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Layered niobium carbide enabling excellent kinetics and cycling stability of li-Mg-B-H hydrogen storage material Layered niobium carbide enabling excellent kinetics

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Rare Metals 2024年第3期43卷 1153-1166页

作者： li-Wen Lu Hui Luo Guang-Xu li Yun li Xin-Hua Wang Cun-Ke Huang Zhi-QiangLan Wen-Zheng Zhou Jin Guo Mohammad Ismail Hai-Zhen liu Guangxi Novel Battery Materials Research Center of Engineering Technology Guangxi Colleges and Universities Key Laboratory of Blue Energy and Systems IntegrationSchool of Physical Science and TechnologyGuangxi UniversityNanning530004China State Key Laboratory of Featured Metal Materials and life-Cycle Safety for Composite Structures Nanning530004China School of Mechanical and Electrical Engineering Quzhou College of TechnologyQuzhou324000China Department of Materials Science and Engineering Zhejiang UniversityHangzhou310027China Faculty of Ocean Engineering Technology and Informatics Universiti Malaysia Terengganu21030Kuala NerusTerengganuMalaysia Key Laboratory of Advanced Energy Materials Chemistry(Ministry of Education) Nankai UniversityTianjin300071China

The li-Mg-B-H composite(2liBH_(4)+MgH_(2))has a high capacity of 11.4 wt%as a hydrogen storage ***,the slow kinetics and poor cycling stability severely restrict its practical *** this work,a layered Nb_(2)C MXene was first synthesized and then introduced to tailor the kinetics and cycling stability of the li-Mg-B-H *** milled 2liH+MgB_(2)composites were initially hydrogenated to obtain the 2liBH_(4)+MgH_(2)*** 2liBH_(4)+MgH_(2)+5wt%Nb_(2)C can release 9.0 wt%H_(2)in 30 min at 400℃,while it is only 2.7 wt%for the undoped 2liBH_(4)+MgH_(2).The dehydrogenation activation energies of MgH_(2)and liBH_(4)are 123 and 154 kJ·mol^(-1)respectively for the 5 wt%Nb_(2)C-doped composite,lower than the undoped composite(164 and 165 kJ·mol^(-1)).The 2liBH_(4)+MgH_(2)+5 wt%Nb_(2)C possesses excellent cycling stability,with the reversible capacity only slightly reduced from 9.4 wt%for the 1st cycle to 9.3 wt%for the 20th ***_(2)C keeps stable in the composite and acts as an efficient catalyst for the li-Mg-B-H *** is believed that both the layered structure and the active Nb element contribu te to the enhanced hydrogen storage performances of the li-Mg-B-H *** work confirms that the Nb_(2)C MXene with layered stru cture has a significant enhancing impact on the li-Mg-B-H hydrogen storage materials,which is different from the bulk NbC.

关键词： Hydrogen storage lithium borohydride Magnesium hydride Nb_(2)C MXene

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Hard-carbon hybrid li-ion/metal anode enabled by preferred mesoporous uniform lithium growth mechanism

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Journal of Energy Chemistry 2024年第1期88卷 252-259,I0006页

作者： Fang Yan Yan liu Yuan li Yan Wang Zicen Deng Meng li Zhenwei Zhu Aohan Zhou Ting li Jingyi Qiu Gaoping Cao Shaobo Huang Biyan Wang Hao Zhang School of Chemistry and Biological Engineering University of Science and TechnologyBeijing 100083China Research Institute of Chemical Defense Beijing 100191China College of Physics and Engineering Henan University of Science and TechnologyLuoyang 471023HenanChina National Base for International Science&Technology Cooperation School of ChemistryXiangtan UniversityXiangtan 411105HunanChina Materials and Manufacturing Department Beijing University of TechnologyBeijing 100124China

To achieve high energy density in lithium batteries,the construction of lithium-ion/metal hybrid anodes is a promising *** particular,because of the anisotropy of graphite,hybrid anode formed by graphite/li metal has low transport kinetics and is easy to causes the growth of lithium dendrites and accumulation of dead li,which seriously affects the cycle life of batteries and even causes safety ***,by comparing graphite with two types of hard carbon,it was found that hybrid anode formed by hard carbon and lithium metal,possessing more disordered mesoporous structure and lithophilic groups,presents better *** indicate that the mesoporous structure provides abundant active site and storage space for dead *** the synergistic effect of this structure and lithophilic functional groups(–COOH),the reversibility of hard carbon/lithium metal hybrid anode is maintained,promoting uniform deposition of lithium metal and alleviating formation of lithium *** hybrid anode maintains a 99.5%Coulombic efficiency(CE)after 260 cycles at a specific capacity of 500 m Ah/*** work provides new insights into the hybrid anodes formed by carbon-based materials and lithium metal with high specific energy and fast charging ability.

