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Hard-carbon hybrid Li-ion/metal anode enabled by preferred mesoporous uniform lithium growth mechanism
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作者 Fang Yan Yan Liu +11 位作者 Yuan Li Yan Wang Zicen Deng Meng Li Zhenwei Zhu Aohan Zhou Ting Li Jingyi Qiu Gaoping Cao Shaobo Huang Biyan Wang Hao Zhang 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2024年第1期252-259,I0006,共9页
To achieve high energy density in lithium batteries,the construction of lithium-ion/metal hybrid anodes is a promising strategy.In particular,because of the anisotropy of graphite,hybrid anode formed by graphite/Li me... To achieve high energy density in lithium batteries,the construction of lithium-ion/metal hybrid anodes is a promising strategy.In 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 problems.Here,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 performance.Results indicate that the mesoporous structure provides abundant active site and storage space for dead lithium.With 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 dendrites.The hybrid anode maintains a 99.5%Coulombic efficiency(CE)after 260 cycles at a specific capacity of 500 m Ah/g.This work provides new insights into the hybrid anodes formed by carbon-based materials and lithium metal with high specific energy and fast charging ability. 展开更多
关键词 Hard carbon/li metal hybrid anode Mesoporous structure Surface oxygen functional group Fast charging lithium batteries
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From Liquid to Solid‑State Lithium Metal Batteries:Fundamental Issues and Recent Developments
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作者 Zhao Zhang Wei‑Qiang Han 《Nano-Micro Letters》 SCIE EI CAS CSCD 2024年第2期68-125,共58页
The widespread adoption of lithium-ion batteries has been driven by the proliferation of portable electronic devices and electric vehicles,which have increasingly stringent energy density requirements.Lithium metal ba... The widespread adoption of lithium-ion batteries has been driven by the proliferation of portable electronic devices and electric vehicles,which have increasingly stringent energy density requirements.Lithium metal batteries(LMBs),with their ultralow reduction potential and high theoretical capacity,are widely regarded as the most promising technical pathway for achieving high energy density batteries.In this review,we provide a comprehensive overview of fundamental issues related to high reactivity and migrated interfaces in LMBs.Furthermore,we propose improved strategies involving interface engineering,3D current collector design,electrolyte optimization,separator modification,application of alloyed anodes,and external field regulation to address these challenges.The utilization of solid-state electrolytes can significantly enhance the safety of LMBs and represents the only viable approach for advancing them.This review also encompasses the variation in fundamental issues and design strategies for the transition from liquid to solid electrolytes.Particularly noteworthy is that the introduction of SSEs will exacerbate differences in electrochemical and mechanical properties at the interface,leading to increased interface inhomogeneity—a critical factor contributing to failure in all-solidstate lithium metal batteries.Based on recent research works,this perspective highlights the current status of research on developing high-performance LMBs. 展开更多
关键词 lithium metal batteries All-solid-state lithium metal battery li dendrite Solid electrolyte Interface
