mobile phone software demonstrate high accuracy, with over 94% consistency compared to the measured results. © 2023, The Authors. All rights reserved.

关键词： Open circuit voltage

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Thermoelectric Energy Extraction in Motion Scenarios: Self-Powered Temperature and Pressure Detector in an Automobile Tire

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SSRN 2023年

关键词： Open circuit voltage

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In Situ Tin Doping to Enhance the Cycling Performance of 4.9 V LNMO Cathode Materials

In Situ Tin Doping to Enhance the Cycling Performance of 4.9...

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IEEE International Conference on Power and Energy Applications (ICPEA)

作者： Yan Li Jinqiao Du Zhaojie Liang Jie Tian Pei Wang Wen Luo Electric Power Scientific Research Institute Shenzhen Power Supply Bureau Co. Ltd Shenzhen China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan China

ISBN: (数字)9798350356113

ISBN: (纸本)9798350356120

LiNi 0.5 Mn 1.5 O 4 (LNMO) cathode material has the advantages of high energy density (650 Wh/kg), high discharge voltage (4.7 V vs Li+/Li), low raw material cost, low pollution, and high lithium ion transmission efficiency. It is a potential high power, low cost cobalt-free lithium-ion battery cathode material. However, the capacity decline of LNMO during high voltage charge and discharge processes leads to short cycle life, which limits its wide application and commercialization. To address this issue, this article uses in-situ Sn doping to enhance the cycle stability of LNMO. By uniformly mixing acetate salts in stoichiometric ratio and using one-step spray drying method to prepare undoped and Sn-doped LNMO cathode materials, this study systematically investigates the structural changes, morphological characteristics, and electrochemical performance before and after doping. The capacity retention rates of Sn-doped LNMO materials after 350 cycles at 0.7C are 93.5% and 94.5%, respectively, significantly higher than the undoped 80.8%, indicating that in-situ Sn doping can significantly enhance cycle performance. This study demonstrates that the LiNi 0.5 Mn 1.46 O 0.04 electrode prepared by spray drying method, with its simple and straightforward synthesis process and excellent electrochemical performance, has the potential to become a high-performance lithium-ion batteries cathode material.

关键词： Lithium-ion batteries Salt Electric potential Doping High-voltage techniques Voltage Lithium Ions Discharges (electric) Cathodes

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Mg-Based Micromotors with Motion Responsive to Dual Stimuli

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Research 2020年第1期2020卷 966-977页

作者： Kang Xiong Leilei Xu Jinwei Lin Fangzhi Mou Jianguo Guan State Key Laboratory of Advanced Technology for Materials Synthesis and Processing International School of Materials Science and EngineeringWuhan University of TechnologyWuhan 430070China

Mg-based micromotors have emerged as an extremely attractive artificial micro/nanodevice,but suffered from uncontrollable propulsion and limited motion lifetime,restricting the fulfillment of complex ***,we have demonstrated Mg-based micromotors composed of Mg microspheres asymmetrically coated with Pt and temperature-sensitive poly(N-isopropylacrylamide)(PNIPAM)hydrogel layers in *** can implement different motion behaviors stemming from the driving mechanism transformation when encountering catalyzed substrates such as H_(2)O_(2) and respond to both H_(2)O_(2) concentration and temperature in aqueous *** as-constructed Mg-based micromotors are self-propelled by Pt-catalyzed H_(2)O_(2) decomposition following the self-consuming Mg-H_(2)O *** this case,they could further generate bilateral bubbles and thus demonstrate unique self-limitation motion like hovering when the phase transformation of PNIPAM is triggered by decreasing temperature or when the H_(2)O_(2) concentration after permeating across the PNIPAM hydrogel layer is high enough to facilitate bubble *** work for the first time provides a stimuli-induced“hovering”strategy for self-propelled micromotors,which endows Mg-based micromotors with an intelligent response to the surroundings besides the significant extension of their motion lifetime.

关键词： transformation consuming attractive

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Large-scale manufacturing sulfide superionic conductor for advancing all-solid-state batteries

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Matter 2025年

作者： Wang, Shuo Lou, Chenjie Wu, Xinbin Lin, Jing Gautam, Ajay Li, Shenghao Huang, Jielei Cheng, Zhu Zhang, Shengnan Zhang, Xin Strauss, Florian Brezesinski, Torsten Luo, Guoqiang Tang, Mingxue Shen, Yang Lin, Yuanhua Nan, Ce-Wen Center of Smart Materials and Devices State Key Laboratory of Advanced Technology for Materials Synthesis and Processing School of Material Science and Engineering Wuhan University of Technology Wuhan430070 China Center for High Pressure Science and Technology Advanced Research Beijing100094 China State Key Laboratory of New Ceramics and Fine Processing School of Materials Science and Engineering Tsinghua University Beijing100084 China Kaiserstr. 12 Karlsruhe76131 Germany Department of Radiation Science and Technology Delft University of Technology JB Delft2629 Netherlands