关键词： Hard carbon/li metal hybrid anode Mesoporous structure Surface oxygen functional group Fast charging lithium batteries

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Enhanced electrochemical performance of li_(1.3)Al_(0.3)Ti_(1.7)(PO_(4))_(3) solid electrolyte by anion doping

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Nano Research 2024年第3期17卷 1465-1472页

作者： Jingrui Kang Xu Guo Rui Gu Honglei Hao Yi Tang Jiahui Wang li Jin Hongfei li Xiaoyong Wei Electronic Materials Research Laboratory Key Laboratory of the Ministry of Education&International Center for Dielectric ResearchSchool of Electronic and Information EngineeringXi’an Jiaotong UniversityXi’an 710049China School of Energy and Materials Shanghai Key Laboratory of Engineering Materials Application and EvaluationShanghai Polytechnic UniversityShanghai 201209China

Nowadays,the majority of the studies on the substitution are focused on cations(such as Y^(3+),Ti^(4+),P^(5+),etc.)in li_(1.3)Al_(0.3)Ti_(1.7)(PO_(4))_(3)(LATP),while there are few studies on the substitution of anion O^(2-).In this work,the modified LATP with a series of liCl(LATPClx,x=0.1,0.2,0.3,0.4)additives is prepared to enhance ionic *** successful introduction of Cl-makes the length of the c axis decrease from 20.822(2)to 20.792(1)Å,and the bulk conductivity of 2.13×10^(-3) S·cm^(-1) is achieved in LATPCl_(0.3).Moreover,the Al/Ti-O1/Cl1 and Al/Ti-O_(2)/Cl_(2) distance decrease,while the li1-O_(2)/Cl_(2) distance *** ions migrate more easily in the nanochannel of *** addition,the liCl additive increases the relative density and the grain boundary conductivity of LATPClx ***,a higher ionic conductivity of 2.12×10^(–4) S·cm^(-1) and a low activation energy of 0.30 eV are obtained in LATPCl_(0.3).Correspondingly,the symmetric cell exhibits a low overpotential of±50 mV for over 200 h in LATPCl_(0.3).The solid-state li|LATPCl_(0.3)|NCM811(NCM811=liNi0.8Co0.1Mn0.1O_(2))battery exhibits high initial capacity 185.1 mAh·g^(-1) with a capacity retention rate of 95.4%after 100 cycles at 0.5 *** result suggests that liCl additive is an effective strategy to promote electrochemical properties of LATP solid electrolyte and can be considered for reference to other inorganic solid electrolytes systems.

关键词： li_(1.3)Al_(0.3)Ti_(1.7)(PO_(4))_(3)(LATP)solid electrolyte anion doping ionic conductivity cyclic performance

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Catalytic anode surface enabling in situ polymerization of gel polymer electrolyte for stable li metal batteries

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Nano Research 2024年第6期17卷 5216-5223页

作者： Guocheng li Kang liang Yuanjian li Xiangrui Duan lin Fu Zhao Cai Zhaofu Zhang Jiangnan Dai Yongming Sun Wuhan National Laboratory for Optoelectronics Huazhong University of Science and TechnologyWuhan 430074China The Institute of Technological Sciences Wuhan UniversityWuhan 430074China Faculty of Materials Science and Chemistry China University of Geoscience(Wuhan)Wuhan 430074China

