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Layered manganese phosphorus trisulfides for high-performance lithium-ion batteries and the storage mechanism

Carbon Energy 2023年第3期5卷 160-169,170,171页

作者： Hailin Shen Yueling Cai Zhongtao Ma Peng Wang Bingkun Guo Jipeng Cheng Qianqian Li Hongtao Wang Zhongyuan Liu Anmin Nie Jinsong Wu Materials Genome Institute Shanghai UniversityShanghaiChina Shanghai Key Laboratory of Mechanics in Energy Engineering School of Mechanics and Engineering ScienceShanghai Institute of Applied Mathematics and MechanicsShanghai UniversityShanghaiChina State Key Laboratory of Silicon Materials School of Materials Science and EngineeringZhejiang UniversityHangzhouChina Center for X‐mechanics Zhejiang UniversityHangzhouChina State Key Laboratory of Metastable Materials Science and Technology Center for High Pressure ScienceYanshan UniversityQinhuangdaoChina State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhanChina Nanostructure Research Center Wuhan University of TechnologyWuhanChina

Although advanced anode materials for the lithium-ion battery have been investigated for decades,a reliable,high-capacity,and durable material that can enable a fast charge remains ***,we report that a metal phosphorous trichalcogenide of MnPS_(3)(manganese phosphorus trisulfide),endowed with a unique and layered van der Waals structure,is highly beneficial for the fast insertion/extraction of alkali metal ions and can facilitate changes in the buffer volume during cycles with robust structural *** few-layered MnPS_(3)anodes displayed the desirable specific capacity and excellent rate chargeability owing to their good electronic and ionic *** assembled as a half-cell lithium-ion battery,a high reversible capacity of 380 mA h g^(−1)was maintained by the MnPS_(3)after 3000 cycles at a high current density of 4 A g^(−1),with a capacity retention of close to or above 100%.In full-cell testing,a reversible capacity of 450 mA h g^(−1)after 200 cycles was maintained as *** results of in-situ TEM revealed that MnPS_(3)nanoflakes maintained a high structural integrity without exhibiting any pulverization after undergoing large volumetric expansion for the insertion of a large number of lithium *** kinetics of lithium-ion diffusion,stable structure,and high pseudocapacitance contributed to their comprehensive performance,for example,a high specific capacity,rapid charge-discharge,and long ***_(3)is thus an efficient anode for the next generation of batteries with a fast charge/discharge capability.

关键词： cyclic stability in‐situ TEM MnPS3 pseudocapacitance rate performance

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Achieving better aqueous rechargeable zinc ion batteries with heterostructure electrodes

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Nano Research 2021年第9期14卷 3174-3187页

作者： Buke Wu Wen Luo Ming Li Lin Zeng Liqiang Mai State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Department of Mechanical and Energy Engineering Southern University of Science and TechnologyShenzhen 518055China Department of Physics School of ScienceWuhan University of TechnologyWuhan 430070China Guangdong Provincial Key Laboratory of Energy Materials for Electric Power Southern University of Science and TechnologyShenzhen 518055China Key Laboratory of Energy Conversion and Storage Technologies(Southern University of Science and Technology) Ministry of EducationShenzhen 518055China Foshan Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong Laboratory Xianhu hydrogen ValleyFoshan 528200China

Aqueous rechargeable zinc ion batteries(ARZIBs)have received unprecedented attention owing to the low cost and high-safety ***,their further development and application are hindered by the issues of electrodes such as cathode dissolution,zinc anode dendrite,passivation,as well as sluggish reaction *** heterostructure electrodes is a powerful method to improve the electrochemical performance of electrodes by grafting the advantages of functional materials onto the active *** this review,various modified heterostructure electrodes with optimized electrochemical performance and wider applications are ***,the synergistic effect between active materials and functional materials are also in-depth *** specific modification methods are divided into interphase modification(electrode-electrolyte interphase and electrode-current collector interphase)and structure ***,the conclusion and future perspective on the optimization mechanism of functional materials,and the cost issue of practical heterostructure electrodes in ARZIBs are also *** is expected that this review can promote the further development of ARZIBs towards practical utility.