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Accurate estimation of Li/Ni mixing degree of lithium nickel oxide cathode materials
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作者 陈鹏浩 徐磊 +1 位作者 禹习谦 李泓 《Chinese Physics B》 SCIE EI CAS CSCD 2024年第5期631-635,共5页
Li/Ni mixing negatively influences the discharge capacity of lithium nickel oxide and high-nickel ternary cathode materials.However,accurately measuring the Li/Ni mixing degree is difficult due to the preferred orient... Li/Ni mixing negatively influences the discharge capacity of lithium nickel oxide and high-nickel ternary cathode materials.However,accurately measuring the Li/Ni mixing degree is difficult due to the preferred orientation of labbased XRD measurements using Bragg–Brentano geometry.Here,we find that employing spherical harmonics in Rietveld refinement to eliminate the preferred orientation can significantly decrease the measurement error of the Li/Ni mixing ratio.The Li/Ni mixing ratio obtained from Rietveld refinement with spherical harmonics shows a strong correlation with discharge capacity,which means the electrochemical capacity of lithium nickel oxide and high-nickel ternary cathode can be estimated by the Li/Ni mixing degree.Our findings provide a simple and accurate method to estimate the Li/Ni mixing degree,which is valuable to the structural analysis and screening of the synthesis conditions of lithium nickel oxide and high-nickel ternary cathode materials. 展开更多
关键词 lithium nickel oxide high-nickel ternary cathode li/Ni mixing spherical harmonics function discharge capacity
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Thin polymer electrolyte with MXene functional layer for uniform Li^(+) deposition in all-solid-state lithium battery
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作者 Weijie Kou Yafang Zhang +3 位作者 Wenjia Wu Zibiao Guo Quanxian Hua Jingtao Wang 《Green Energy & Environment》 SCIE EI CAS CSCD 2024年第1期71-80,共10页
Solid polymer electrolyte(SPE) shows great potential for all-solid-state batteries because of the inherent safety and flexibility;however, the unfavourable Li+deposition and large thickness hamper its development and ... Solid polymer electrolyte(SPE) shows great potential for all-solid-state batteries because of the inherent safety and flexibility;however, the unfavourable Li+deposition and large thickness hamper its development and application. Herein, a laminar MXene functional layer-thin SPE layer-cathode integration(MXene-PEO-LFP) is designed and fabricated. The MXene functional layer formed by stacking rigid MXene nanosheets imparts higher compressive strength relative to PEO electrolyte layer. And the abundant negatively-charged groups on MXene functional layer effectively repel anions and attract cations to adjust the charge distribution behavior at electrolyte–anode interface. Furthermore,the functional layer with rich lithiophilic groups and outstanding electronic conductivity results in low Li nucleation overpotential and nucleation energy barrier. In consequence, the cell assembled with MXene-PEO-LFP, where the PEO electrolyte layer is only 12 μm, much thinner than most solid electrolytes, exhibits uniform, dendrite-free Li+deposition and excellent cycling stability. High capacity(142.8 mAh g-1), stable operation of 140 cycles(capacity decay per cycle, 0.065%), and low polarization potential(0.5 C) are obtained in this Li|MXene-PEO-LFP cell,which is superior to most PEO-based electrolytes under identical condition. This integrated design may provide a strategy for the large-scale application of thin polymer electrolytes in all-solid-state battery. 展开更多