Employing quasi-solid-state gel polymer electrolyte(GPE)instead of the liquid counterpart has been regarded as a promising strategy for improving the electrochemical performance of li metal ***,the poor and uneven interfacial contact between li metal anode and GPE could cause large interfacial resistance and electrochemical li stripping/plating inhomogeneity,deteriorating the electrochemical ***,we proposed that the functional component of composite anode could work as the catalyst to promote the in situ polymerization reaction,and we experimentally realized the integration of polymerized-dioxolane electrolyte and li/li_(22)Sn_(5)/liF composite electrode with low interfacial resistance and good stability by in situ catalyzation ***,the reaction kinetics and stability of metallic li anode were significantly *** a demonstration,symmetric cell using such a GPE-li/li_(22)Sn_(5)/liF integration achieved stable cycling beyond 250 cycles with small potential hysteresis of 25 mV at 1 mA·cm^(−2)and 1 mAh·cm^(−2),far outperforming the counterpart regular GPE on pure *** with liNi0.5Co0.3Mn0.2O2,the full cell with the GPE-li/li_(22)Sn_(5)/liF integration maintained 85.7%of the original capacity after 100 cycles at 0.5 C(1 C=200 mA·g^(−1)).Our research provides a promising strategy for reducing the resistance between GPE and li metal anode,and realizes li metal batteries with enhance electrochemical performance.

关键词： catalyzation polymerization interface resistance interfacial stability li metal batteries electrochemical performance

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Vinyltrimethylsilane as a novel electrolyte additive for improving interfacial stability of li-rich cathode working in high voltage

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Chinese Chemical Letters 2024年第2期35卷 534-538页

作者： Bing Jiang Hao li Bi Luo Lehao liu lihua Chu Qiaobao Zhang Meicheng li State Key Laboratory of Alternate Electrical Power System with Renewable Energy Sources School of New EnergyNorth China Electric Power UniversityBeijing 102206China State Key Laboratory of Physical Chemistry of Solid Surfaces College of MaterialsXiamen UniversityXiamen 361005China

Boosting the interfacial stability between electrolyte and li-rich cathode material at high operating voltage is vital important to enhance the cycling stability of li-rich cathode materials for high-performance li-ion *** this work,vinyltrimethylsilane as a new type of organic silicon electrolyte additive is studied to address the interfacial instability of li-rich cathode material at high operating *** cells using vinyltrimethylsilane additive shows the high capacity retention of 73.9%after 300 cycles at 1 C,whereas the cells without this kind of additive only have the capacity retention of 58.9%.The improvement of stability is mainly attributed to the additive helping to form a more stable surface film for li-rich cathode material,thus avoiding direct contact between the electrolyte and the cathode material,slowing down the dissolution of metal ions and the decomposition of the electrolyte under high operating *** findings in this work shed some light on the design of stable cycling performance of li-rich cathode toward advanced li-ion batteries.

关键词： Vinyltrimethylsilane Electrolyte additive li-rich cathode Interfacial stability Capacity retention

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利用废弃聚酯面料降解产物制备水溶性聚酯的研究

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化工新型材料 2016年第12期44卷 229-231页

作者：鲁静李梦娟李思明葛明桥江南大学纺织服装学院无锡214122 生态纺织教育部重点实验室(江南大学) 无锡214122

采用乙二醇醇解法降解4种不同颜色的聚酯面料,得到4种不同颜色的晶体产物。对降解产物进行傅里叶红外光谱(FT-IR)、核磁共振氢谱(1 H-NMR)和示差扫描量热(DSC)等测试分析,发现不同颜色的降解产物分子结构相同,并证实了降解产物为对苯二... 详细信息

采用乙二醇醇解法降解4种不同颜色的聚酯面料,得到4种不同颜色的晶体产物。对降解产物进行傅里叶红外光谱(FT-IR)、核磁共振氢谱(1 H-NMR)和示差扫描量热(DSC)等测试分析,发现不同颜色的降解产物分子结构相同,并证实了降解产物为对苯二甲酸乙二醇酯(BHET)。将降解产物BHET作为主要原料,引入水溶性基团间苯二甲酸-5-磺酸钠(SIPA)与柔性基团二乙二醇(DEG),经由酯化、酯交换、熔融缩聚等反应,制备了水溶性聚酯(WSP)。分别改变SIPA及DEG的用量,发现随着SIPA及DEG用量的增加,WSP水溶性增强,DEG用量对WSP分子结构及玻璃化温度(Tg)并无明显影响。