Lithium argyrodites with high ionic conductivities are favorable solid electrolytes (SEs) for all-solid-state batteries (ASSBs). However, their low preparation efficiency and poor cycling performance hinder their large-scale applications. In this work, we demonstrate successful large-scale production (over 1 kg per batch for the first time) of Li5.5PS4.5Cl0.75Br0.75 (LPSCB) by fast dry mixing followed by annealing, which presents high room temperature ionic conductivities of 13 mS cm−1 for cold-pressed and 25 mS cm−1 for sintered pellets. Combining neutron powder diffraction and 6Li → 7Li tracer-exchange nuclear magnetic resonance (NMR) spectroscopy measurements, we show that intercage jumps frequently occur through the 48h-16e-48h pathway in LPSCB, promoting the overall lithium conduction. The assembled ASSBs using LPSCB and a LiNi0.83Co0.11Mn0.06O2 electrode can be cycled for over 2,500 cycles at a 0.5 C rate and 1,800 cycles at a 2 C rate without any capacity degradation. Our results will accelerate the commercialization of sulfide SE for ASSBs. © 2025 Elsevier Inc.

关键词： Neutron powder diffraction

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Designing polymer nanocomposites with high energy density using machine learning

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npj Computational Materials 2021年第1期7卷 999-1007页

作者： Zhong-Hui Shen Zhi-Wei Bao Xiao-Xing Cheng Bao-Wen Li Han-Xing Liu Yang Shen Long-Qing Chen Xiao-Guang Li Ce-Wen Nan State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Center of Smart Materials and DevicesWuhan University of TechnologyWuhanChina International School of Materials Science and Engineering Wuhan University of TechnologyWuhanChina Hefei National Laboratory for Physical Sciences at the Microscale Department of Physics and CAS Key Laboratory of Strongly-Coupled Quantum Matter Physics University of Science and Technology of China HefeiChina Department of Materials Science and Engineering The Pennsylvania State UniversityUniversity ParkPAUnited States School of Materials Science and Engineering State Key Lab of New Ceramics and Fine ProcessingTsinghua UniversityBeijingChina

Addressing microstructure-property relations of polymer nanocomposites is vital for designing advanced dielectrics for electrostatic energy ***,we develop an integrated phase-field model to simulate the dielectric response,charge transport,and breakdown process of polymer ***,based on 6615 high-throughput calculation results,a machine learning strategy is schemed to evaluate the capability of energy *** find that parallel perovskite nanosheets prefer to block and then drive charges to migrate along with the interfaces in x-y plane,which could significantly improve the breakdown strength of polymer *** verify our predictions,we fabricate a polymer nanocomposite P(VDF-HFP)/Ca_(2)Nb_(3)O_(10),whose highest discharged energy density almost doubles to 35.9 J cm^(−3) compared with the pristine polymer,mainly benefit from the improved breakdown strength of 853 MVm^(−1).This work opens a horizon to exploit the great potential of 2D perovskite nanosheets for a wide range of applications of flexible dielectrics with the requirement of high voltage endurance.

关键词： polymer energy perovskite

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Defects enriched hollow porous Co-N-doped carbons embedded with ultrafine CoFe/Co nanoparticles as bifunctional oxygen electrocatalyst for rechargeable flexible solid zinc-air batteries

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Nano Research 2021年第3期14卷 868-878页

作者： Zhao Lei Yangyang Tan Zeyi Zhang Wei Wu Niancai Cheng Runzhe Chen Shichun Mu Xueliang Sun College of Materials Science and Engineering Fuzhou UniversityFuzhou350108China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan430070China Department of Mechanical and Materials Engineering The University of Western OntarioLondonONN6A 5B9Canada

The construction and design of highly efficient and inexpensive bifunctional oxygen electrocatalysts substitute for noble-metal-based catalysts is highly desirable for the development of rechargeable Zn-air battery(ZAB).In this work,a bifunctional oxygen electrocatalysts of based on ultrafine CoFe alloy(4-5 nm)dispersed in defects enriched hollow porous Co-N-doped carbons,made by annealing SiO2 coated zeolitic imidazolate framework-67(ZIF-67)encapsulated Fe *** hollow porous structure not only exposed the active sites inside ZIF-67,but also provided efficient charge and mass *** strong synergetic coupling among high-density CoFe alloys and Co-N_(x) sites in Co,N-doped carbon species ensures high oxygen reduction reaction(ORR)and oxygen evolution reaction(OER)***-principles simulations reveal that the synergistic promotion effect between CoFe alloy and Co-N site effectively reduced the formation energy of from O^(*)to OH^(*).The optimized CoFe-Co@PNC exhibits outstanding electrocatalytic stability and activity with the overpotential of only 320 mV for OER at 10 mA·cm^(−2) and the half-wave potential of 0.887 V for ORR,outperforming that of most recent reported bifunctional electrocatalysts.A rechargeable ZAB constructed with CoFe-Co@PNC as the air cathode displays long-term cyclability for over 200 h and high power density(152.8 mW·cm^(−2)).Flexible solid-state ZAB with our CoFe-Co@PNC as the air cathode possesses a high open circuit potential(OCP)up to 1.46 V as well as good bending *** universal structure design provides an attractive and instructive model for the application of nanomaterials derived from MOF in the field of sustainable flexible energy applications device.