关键词 MXene nanosheet Laminar functional layer Thin polymer electrolyte Dendrite-free liþdeposition All-solid-state lithium battery
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A layered multifunctional framework based on polyacrylonitrile and MOF derivatives for stable lithium metal anode
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作者 Fanfan Liu Peng Zuo +5 位作者 Jing Li Pengcheng Shi Yu Shao Linwei Chen Yihong Tan Tao Ma 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2024年第6期282-288,I0007,共8页
Composite Li metal anodes based on three-dimensional(3D) porous frameworks have been considered as an effective material for achieving stable Li metal batteries with high energy density.However,uneven Li deposition be... Composite Li metal anodes based on three-dimensional(3D) porous frameworks have been considered as an effective material for achieving stable Li metal batteries with high energy density.However,uneven Li deposition behavior still occurs at the top of 3D frameworks owing to the local accumulation of Li ions.To promote uniform Li deposition without top dendrite growth,herein,a layered multifunctional framework based on oxidation-treated polyacrylonitrile(OPAN) and metal-organic framework(MOF) derivatives was proposed for rationally regulating the distribution of Li ions flux,nucleation sites,and electrical conductivity.Profiting from these merits,the OPAN/carbon nano fiber-MOF(CMOF) composite framework demonstrated a reversible Li plating/stripping behavior for 500 cycles with a stable Coulombic efficiency of around 99.0% at the current density of 2 mA/cm~2.Besides,such a Li composite anode exhibited a superior cycle lifespan of over 1300 h under a low polarized voltage of 18 mV in symmetrical cells.When the Li composite anode was paired with LiFePO_(4)(LFP) cathode,the obtained full cell exhibited a stable cycling over 500 cycles.Moreover,the COMSOL Multiphysics simulation was conducted to reveal the effects on homogeneous Li ions distribution derived from the above-mentioned OPAN/CMOF framework and electrical insulation/conduction design.These electrochemical and simulated results shed light on the difficulties of designing stable and safe Li metal anode via optimizing the 3D frameworks. 展开更多
关键词 lithium metal anode Layered multifunctional framework Ions flux redistribution Electrical insulation/conduction structure Uniform li deposition
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Postmortem ^(7)Li NMR analysis for assessing the reversibility of lithium metal electrodes in lithium metal batteries
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作者 Jaewon Baek Sunha Kim +1 位作者 Hee-Tak Kim Oc Hee Han 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2024年第7期430-440,共11页
Despite the proficiency of lithium(Li)-7 NMR spectroscopy in delineating the physical and chemical states of Li metal electrodes,challenges in specimen preparation and interpretation impede its progress.In this study,... Despite the proficiency of lithium(Li)-7 NMR spectroscopy in delineating the physical and chemical states of Li metal electrodes,challenges in specimen preparation and interpretation impede its progress.In this study,we conducted a comprehensive postmortem analysis utilizing ^(7)Li NMR,employing a stan-dard magic angle spinning probe to examine protective-layer coated Li metal electrodes