关键词： zinc ion battery heterostructure electrodes interphase modification structure optimization

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Change in elastic properties during room-temperature aging in body-centered cubic Mg-Li and Mg-Li-Al single crystals

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Journal of Materials Science & technology 2022年第14期109卷 49-53页

作者： Ruxia Liu Shota Higashino Koji Hagihara Lianmeng Zhang Tohru Sekino Masakazu Tane SANKEN(The Institute of Scientific and Industrial Research) Osaka University8-1 MihogaokaIbarakiOsaka 567-0047Japan State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan430070China Graduate School of Engineering Osaka City University3-3-138 SugimotoOsaka558-8585Japan Department of Physical Science and Engineering Nagoya Institute of TechnologyNagoya 466-8555Japan

Biodegradable materials,with many advantages over conventionally used non-biodegradable materials,have received much attention owing to the elimination of the need for a secondary surgery for the removal of implants after *** with other biodegradable ceramics and/or polymers,Mg alloys are considered to be the most promising biodegradable orthopedic materials because they feature not only high specific strength and compressive yield strength but also a low Young’s modulus,which is comparable to that of human bones(10-30 GPa)[1,2].

关键词： strength aging alloys

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Tuning the Oxygen Vacancies and Mass Transfer of Porous Conductive Ceramic Supported Irox Catalyst Via Polyether Derived Composite Oxide Pyrolysis: Toward a Highly Efficient Oxygen Evolution Reaction Catalyst for Water Electrolysis

SSRN

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SSRN 2023年

作者： Zhang, Hao Zhu, Liyan Shen, Yuhan Wu, Mingjuan Tian, Tian 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 Hubei Key Laboratory of Fuel Cell Wuhan430070 China

Slow oxygen evolution reaction (OER) and material transport impedance in catalyst coated membrane (CCM) are major challenges for the practical proton exchange membrane water electrolyzer (PEMWE). Herein, we present a novel OER catalyst with a multilevel porous support and abundant oxygen vacancies to boost efficiency and durability in water electrolysis. The formation of a heterointerface with abundant oxygen vacancies in IrOx improves the catalytic activity and prevents IrOx from peroxidation. Furthermore, the unique pore structure of the support facilitates the mass transport of the anode catalyst layer during water electrolysis at high current density, and the material transport resistance of the water electrolyzer is only 0.0154 Ω cm2 at 1.5 A cm-2. When used in a PEMWE, the prepared electrocatalysts have an impressive electrochemical performance of 1.87 V at 3·A cm-2 with an Ir loading of only 0.91 mg cm-2. This approach highlights the importance of oxygen vacancies and transportation in the catalyst-support interface, providing a promising solution for high-rate practical water electrolysis. © 2023, The Authors. All rights reserved.

关键词： Mass transfer

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Boosting oxygen evolution of LiCoO2 electrocatalysts via lithium defect

Materials Today Catalysis

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Materials Today Catalysis 2025年 8卷

作者： Li, Huamei Li, Mengyuan Liao, Lingling Yang, Han Xiang, Kun Luo, Guoqiang Xie, Mingjiang School of Chemistry and Environmental Engineering Engineering Research Center of Phosphorus Resources Development and Utilization of Ministry of Education Wuhan Institute of Technology Wuhan430205 China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China Hubei Key Lab for Processing and Application of Catalytic Materials College of Chemical Engineering Huanggang Normal University Huanggang438000 China

The challenge of the complex oxygen evolution reaction (OER) currently impedes the efficient production of hydrogen via electrolytic water splitting. To address this issue, the development and improvement of effective electrocatalysts are required. LiCoO2, a key material in lithium-ion batteries, has shown promising potential as an electrocatalyst for electrochemical energy conversion. However, OER catalysts derived from LiCoO2 have faced obstacles such as high overpotential and a complicated preparation process. In this study, the preparation method is adjusted to optimize the synthesis of Li1-xCoO2 with a defective structure, resulting in an impressive overpotential of only 290 mV at a current density of 100 mA cm−2 and a remarkable Tafel slope of 15.2 mV dec−1. The exceptional catalytic activity of Li1-xCoO2 can be attributed to the absence of Li, which triggers oxidative alterations in the electronic structure of Co. Density functional theory (DFT) calculations reveal that Li defects can influence the d-band center of active Co sites, enhancing the adsorption capabilities of Co sites towards *OOH intermediates and increasing the conductivity of the electrocatalyst during the OER process. These alterations improve the velocity of the crucial step in the reaction, ultimately boosting the catalyst's overall performance and efficiency. © 2024 The Authors