关键词：废弃聚酯面料水溶性聚酯对苯二甲酸乙二醇酯水溶性

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Congener-derived template to construct lithiophilic organic-inorganic layer/interphase for high volumetric capacity dendrite-free li metal batteries

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Chinese Chemical Letters 2024年第3期35卷 453-460页

作者： Kang Yang Long li Yuanbin Xiao Qiaoli Zhang Chenpeng Xi Borong li Yan Yu Chengkai Yang Key Laboratory of Advanced Materials Technologies International(HongKong Macao and Taiwan)Joint Laboratory on Advanced Materials TechnologiesCollege of Materials Science and EngineeringFuzhou UniversityFuzhou 350108China

The development of lithium-metal batteries(LMBs)is seriously restricted by the out-of-control dendrites growth and infinite volume ***,a pervasive organic-inorganic layer construction strategy is reported for the composite lithium metal anode with congener-derived organic-inorganic solid electrolyte interphase(SEI).In this strategy,the organic-inorganic Ag@polydopamine(Ag@PDA)layer is coated on the arbitrary substrates by a simple two-step *** thin and stable congener-derived SEI is insitu formed with fewer inorganic components and more organic components during charging/*** polydopamine with sufficient adhesion groups and lithiophilic Ag layer realize near-zero nucleation overpotential during lithium *** low interface resistance and stable lithium deposition are ***,the practical areal and volumetric capacities of the composite anode with three-dimensional copper(3DCu)as the substrate are 10 mAh/cm^(2)and 1538 mAh/cm^3(*** mass of anode).The symmetrical cell shows very low polarization voltage(10 mV)and more than 2500 h cycles life at 1 mA/cm^(2)(1 mAh/cm^(2)).The liNi_(0.8)Co_(0.1)Mn_(0.1)O_(2)(NCM811)-based full cells show improved capacity retention(82%)after 100 cycles at 0.5 *** modified lithiophilic anode with congener-derived interphase provides a promising strategy to realize the next-generation dendrite-free LMBs.

关键词： lithium metal anode Congener-derived lithiophilicity Volumetric capacity Organic-inorganic interphase

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3D打印聚乳酸的改性研究与应用进展

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材料导报 2024年第8期38卷 252-261页

作者：郑思铭李蔚杨函瑞陈松魏取福江南大学纺织科学与工程学院江苏无锡214122 江苏苏丝丝绸股份有限公司江苏宿迁223800

聚乳酸(PLA)是一种生物可降解热塑性聚酯,是极有前景的生物基可降解材料之一。PLA具有优异的力学性能、良好的可塑性及生物相容性,是理想的3D打印材料。3D打印PLA材料在多个领域尤其是医用方面有巨大的潜力。然而,PLA固有的脆性和较差... 详细信息

聚乳酸(PLA)是一种生物可降解热塑性聚酯,是极有前景的生物基可降解材料之一。PLA具有优异的力学性能、良好的可塑性及生物相容性,是理想的3D打印材料。3D打印PLA材料在多个领域尤其是医用方面有巨大的潜力。然而,PLA固有的脆性和较差的耐热、耐水解性限制了它的应用范围。近年来,学者对3D打印PLA的改性进行了大量研究。本文归纳了3D打印PLA的研究进展,分别从共混改性、复合改性、立构复合、涂层法和化学改性这几方面讨论了提高材料性能的原理与方法,并对相关性能进行了分析对比。共混法虽然简单易操作,但不利于材料的均匀化,且有时改性效果不够明显。复合改性向PLA中加入碳基添加剂、金属添加剂、植物纤维等填料,改性同时可赋予3D打印PLA更多功能,但易出现界面不相容等问题。此外,还有立构复合、涂层法、化学改性等新方法具有重要的研究价值。在此基础上,结合目前3D打印PLA在实际应用中的发展情况,分析了3D打印PLA仍存在的问题,对3D打印PLA未来的研究方向进行了展望。

关键词：聚乳酸 3D打印力学性能热性能耐水解性

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Anion competition for li^(+)solvated coordination environments in poly(1,3 dioxolane)electrolyte to enable high-voltage lithium metal solid-state batteries