关键词： oxygen reduction reaction ultrafine CoFe alloy hollow porous carbons zeolitic imidazolate framework-67 Zn-air battery

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Tuning the dual-active sites of ZIF-67 derived porous nanomaterials for boosting oxygen catalysis and rechargeable Zn-air batteries

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Nano Research 2021年第7期14卷 2353-2362页

作者： Zeyi Zhang Yangyang Tan Tang Zeng Liyue Yu Runzhe Chen Niancai Cheng Shichun Mu Xueliang Sun College of Materials Science and Engineering Fuzhou UniversityFuzhou 350108China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Department of Mechanical and Materials Engineering University of Western OntarioLondonON N6A 5B9Canada

The rational control of the active site of metal-organic frameworks(MOFs)derived nanomaterials is essential to build efficient bifunctional oxygen reduction/evolution reaction(ORR/OER)***,through designing and constructing a Co_(3)O_(4)-Co heterostructure embedded in Co,N co-doped carbon polyhedra derived(Co_(3)O_(4)-Co@NC)from the in-situ compositions of ZIF-67 and cobalt nanocrystals synthesized by the strategy of in-situ NaBH4 reduction,the dual-active site(Co_(3)O_(4)-Co and Co-N_(x))is synchronously realized in a MOFs derived *** formed Co_(3)O_(4)-Co@NC shows excellent bifunctional electrocatalytic activity with ultra-small potential gap(ΔE=E_(j=10)(OER)–E_(1/2)(ORR))of 0.72 V,which surpasses the commercial Pt/C and RuO_(2) *** theory calculation results reveal that the excellent bifunctional electrocatalytic activity can be attributed to the charge redistribution of Co of Co-N_(x) induced by the synergistic effects of well-tuned active sites of Co_(3)O_(4)-Co nanoparticle and Co-N_(x),thus optimizing the rate-determining step of the desorption of O_(2)^(*)intermediate in ORR and OH^(*)intermediate in *** rechargeable Zn-air batteries with our bifunctional catalysts exhibit superior performance as well as high cycling *** simple-effective optimization strategy offers prospects for tuning the active site of MOF derived bifunctional catalyst in electrochemical energy devices.

关键词： dual-active sites bifunctional oxygen electrocatalysts metal−organic frameworks Zn-air batteries density functional theory(DFT)

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Sulfur-linked carbonyl polymer as a robust organic cathode for rapid and durable aluminum batteries

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Journal of Energy Chemistry 2021年第12期30卷 320-327,I0007页

作者： Liang Fang Limin Zhou Lianmeng Cui Peixin Jiao Qinyou An Kai Zhang Department of Energy and Materials Engineering Dongguk University-SeoulSeoul 04620Republic of Korea Key Laboratory of Advanced Energy Materials Chemistry(Ministry of Education) Engineering Research Center of High-efficiency Energy Storage(Ministry of Education)Renewable Energy Conversion and Storage Center(RECAST)College of ChemistryNankai UniversityTianjin 300071China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070HubeiChina Foshan Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong Laboratory Foshan 528200GuangdongChina

Rechargeable aluminum batteries are believed as a promising next-generation energy-storage system due to abundant low-cost Al sources and high volumetric specific *** Al-storage cathodes,however,are plagued by strong electrostatic interaction between host materials and carrier ions,leading to large overpotential and undesired cycling stability as well as sluggish ion diffusion ***,sulfur-linked carbonyl polymer based on perylene-3,4,9,10-tetracarboxylic dianhydride(PTCDA) as the cathode materials for ABs is proposed,which demonstrates a small voltage polarization(135 mV),a reversible capacity of 110 mAh g^(-1) at 100 mA g^(-1) even after 1200 cycles,and rapid Al-storage *** with PTCDA,the sulfide polymer possesses higher working voltage because of its lower LUMO energy level according to theoretical *** ordered carbonyl active sites in sulfide polymer contribute to the maximized material utilization and rapid ion coordination and dissociation,resulting in superior rate ***,the bridged thioether bonds endow the polysulfide with robust and flexible structure,which inhibits the dissolution of active materials and improves cycling *** work implies the importance of ordered arrangement of redox active moieties for organic electrode,which provides the theoretical direction for the structural design of organic materials applied in multivalent-ion batteries.

关键词： Aluminum batteries Organic materials Carbonyl polymer Electrochemical active sites Ordered arrangement

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