关键词： Lithium-ion batteries

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Mn4+activated phosphors in photoelectric and energy conversion devices

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能源化学 2023年第11期86卷 277-299页

作者： Yang Ding Chunhua Wang Lang Pei Qinan Mao Sateesh Bandaru Runtian Zheng Soumyajit Maitra Meijiao Liu Li-Hua Chen Bao-Lian Su Jiasong Zhong College of Materials and Environmental Engineering Hangzhou Dianzi UniversityHangzhou 310018ZhejiangChina School of Energy and Environment City University of Hong KongKowloon 99077Hong KongChina Laboratory of Inorganic Materials Chemistry(CMI) University of Namur61 rue de Bruxelles B-5000NamurBelgium Department of Materials University of OxfordOxford OX1 3PHUK School of Chemistry and Chemical Engineering Zhejiang Sci-Tech UniversityHangzhou 310018ZhejiangChina State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070HubeiChina Laboratory of Inorganic Materials Chemistry(CMI) University of Namur61 rue de Bruxelles B-5000NamurBelgium State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070HubeiChina

Owing to their high luminous efficiency and tunable emission in both red light and far-red light regions,Mn4+ ion-activated phosphors have appealed significant interest in photoelectric and energy conversion devices such as white light emitting diode(W-LED),plant cultivation LED,and temperature *** to now,Mn4*has been widely introduced into the lattices of various inorganic hosts for brightly red-emitting ***,how to correlate the structure-activity relationship between host frame-work,luminescence property,and photoelectric device is urgently *** this review,we thor-oughly summarize the recent advances of Mn4+doped ***,several strategies like co-doping and defect passivation for improving Mn4+ emission are also *** importantly,the relationship between the protocols for tailoring the structures of Mn4+doped phosphors,increased luminescence performance,and the targeted devices with efficient photoelectric and energy conversion efficiency is deeply ***,the challenges and perspectives of Mn4+doped phosphors for prac-tical applications are *** cordially anticipate that this review can deliver a deep comprehen-sion of not only Mn4+luminescence mechanism but also the crystal structure tailoring strategy of phosphors,so as to spur innovative thoughts in designing advanced phosphors and deepening the applications.

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Surface-assembled highly flexible Na_(3)(VOPO_(4))_(2)F nanocube cathode for high-rate binder-free Na-ion batteries

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Chinese Chemical Letters 2021年第2期32卷 826-829页

作者： Bohua Deng Ning Yue Haoyang Dong Qiuyue Gui Liang Xiao Jinping Liu School of Chemistry Chemical Engineering and Life ScienceWuhan University of TechnologyWuhan 430070China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology.Wuhan 430070China Key Laboratory for Photonic and Electronic Bandgap Materials Ministry of EducationSchool of Physics and Electronic EngineeringHarbin Normal UniversityHarbin 150025China

Flexible Na-ion storage cathodes are still very few due to the challenge in achieving both reliable mechanical flexibility and excellent electrochemical ***,a new type of flexible Na_(3)(VOPO_(4))_(2)F cathode with nanocubes tightly assembled on carbon cloth is fabricated by a facile solvothe rmal method for the first *** cathode is able to exhibit superior rate capability and stable cycling performa nce up to 1000 cycles,due to the surface-assembling of crystalline nanocubes on carbon *** addition,it shows good mechanical flexibility,nearly no capacity decay is observed after continuous bending of 500 *** this novel cathode and a directly-grown Na_(2)Ti_(2)O_(5) anode,a fully binde r-free Na-ion battery is *** can deliver a high wo rking voltage and increased gravimetric energy/power densities(maximum values:220.2 Wh/kg;5674,7 W/kg),and can power a LED indicator at bending angles fro m 0° to 180°.

