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Strategies of Removing Residual Lithium Compounds on the Surface of Ni-Rich Cathode Materials 被引量:7
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作者 Yuefeng Su Linwei Li +6 位作者 Gang Chen Lai Chen Ning Li Yun Lu Liying Bao Shi Chen Feng Wu 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2021年第1期189-198,共10页
Ni-rich cathode materials have become one of the most promising cathode materials for advanced high-energy Li-ion batteries(LIBs)owing to their high specific capacity.However,Ni-rich cathode materials are sensitive to... Ni-rich cathode materials have become one of the most promising cathode materials for advanced high-energy Li-ion batteries(LIBs)owing to their high specific capacity.However,Ni-rich cathode materials are sensitive to the trace H2O and CO2 in the air,and tend to react with them to generate LiOH and Li2COg at the particle surface region(named residual lithium compounds,labeled as RLCs).The RLCs will deteriorate the comprehensive performances of Ni-rich cathode materials and make trouble in the subsequent manufacturing process of electrode,including causing low initial coulombic efficiency and poor storage property,bringing about potential safety hazards,and gelatinizing the electrode slurry.Therefore,it is of considerable significance to remove the RLCs.Researchers have done a lot of work on the corresponding field,such as exploring the formation mechanism and elimination methods.This paper investigates the origin of the surface residual lithium compounds on Ni-rich cathode materials,analyzes their adverse effects on the per-formance and the subsequent electrode production process,and summarizes various kinds of feasible methods for removing the RLCS.Finally,we propose a new research direction of eliminating the lithium residuals after comparing and summing up the above.We hope this work can provide a reference for alleviating the adverse effects of residual lithium compounds for Ni-rich cathode materials'industrial production. 展开更多
关键词 Materials science Rechargeable battery lithium Ni-rich cathode material Residual lithium compounds
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Effect of chemical reactions between electrolyte and lithium compounds on the electrochemical performance of the ceramic fuel cells
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作者 Ruixin Dai Gang Chen +5 位作者 Kai Wei Zhuo Chen Xiaohong Lv Guoqiang Liu Ying Li Shujiang Geng 《Carbon Resources Conversion》 2022年第2期131-138,共8页
Previous studies have found that the ceramic fuel cell using Ni_(0.8)Co_(0.15)Al_(0.05)LiO_(2)(NCAL)symmetrical electrode has obtained very good power generation performance in the temperature range of 450 to 550℃.Pr... Previous studies have found that the ceramic fuel cell using Ni_(0.8)Co_(0.15)Al_(0.05)LiO_(2)(NCAL)symmetrical electrode has obtained very good power generation performance in the temperature range of 450 to 550℃.Previous studies have pointed out that after being reduced by H2,NCAL anode will produce LiOH/Li2CO3 mixture and diffuse into the electrolyte,which results in the high ionic conductivity of the cell.In this study,the chemical reactivity of different oxide electrolytes such as CeO_(2),TiO_(2),ZrO_(2)and YSZ with LiOH and/or Li2CO3 and their effects on the electrochemical performance of the cell were studied.It is found that at 550◦C,only the open circuit voltage(OCV)of the cell using CeO_(2)as electrolyte can remain stable,and the maximum power density(MPD)of the CeO_(2)electrolyte cell reaches 599.6 mW⋅cm^(−2).The OCV of the cells with TiO_(2),ZrO_(2)and YSZ as electrolyte increased to the highest value within a few minutes,and the MPD of the cells was only more than 12 mW⋅cm^(−2).XRD,FT-IR,SEM-EDS and ICP-OES results indicate that the LiOH/Li2CO3 mixture diffuses into TiO_(2),ZrO_(2)and YSZ electrolytes and reacts with three oxides to produce Li2TiO3 and Li2ZrO3,respectively,which results in the low performance of the cell. 展开更多
关键词 Ceramic fuel cell with lithium compounds ELECTRODE Ni_(0.8)Co_(0.15)Al_(0.05)LiO_(2) LiOH Chemical reaction Electrochemical performance
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Performance degradation mechanism of lithium compounds ceramic fuel cell with GDC as electrolyte 被引量:1