and LiAg alloy electrodes against bare Li metal electrodes within Li metal batteries(LMBs).Our investigation explores the effects of sample burrs,alignment with the magnetic field,the existence of liquid electrolytes,and precycling on the ^(7)Li NMR signals.Through contrasting NMR spectra before and after cycling,we identi-fied alterations in Li^(0) and Li^(+) signals attributable to the degradation of the Li metal electrode.Our NMR analyses decisively demonstrate the efficacy of the protective layer in mitigating dendrite and solid elec-trolyte interphase formation.Moreover,we noted that Li*ions near the Li metal surface exhibit magnetic susceptibility anisotropy,revealing a novel approach to studying diamagnetic species on Li metal elec-trodes in LMBs.This study provides valuable insights and practical guidelines for characterizing distinct lithium states within LMBs. 展开更多
关键词 NMR spectroscopy lithium-7 lithium metal battery Electrolyte Electrode-protective layer Solid electrolyte interface Magnetic susceptibility anisotropy lithium-metal NMR signal Diamagnetic^(7)li NMR signal
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All-Solid-State Thin-Film Lithium-Sulfur Batteries 被引量:3
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作者 Renming Deng Bingyuan Ke +5 位作者 Yonghui Xie Shoulin Cheng Congcong Zhang Hong Zhang Bingan Lu Xinghui Wang 《Nano-Micro Letters》 SCIE EI CAS CSCD 2023年第5期326-338,共13页
Lithium-sulfur(Li-S)system coupled with thin-film solid electrolyte as a novel high-energy micro-battery has enormous potential for complementing embedded energy harvesters to enable the autonomy of the Internet of Th... Lithium-sulfur(Li-S)system coupled with thin-film solid electrolyte as a novel high-energy micro-battery has enormous potential for complementing embedded energy harvesters to enable the autonomy of the Internet of Things microdevice.However,the volatility in high vacuum and intrinsic sluggish kinetics of S hinder researchers from empirically integrating it into allsolid-state thin-film batteries,leading to inexperience in fabricating all-solid-state thin-film Li-S batteries(TFLSBs).Herein,for the first time,TFLSBs have been successfully constructed by stacking vertical graphene nanosheets-Li2S(VGsLi2S)composite thin-film cathode,lithium-phosphorous-oxynitride(LiPON)thin-film solid electrolyte,and Li metal anode.Fundamentally eliminating Lipolysulfide shuttle effect and maintaining a stable VGs-Li2S/LiPON interface upon prolonged cycles have been well identified by employing the solid-state Li-S system with an“unlimited Li”reservoir,which exhibits excellent longterm cycling stability with a capacity retention of 81%for 3,000 cycles,and an exceptional high temperature tolerance up to 60℃.More impressively,VGs-Li2S-based TFLSBs with evaporated-Li thin-film anode also demonstrate outstanding cycling performance over 500 cycles with a high Coulombic efficiency of 99.71%.Collectively,this study presents a new development strategy for secure and high-performance rechargeable all-solid-state thin-film batteries. 展开更多
关键词 All-solid-state thin-film batteries li-S batteries Vertical graphene nanosheets lithium phosphorous oxynitride li2S
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Nano silica aerogel-induced formation of an organic/alloy biphasic interfacial layer enables construction of stable high-energy lithium metal batteries 被引量:1
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作者 Chengwei Ma Xinyu Zhang +6 位作者 Chengcai Liu Yuanxing Zhang Yuanshen Wang Ling Liu Zhikun Zhao Borong Wu Daobin Mu 《Green Energy & Environment》 SCIE EI CAS CSCD 2023年第4期1071-1080,共10页