关键词： Flexible cathode Na_(3)(VOPO_(4))_(2)F Nanocube Surface-assembling Sodium-ion battery

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Directing Ni/Al Layered Double Hydroxides Nanosheets on Tubular Graphite Carbon Nitride for Promoted Photocatalytic Hydrogen Production

SSRN

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SSRN 2024年

作者： Jiang, Ze-Yu Ran, Mao-Jin Liu, Kai Huang, Yi-Fu Li, Zhi-Rong Shen, Ting-Ting Li, Wan-Ying Khojiev, Shokir Hu, Zhi-Yi Liu, Jing Chen, Li-Hua Li, Yu Su, Bao-Lian State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology 122 Luoshi Road Hubei Wuhan430070 China Wuhan University of Technology 122 Luoshi Road Hubei Wuhan430070 China Center for Advanced Technology under Agency for Innovative Development of the Republic of Uzbekistan The Ministry of Higher Education Science and Innovation University Street 3A Tashkent100174 Uzbekistan University of Namur 61 rue de Bruxelles NamurB-5000 Belgium State Key Laboratory of Advanced Technology for Materials Synthesis and Processing China

Constructing heterojunctions via in-situ growth or mechanical mixing have been widely used for improving the photogenerated carrier separation and photocatalytic activity. However, interface transfer impedance and the charge transfer channels of heterojunction prepared by in-situ method are rarely discussed. In this work, we use tubular g-C3N4 (TCN) as the basic photocatalyst and in-situ growth of nickel/aluminum layered double hydroxide (LDH) nanosheets as co-catalyst on the surface of TCN (TCN@Ni/Al-LDH) to show the advantage of the in-situ constructing heterojunction for highly enhanced photocatalytic hydrogen production. The results show that the TCN@Ni/Al-LDH-60 exhibits the best hydrogen production performance of 1428 μmol h-1 g-1, which is 53.3 and 21.33 times higher than that of TCN and mechanical prepared TCN/Ni/Al-LDH-60. For the first time, we propose a statistics model to reveal that the contact area of the heterojunction TCN@Ni/Al-LDH-60 is 2.88 times that of TCN/Ni/Al-LDH-60. This largely increases the charge transfer channels for the photogenerated carrier transport. In addition, the in-situ growth of TCN@Ni/Al-LDH composites increases the active sites, which improves the utilization efficiency of the photogenerated electrons. This study would shed some light on analyzing the in-situ constructing heterojunction photocatalysts for efficient photocatalytic hydrogen production through photocatalytic water splitting. © 2024, The Authors. All rights reserved.

关键词： Heterojunctions

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A Novel NASICON‑Type Na_(3.5)MnCr_(0.5)Ti_(0.5)(PO_(4))_(3)Nanofiber with Multi‑electron Reaction for High‑Performance Sodium‑Ion Batteries

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advanced Fiber Materials 2024年第2期6卷 561-569页

作者： Ting Zhu Wei Liu Xiaobin Liao Mengyao Wang Hao Fan Zihe Wei Congcong Cai Liyan Yang Mufang Li Dong Wang Ping Hu Xuanpeng Wang Key Laboratory of Textile Fiber and Products Ministry of EducationHubei International Scientific and Technological Cooperation Base of Intelligent TextileMaterials&ApplicationWuhan Textile UniversityWuhan 430200China Hubei Key Laboratory of Micro‑Nanoelectronic Materials and Devices School of MicroelectronicsHubei UniversityWuhan 430062China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Department of Physical Science&Technology School of ScienceWuhan University of TechnologyWuhan 430070China Hubei Longzhong Laboratory Wuhan University of Technology(Xiangyang Demonstration Zone)Xiangyang 441000China