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Journal of Energy Chemistry 2024年第9期96卷 633-641页

作者： Qiujun Wang Yanqiang Ma Xiaomeng Jia Di Zhang Zhaojin li Huilan Sun Qujiang Sun Bo Wang li-Zhen Fan Hebei Key Laboratory of Flexible Functional Materials School of Materials Science and EngineeringHebei University of Science and TechnologyShijiazhuang 050000HebeiChina Beijing Advanced Innovation Center for Materials Genome Engineering Institute of Advanced Materials and TechnologyUniversity of Science and Technology BeijingBeijing 100083China

Gel-based polymer electrolytes are limited by the polarity of the residual solvent,which restricts the coupling-breaking behaviour during li^(+)conduction,resulting in the li^(+)transport kinetics being greatly ***,we designed anion competitive gel polymer electrolyte(ACPE)by introducing lithium difluoro(oxalato)borate(liDFOB)anion into the 1,3-dioxolane(DOL)in situ polymerisation *** enhances the ionic dipole interaction between li^(+)and the solvent molecules and synergizes with li^(+)across the solvation site of the polymer ethylene oxide(EO)unit,combination that greatly improves the li^(+)transport *** a result,ACPE exhibits 1.12 mS cm^(−1)ionic conductivity and 0.75 li^(+)transfer number at room ***,this intra-polymer solvation sheath allows preferential desolvation of DFOB−,which contributes to the formation of kinetically stable anion-derived interphase and effectively mitigates side *** results demonstrate that the assembled li||NCM622 solid-state battery exhibits lifespan of over 300 cycles with average Coulombic efficiency of 98.8%and capacity retention of 80.3%.This study introduces a novel approach for ion migration and interface design,paving the way for high-safety and high-energy-density batteries.

关键词： li-metal batteries Poly(1,3-dioxolane) In situ polymerization Solid-state polymer electrolytes Anion competition

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东北寒区水稻需水对地下水埋深的响应及灌溉模拟

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灌溉排水学报 2019年第12期38卷 68-77页

作者：田旖旎邵东国李思明王柏武汉大学水资源与水电工程科学国家重点实验室武汉430072 黑龙江省水利科学研究院哈尔滨100050

【目的】揭示不同降水年型下东北寒区水稻需水对地下水埋深变动与灌溉的响应规律,进一步优化寒区水稻灌溉制度。【方法】以黑龙江庆安和平灌区灌溉试验站多年水稻灌溉试验及2017年地下水动态观测数据为依据,分析不同灌水模式下水稻耗水... 详细信息

【目的】揭示不同降水年型下东北寒区水稻需水对地下水埋深变动与灌溉的响应规律,进一步优化寒区水稻灌溉制度。【方法】以黑龙江庆安和平灌区灌溉试验站多年水稻灌溉试验及2017年地下水动态观测数据为依据,分析不同灌水模式下水稻耗水及地下水变化动态,验证AquaCrop模型在东北寒区水稻生长模拟中的适用性,并用于模拟分析25%、50%、75%降水年型下水稻需水与不同地下水埋深的相互关系及灌水量的响应规律,提出适宜该地区水稻高产的地下水埋深范围及其生育期净灌水量。【结果】①水稻生育期内,地下水埋深先浅后深,其中,分蘖期、拔节孕穗期和抽穗开花期耗水量大,灌溉和降雨较多,地下水埋深较浅;②构建了3种降水年型下ET与GD、I的多元回归方程,综合考虑了水稻需水量与地下水埋深、生育期灌水量之间的相关关系,可用于稻田高效耗用水管理和地下水资源持续利用;③为实现东北寒区水稻高产和地下水埋深基本稳定的双重目标,地下水埋深应控制在2.0~2.5 m之间,水稻生育期净灌水量为:枯水年不宜低于现状灌水量,即300 mm;丰水年和平水年净灌水量可适当减少至现状灌水量的0.8倍,即240 mm。【结论】提出了适宜该地区水稻高产的地下水埋深范围及生育期净灌水量,为促进我国东北地区节水增粮,保护湿地生态环境,提高农业用水效率提供了理论依据。

关键词：寒区水稻需水地下水埋深灌水量 AquaCrop模型水分生产率

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