Lithium metal batteries represent promising candidates for high-energy-density batteries, however, many challenges must still be overcome,e.g., interface instability and dendrite growth. In this work, nano silica aero... Lithium metal batteries represent promising candidates for high-energy-density batteries, however, many challenges must still be overcome,e.g., interface instability and dendrite growth. In this work, nano silica aerogel was employed to generate a hybrid film with high lithium ion conductivity(0.6 mS cm^(-1)at room temperature) via an in situ crosslinking reaction. TOF-SIMS profile analysis has revealed conversion mechanism of hybrid film to Li–Si alloy/Li F biphasic interface layer, suggesting that the Li–Si alloy and Li F-rich interface layer promoted rapid Li+transport and shielded the Li anodes from corrosive reactions with electrolyte-derived products. When coupled with nickel-cobalt-manganese-based cathodes, the batteries achieve outstanding capacity retention over 1000 cycles at 1 C. Additionally the developed film coated on Li enabled high coulombic efficiency(99.5%) after long-term cycling when coupled with S cathodes. Overall, the results presented herein confirm an effective strategy for the development of high-energy batteries. 展开更多
关键词 lithium metal batteries Nano silica aerogel In situ crosslinking Biphasic interface layer li–Si alloy
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Performance comparison of lithium fractionation from magnesium via continuous selective nanofiltration/electrodialysis
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作者 Yong Xu Qingbai Chen +3 位作者 Yang Gao Jianyou Wang Huiqing Fan Fei Zhao 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2023年第7期42-50,共9页
Although selective nanofiltration(SNF)and selective electrodialysis(SED)have been widely adopted in the field of Mg^(2+)/Li^(+)separation,their differences have not been illustrated systematically.In this study,for th... Although selective nanofiltration(SNF)and selective electrodialysis(SED)have been widely adopted in the field of Mg^(2+)/Li^(+)separation,their differences have not been illustrated systematically.In this study,for the first time,SNF and SED processes in continuous mode were studied for Li+fractionation from the same brine with high Mg/Li ratios and their differences were discussed in detail.For a fair analysis of the two processes,typical factors were optimized.Specifically,the optimal operating pressure and feed flow rate for SNF were 2.4 MPa and 140 L·h^(-1),respectively,while the optimal cell-pair voltage and replenishment flow rate for SED were 1.0 V and 14 L·h^(-1),respectively.Although the Li^(+)fractionation capacity of the two processes were similar,the selectivity coefficient of SNF was 24.7% higher than that of SED and,thus,the Mg/Li ratio in purified stream of the former was 19.0% lower than that of the latter.Due to higher ion driving force,SED had clear advantages in recovery ratio and concentration effects.Meanwhile,the specific energy consumption of SED was 20.1% lower than that of SNF.This study provided a better understanding and guidance for the application and improvement of the two technologies. 展开更多
关键词 High Mg/li brine PURIFICATION Membrane NANOFILTRATION ELECTRODIALYSIS lithium recovery
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LiODFP在锂离子电池正极氧化分解的DFT研究