Sodium superionic conductors(NASICONs)show significant promise for application in the development of cathodes for sodium-ion batteries(SIBs).However,it remains a major challenge to develop the desired multi-electron reaction cathode with a high specific capacity and energy ***,we report a novel NASICON-type Na_(3.5)MnCr_(0.5)Ti_(0.5)(PO_(4))_(3)cathode obtained by combining electrospinning and stepwise sintering *** cathode exhibits a high discharge capacity of 160.4 mAh g^(−1)and operates at a considerable medium voltage of 3.2 *** Na_(3.5)MnCr_(0.5)Ti_(0.5)(PO_(4))_(3)cathode undergoes a multi-electron redox reaction involving the Cr^(3+/4+)(4.40/4.31 V ***/Na^(+)),Mn^(3+/4+)(4.18/4.03 V),Mn^(2+/3+)(3.74/3.41 V),and Ti^(3+/4+)(2.04/2.14 V)redox *** redox reaction enables a three-electron transfer during the Na+intercalation/de-intercalation *** a result,the Na_(3.5)MnCr_(0.5)Ti_(0.5)(PO_(4))_(3)demonstrates a significant enhancement in energy density,surpassing other recently reported SIB *** highly reversible structure evolution and small volume changes during cycling were demonstrated with in-situ X-ray diffraction,ensuring outstanding cyclability with 77%capacity retention after 500 ***,a NMCTP@C//Sb@C full battery was fabricated,which delivered a high energy density of 421 Wh kg−1 and exhibited good cyclability with 75.7%capacity retention after 100 *** rational design of composition regulation with multi-metal ion substitution holds the potential to unlock new possibilities in achieving high-performance SIBs.

关键词： Sodium-ion battery NASICON structure Na_(3.5)MnCr_(0.5)Ti_(0.5)(PO_(4))_(3)nanofiber Ex/in-situ characterization Multi-electron reaction

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通过表面终止化学设计实现高度可逆的锌金属阳极

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Science Bulletin 2023年第23期68卷 2993-3002,M0005页

作者：刘宇陈树麟袁豪熊方宇刘琴安永康张建勇吴璐孙建国 Yong-Wei Zhang 安琴友 John Wang State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Department of Materials Science and Engineering National University of SingaporeSingapore 117574Singapore Institute of High Performance Computing Agency for ScienceTechnology and Research(A*Star)Singapore 138632Singapore Institute of Materials Research and Engineering(IMRE) Agency for ScienceTechnology and Research(A*Star)Singapore 138634Singapore

锌表面自然形成的非均匀氧化层(ZnO)会与电解液发生反应形成Zn_(4)(OH)_(6)SO_(4)·xH_(2)O(ZSH)副产物,导致锌负极表面非均匀沉积,从而阻碍水性锌离子电池实际应用.为了排除氧化层分布形式的影响,本文利用表面终止化学设计策略在... 详细信息

锌表面自然形成的非均匀氧化层(ZnO)会与电解液发生反应形成Zn_(4)(OH)_(6)SO_(4)·xH_(2)O(ZSH)副产物,导致锌负极表面非均匀沉积,从而阻碍水性锌离子电池实际应用.为了排除氧化层分布形式的影响,本文利用表面终止化学设计策略在锌负极表面制备了一层完全氧化的ZnO层,研究发现锌负极均匀分布的ZnO层会原位演化形成致密的ZSH功能层.均匀且致密的ZSH能够有效隔绝电解液的腐蚀,从而有效提高锌负极界面的稳定性.此外,ZSH(002)晶面边缘的不饱和悬空键(如-O)更容易和Zn(H_(2)O)_(6)^(2+)结构中的锌离子形成强Zn-O键,可以促进Zn(H_(2)O)_(6)^(2+)的脱溶剂化和锌离子沿边扩散,实现了高度可逆的锌沉积行为并限制了副反应.基于此,本文提出与“表面脱水-晶体通道转移”机制明显不同的“边缘脱水-沿边缘转移”锌离子输运新机制.更重要的是,基于此组装的全电池显示出高循环稳定性(超过1000次循环)和高库仑效率(99.07%),验证了其潜在的实际应用价值.

关键词： Zn-O termination Zn Anode Solid electrolyte interphase Dendrite-free Zn ion battery

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