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作者 王雅婷 林钰涵 +1 位作者 刘军 施志聪 《电池》 CAS 北大核心 2024年第1期35-40,共6页
使用密度泛函理论(DFT),研究锂盐二氟二草酸磷酸锂(LiODFP)作为成膜添加剂在锂离子电池正极的作用机理。各研究体系的氧化电势理论计算值的排列顺序为:碳酸酯(包括EC、PC、EMC和DMC)>ODFP^(-)(单分子)≈碳酸酯-ODFP^(-)配合物。ODFP^... 使用密度泛函理论(DFT),研究锂盐二氟二草酸磷酸锂(LiODFP)作为成膜添加剂在锂离子电池正极的作用机理。各研究体系的氧化电势理论计算值的排列顺序为:碳酸酯(包括EC、PC、EMC和DMC)>ODFP^(-)(单分子)≈碳酸酯-ODFP^(-)配合物。ODFP^(-)优先于碳酸酯发生氧化反应,ODFP^(-)结构分解的路径比EC分子分解的路径更容易进行。EC+ODFP^(-)-e体系可能发生的分解反应路径是ODFP^(-)结构开环,生成CO、CO_(2)和自由基R1。R1可能进一步发生自由基终止反应,生成含有氟代磷酸盐单体的低聚物,从而抑制碳酸酯溶剂分子的氧化分解。 展开更多
关键词 锂离子电池 电解液 氧化分解 新型锂盐 密度泛函理论(DFT)
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Li^(+)浓度对化学增强锂铝硅玻璃性能的影响
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作者 田昊东 徐驰 +2 位作者 胥爽 李现梓 祖成奎 《材料导报》 EI CAS CSCD 北大核心 2024年第S01期137-142,共6页
采用一步法化学增强工艺,研究了熔盐中Li^(+)的富集对不同厚度锂铝硅玻璃表面压应力、应力层深度、弯曲强度、硬度等性能的影响,选择Na_(3)PO_(4)作为熔盐除杂剂并对净化效果进行了评定。研究表明:熔盐中Li^(+)浓度增加至4800×10^(... 采用一步法化学增强工艺,研究了熔盐中Li^(+)的富集对不同厚度锂铝硅玻璃表面压应力、应力层深度、弯曲强度、硬度等性能的影响,选择Na_(3)PO_(4)作为熔盐除杂剂并对净化效果进行了评定。研究表明:熔盐中Li^(+)浓度增加至4800×10^(-6),3 mm化学增强锂铝硅玻璃的表面压应力、弯曲强度、硬度下降16.8%、16.8%、10.6%;8 mm化学增强锂铝硅玻璃的表面压应力、弯曲强度、硬度下降17.6%、14.7%、9.8%。熔盐中Li^(+)浓度的变化未对化学增强锂铝硅玻璃应力层深度产生明显影响。Na_(3)PO_(4)具有较好的除杂效果,化学增强锂铝硅玻璃的表面压应力、弯曲强度、硬度得到了明显的恢复,为保证化学增强锂铝硅玻璃在可见光波段具有较高的透光率,除杂剂Na_(3)PO_(4)的掺量不宜超过1%(质量分数)。 展开更多
关键词 锂铝硅玻璃 化学增强 离子交换 li^(+)浓度 熔盐净化 半无限扩散模型
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Li_(7)La_(3)Zr_(2)O_(12)固态电解质负极界面研究进展
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作者 吴非 刘涛 《材料科学与工程学报》 CAS CSCD 北大核心 2024年第2期311-319,共9页
石榴石型固态电解质锂镧锆氧(Li_(7)La_(3)Zr_(2)O_(12),LLZO)具有高达5 V的宽电化学窗口,在固态电解质体系中,与金属锂负极具有良好的匹配性,使其有望成为下一代高能量电池。但LLZO与电极界面的稳定性问题极大地限制了其实际应用。本... 石榴石型固态电解质锂镧锆氧(Li_(7)La_(3)Zr_(2)O_(12),LLZO)具有高达5 V的宽电化学窗口,在固态电解质体系中,与金属锂负极具有良好的匹配性,使其有望成为下一代高能量电池。但LLZO与电极界面的稳定性问题极大地限制了其实际应用。本文从金属锂负极特性、LLZO电解质特性、LLZO/Li界面接触三个方面对LLZO/Li界面的稳定性问题展开分析,阐述界面稳定性的根源,同时对界面优化方法进行总结,提出LLZO/Li负极界面发展应注意的问题。 展开更多
关键词 LLZO负极界面改性 金属锂负极 全固态锂电池 LLZO/li界面微观机理
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Mg^(2+)掺杂对富锂层状氧化物材料Li_(1.2)Mn_(0.54)Ni_(0.13)Co_(0.13)O_(2)的影响
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作者 解自奇 谭玉婷 +2 位作者 赵妮 周明东 颜文超 《辽宁石油化工大学学报》 CAS 2024年第2期22-28,共7页
Mg^(2+)作为一种电化学惰性的阳离子,由于其离子半径(0.072 nm)与Li^(+)的离子半径(0.076 nm)相近,因此被广泛应用于取代富锂层状氧化物(LLOs)材料中Li^(+)的位置。然而,Mg^(2+)对LLOs材料晶体结构的影响还存在争议。利用溶胶凝胶法成... Mg^(2+)作为一种电化学惰性的阳离子,由于其离子半径(0.072 nm)与Li^(+)的离子半径(0.076 nm)相近,因此被广泛应用于取代富锂层状氧化物(LLOs)材料中Li^(+)的位置。然而,Mg^(2+)对LLOs材料晶体结构的影响还存在争议。利用溶胶凝胶法成功制备了一系列Mg^(2+)掺杂富锂正极材料Li_(1.2-x)Mg_(x)Mn_(0.54)Ni_(0.13)Co_(0.13)O_(2),通过X射线衍射仪和X射线光电子能谱等对其晶体结构和元素价态进行了系统的研究。结果表明,Mg^(2+)掺杂导致LLOs材料晶胞参数的增加。通过与Li_(1.2)Mn_(0.54)Ni_(0.13)Co_(0.13)O_(2)材料的电化学性能对比发现,Mg^(2+)掺杂有效地提高了LLOs材料的电化学性能。经过优化后,Mg-0.03样品展现出最优异的电化学性能,在0.1 C倍率下的初始放电比容量为291.9 mA•h/g,首圈库伦效率为78.40%。 展开更多
关键词 锂离子电池 富锂层状氧化物 正极材料 溶胶凝胶法 Mg^(2+)掺杂
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无钴富锂锰基正极材料Li_(1.2)Ni_(0.2)Mn_(0.6)O_(2)的表面改性及电化学性能研究
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作者 朱守聪 施志聪 《材料研究与应用》 CAS 2024年第2期241-247,共7页
无钴富锂锰基正极材料Li_(1.2)Ni_(0.2)Mn_(0.6)O_(2)因高比容量、低成本等优点备受关注,是极具潜力的下一代锂离子电池正极材料。然而,Li_(1.2)Ni_(0.2)Mn_(0.6)O_(2)材料存在首次库伦效率低、倍率性能差及容量衰减等问题,限制了其进... 无钴富锂锰基正极材料Li_(1.2)Ni_(0.2)Mn_(0.6)O_(2)因高比容量、低成本等优点备受关注,是极具潜力的下一代锂离子电池正极材料。然而,Li_(1.2)Ni_(0.2)Mn_(0.6)O_(2)材料存在首次库伦效率低、倍率性能差及容量衰减等问题,限制了其进一步发展。为解决此问题,采用柠檬酸溶液表面处理结合再重新煅烧方法,通过在其表面包覆一层尖晶石相,对Li_(1.2)Ni_(0.2)Mn_(0.6)O_(2)开展了表面改性研究,并对改性前后样品进行物理表征和电化学测试分析。结果表明,改性前后的Li_(1.2)Ni_(0.2)Mn_(0.6)O_(2)正极材料,形貌基本一致,均为尺寸100—400 nm的不规则颗粒,改性后的粉末颗粒边缘略有不平整。使用柠檬酸溶液表面处理后,Li_(1.2)Ni_(0.2)Mn_(0.6)O_(2)材料形成了内部为层状相、表面为尖晶石相的结构。尖晶石相的存在不仅为锂离子扩散提供了三维离子扩散通道、提高倍率性能,还可充当正极材料表面与电解液间的保护层,提高首次库伦效率,改善循环性能。改性后的Li_(1.2)Ni_(0.2)Mn_(0.6)O_(2)的首次库伦效率为92.4%,可逆比容量为292 mAh·g^(-1),与改性前相比分别提高了13.8%和22 mAh·g^(-1),并且在不同倍率下的可逆比容量和长循环容量保持率均有明显提升,表明其具有更好的倍率性能和更优的循环稳定性能。本研究提出了一种无钴富锂锰基正极材料表面改性方法,该改性方法操作简单、效果明显,可应用于不同组分的富锂正极材料,为富锂锰基正极材料的进一步发展提供了新的思路。 展开更多
关键词 锂离子电池 富锂正极材料 富锂锰基正极材料 表面改性 首次库伦效率 尖晶石相 电化学性能 可逆比容量
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液-固相法合成LiMn_(0.6)Fe_(0.4)PO_(4)的性能
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作者 李亨利 徐荣益 +1 位作者 王昭沛 李意能 《电池》 CAS 北大核心 2024年第2期205-208,共4页
磷酸锰锂(LiMnPO_(4))材料的电导率低且充放电过程易发生Jahn-Teller效应,导致电化学性能不理想。通过液-固相法合成磷酸锰铁锂(LiMn_(0.6)Fe_(0.4)PO_(4))正极材料,并对晶体结构、放电曲线特性、循环性能等进行分析。Fe均匀地掺入Mn位... 磷酸锰锂(LiMnPO_(4))材料的电导率低且充放电过程易发生Jahn-Teller效应,导致电化学性能不理想。通过液-固相法合成磷酸锰铁锂(LiMn_(0.6)Fe_(0.4)PO_(4))正极材料,并对晶体结构、放电曲线特性、循环性能等进行分析。Fe均匀地掺入Mn位形成固溶体,样品的常温电化学性能得到改善。在2.0~4.3 V循环,0.1 C倍率下的放电比容量为156.5 mAh/g;以1.0 C倍率循环2000次,容量保持率超过80%。容量衰减主要源于循环过程中正极材料颗粒产生裂纹及颗粒粉化。 展开更多
关键词 锂离子电池 正极材料 磷酸锰铁锂(liMn_(0.6)Fe_(0.4)PO_(4)) 容量衰减 掺杂 液-固相法 固溶体
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川西甲基卡伟晶岩型锂矿科学钻探(JSD-1)岩芯Li-B-Fe-Nd同位素对稀有金属成矿作用的指示意义 被引量:2
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作者 魏海珍 李伟强 +6 位作者 高建国 魏广祎 罗祥龙 环淳 左达昇 朱文斌 许志琴 《地质学报》 EI CAS CSCD 北大核心 2023年第10期3147-3167,共21页
甲基卡伟晶岩型锂矿位于青藏高原东部松潘-甘孜地体东南部,是我国最大的硬岩型锂矿,其成岩成矿机制至今仍有争议。为了深入认识甲基卡伟晶岩型锂矿床稀有金属超常富集的关键岩浆热液过程,研究团队基于甲基卡一号钻孔(JSD-1)岩芯开展全孔... 甲基卡伟晶岩型锂矿位于青藏高原东部松潘-甘孜地体东南部,是我国最大的硬岩型锂矿,其成岩成矿机制至今仍有争议。为了深入认识甲基卡伟晶岩型锂矿床稀有金属超常富集的关键岩浆热液过程,研究团队基于甲基卡一号钻孔(JSD-1)岩芯开展全孔Li-B-Fe-Nd同位素地球化学研究。伟晶岩和二云母花岗岩较低的Nb/Ta、Zr/Hf值以及Li-Nd同位素表明甲基卡伟晶岩可能来源于马颈子二云母花岗岩深成岩体的岩浆结晶分异。JSD-1岩芯花岗岩和伟晶岩中电气石的硼同位素(δ^(11)B)在-9.5‰~-7.1‰之间,与世界上90%的花岗岩和伟晶岩中δ^(11)B变化范围一致。JSD-1岩芯电气石δ^(11)B与全岩Li含量的实验和模型模拟结果表明花岗质岩浆演化过程遵循平衡结晶模型,花岗质岩浆极端结晶分异不能达到熔体中锂辉石过饱和。JSD-1岩芯全岩的Fe同位素(δ^(56)Fe)变化范围为-0.12‰~0.38‰。δ^(56)Fe的显著变化反映了黑云母分离结晶、热液蚀变(电气石化)以及石榴子石堆晶等多阶段岩浆-热液过程的共同结果。全孔Li-B-Fe-Nd同位素综合表明,伴随着广泛流体出溶的岩浆结晶分异过程控制了Li的逐步富集。由于岩浆上升的减压作用,花岗岩岩席穹隆的形成有利于晚期花岗岩岩浆的大量流体出溶,使得浅部形成锂辉石为主的矿体。 展开更多
关键词 伟晶岩锂矿 科学钻探 li-Nd-B-Fe同位素 成矿作用
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黔西南普安青山一带锂(Li)异常特征及找矿意义
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作者 方永坤 余杰 +3 位作者 刘文军 黄廷文 叶琼 陈智 《贵州地质》 2023年第3期216-223,共8页
根据《锂(Li)地球化学图》(贵州省地球化学图集,冯济舟等,2008)显示,晴隆县城北侧一带、普安青山一带、兴义万屯一带、安龙县城北侧一带均有较好的锂(Li)异常显示。经研究选取了普安青山一带开展了少量地质工作,发现锂(Li)异常层位主要... 根据《锂(Li)地球化学图》(贵州省地球化学图集,冯济舟等,2008)显示,晴隆县城北侧一带、普安青山一带、兴义万屯一带、安龙县城北侧一带均有较好的锂(Li)异常显示。经研究选取了普安青山一带开展了少量地质工作,发现锂(Li)异常层位主要为第四系(Q)残坡积松散黏土层,含锂(Li)黏土基底为强风化白云岩,下部为杂色黏土夹少量强风化白云岩碎块,中下部为土黄色、浅紫色黏土,中部及上部为褐红色黏土。经地表及浅井工程采集样品检测,基底白云岩含锂(Li)14.4 ug/g,黏土中锂(Li)含量最高达303 ug/g,平均含量200 ug/g,超过锂(Li)元素在地壳中克拉克值的10倍。经初步分析,本次研究工作显示了黔西南锂(Li)异常区具备一定的研究价值和找矿潜力。 展开更多
关键词 锂(li)异常特征 找矿潜力 普安青山 黔西南
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Three dimensional porous frameworks for lithium dendrite suppression 被引量:15
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作者 Shuyan Ni Shuangshuang Tan +1 位作者 Qinyou An Liqiang Mai 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2020年第5期73-89,共17页
Lithium metal is a promising anode material owing to its very low electrochemical potential and ultrahigh specific capacity.However,the growth of lithium dendrites could result in a short lifespan,low coulombic effici... Lithium metal is a promising anode material owing to its very low electrochemical potential and ultrahigh specific capacity.However,the growth of lithium dendrites could result in a short lifespan,low coulombic efficiency,and potential safety hazards during the progress of lithium plating/stripping.These factors drastically hinder its application in lithium metal batteries.This review focuses on the use of three dimensional(3D)porous host frameworks to improve Li plating/stripping behaviors,accommodate the change in volume,and suppress or block lithium dendrite growth.Various 3D porous frameworks,including the conductive carbon-based,metal-based,and lithiophilic inorganic-compound frameworks are introduced and summarized in detail.The particular functions,relative developments,and optimized strategies of various 3D porous frameworks for lithium deposition/dissolution behaviors are discussed.Moreover,the challenges and promising developments in the field of Li metal anodes will be discussed at the end of this review. 展开更多
关键词 lithium metal battery 3D porous frameworks lithium DENDRITE lithium SULFUR BATTERIES lithium oxygen BATTERIES li plating/stripping
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Lithium metal anodes: Present and future 被引量:19
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作者 Renheng Wang Weisheng Cui +1 位作者 Fulu Chu Feixiang Wu 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2020年第9期145-159,I0005,共16页
Commercial lithium-ion(Li-ion)batteries based on graphite anodes are meeting their bottlenecks that are limited energy densities.In order to satisfy the large market demands of smaller and lighter rechargeable batteri... Commercial lithium-ion(Li-ion)batteries based on graphite anodes are meeting their bottlenecks that are limited energy densities.In order to satisfy the large market demands of smaller and lighter rechargeable batteries,high-capacity metallic Li replacing low-specific-capacity graphite enables the higher energy density in next-generation rechargeable Li metal batteries(LMBs).However,Li metal anode has been suffering from dendritic problems,interfacial side reactions,volume change and low Coulombic efficiency.Therefore,performance enhancements of Li metal anodes are rather important to realize the high energy density characteristic of metallic Li.In this review,the annoying Li dendrite growth,unstable reaction interface and practical application issues of Li metal anodes are summarized and detailedly discussed to understand the current challenges concerning Li metal anodes.For overcoming such remaining challenges,the corresponding strategies and recent advances are covered and categorized.Finally,we discuss future opportunities and perspectives for developing high-performance Li metal anodes. 展开更多
关键词 lithium ANODE lithium metal battery Surface protection li dendrite
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Li/CF_(x)一次电池研究进展 被引量:1
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作者 汤才 蒋江民 +3 位作者 王新峰 刘广发 崔艳华 庄全超 《储能科学与技术》 CAS CSCD 北大核心 2023年第4期1093-1109,共17页
锂/氟化碳(Li/CF_(x))一次电池是目前能量密度最高的化学电源,具有输出电压稳定、安全性好、使用温度范围宽和自放电率低等特点,在军事(单兵作战系统)、医疗(心脏起搏器)、太空探索(空间站)等关键领域具有无可替代的重要性。然而,氟化... 锂/氟化碳(Li/CF_(x))一次电池是目前能量密度最高的化学电源,具有输出电压稳定、安全性好、使用温度范围宽和自放电率低等特点,在军事(单兵作战系统)、医疗(心脏起搏器)、太空探索(空间站)等关键领域具有无可替代的重要性。然而,氟化碳材料的电子导电性较差,很大程度地影响了电化学反应的电极过程动力学,导致Li/CF_(x)一次电池存在高倍率放电性能差、初始放电电压延迟严重、放电过程中发热量大等问题。本文通过对近期相关文献的探讨,首先综述了Li/CF_(x)一次电池在放电机理方面的研究进展,包括两相放电反应机理模型、生成石墨层间化合物中间相的放电反应机理模型、“核-壳”模型反应机理和边缘传播放电反应机理以及最近刚被提出的三步放电反应机理等。其次,重点分析了Li/CF_(x)一次电池面临问题的解决方法,包括氟化碳材料前驱体的选择、氟化方法的改进、复合材料的构建以及电解液的改性和优化方法。其中,氟化碳纳米管、氟化富勒烯、氟化石墨烯等新型氟化碳基材料的应用为氟化碳的发展提供了新的前景。在复合材料的构建策略上,导电聚合物、金属纳米颗粒、氧化物的加入可显著降低电压延迟时间和提升倍率性能。在电解液的调控策略上,氟离子结合剂的引入和氟化锂晶体生长动力学的计算,对于溶解氟化锂和控制氟化锂的生长具有重要作用,有望实现兼具高能量密度和高功率密度的宽温域Li/CF_(x)一次电池。 展开更多
关键词 锂/氟化碳(li/CF_(x))一次电池 氟化碳 反应机理 复合材料 电解液
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