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作者 Kai Wei Rui Zhang +4 位作者 Gang Chen Zhuo Chen Ruixin Dai Xiaohong Lv Shujiang Geng 《Carbon Resources Conversion》 EI 2023年第3期238-244,共7页
The performance degradation mechanism of ceramic fuel cell with NCAL(Ni_(0.8)Co_(0.15)Al_(0.05)LiO_(2))as symmetrical electrode and GDC as electrolyte in H2 is investigated.It is found that under the condition of 550◦... The performance degradation mechanism of ceramic fuel cell with NCAL(Ni_(0.8)Co_(0.15)Al_(0.05)LiO_(2))as symmetrical electrode and GDC as electrolyte in H2 is investigated.It is found that under the condition of 550◦C and constant current density of 0.2 A⋅cm^(-2),the output voltage of the cell is about 1.005 V in the initial 10 h and remains relatively stable.After 10 h,the voltage of the cell began to decrease gradually,and by 50 h,the voltage had decreased to 0.522 V.The results testing electrochemical performance of the cell and characterizing the cell materials before and after test using SEM,TOF-SIMS and FTIR indicate that the distribution of Li_(2)O/LiOH/Li_(2)CO_(3)compounds generated from NCAL anode in the cell plays a vital role in significantly improving the ionic conductivity of electrolyte and gas tightness of the cell.The dynamic migration of molten salt destroyed the continuity of molten salt in the cell,which in turn adversely impacted the ionic conductivity of electrolyte,gas tightness of the cell,and electrochemical reactions on both sides of the cathode and anode.These finally lead to the degradation of the cell performance. 展开更多
关键词 Ceramic fuel cell Ni_(0.8)Co_(0.15)Al_(0.05)LiO_(2) Degradation mechanism lithium compound molten salt Dynamic migration
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Electrochemical performance of a nickel-rich LiNi0.6Co0.2Mn0.2O2 cathode material for lithium-ion batteries under different cut-off voltages 被引量:14
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作者 Kai-lin Cheng Dao-bin Mu +3 位作者 Bo-rong Wu Lei Wang Ying Jiang Rui Wang 《International Journal of Minerals,Metallurgy and Materials》 SCIE EI CAS CSCD 2017年第3期342-351,共10页
A spherical-like Ni0.6Co0.2Mn0.2(OH)2precursor was tuned homogeneously to synthesize LiNi0.6Co0.2Mn0.2O2as a cathode material for lithium-ion batteries. The effects of calcination temperature on the crystal structure,... A spherical-like Ni0.6Co0.2Mn0.2(OH)2precursor was tuned homogeneously to synthesize LiNi0.6Co0.2Mn0.2O2as a cathode material for lithium-ion batteries. The effects of calcination temperature on the crystal structure, morphology, and the electrochemical performance of the as-prepared LiNi0.6Co0.2Mn0.2O2were investigated in detail. The as-prepared material was characterized by X-ray diffraction, scanning electron microscopy, laser particle size analysis, charge–discharge tests, and cyclic voltammetry measurements. The results show that the spherical-like LiNi0.6Co0.2Mn0.2O2material obtained by calcination at 900°C displayed the most significant layered structure among samples calcined at various temperatures, with a particle size of approximately 10 μm. It delivered an initial discharge capacity of 189.2 mAh•g−1at 0.2C with a capacity retention of 94.0% after 100 cycles between 2.7 and 4.3 V. The as-prepared cathode material also exhibited good rate performance, with a discharge capacity of 119.6 mAh•g−1at 5C. Furthermore, within the cut-off voltage ranges from 2.7 to 4.3, 4.4, and 4.5 V, the initial discharge capacities of the calcined samples were 170.7, 180.9, and 192.8 mAh•g−1, respectively, at a rate of 1C. The corresponding retentions were 86.8%, 80.3%, and 74.4% after 200 cycles, respectively. © 2017, University of Science and Technology Beijing and Springer-Verlag Berlin Heidelberg. 展开更多
关键词 CALCINATION Cathodes Cobalt Crystal structure Cyclic voltammetry Electric batteries Electric discharges Electrochemical properties Electrodes Ions lithium lithium alloys lithium compounds Manganese NICKEL Particle size Particle size analysis Scanning electron microscopy Secondary batteries X ray diffraction
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LiPF6 and lithium difluoro(oxalato)borate/ethylene carbonate+dimethyl carbonate+ethyl(methyl)carbonate electrolyte for LiNi0.5Mn1.5O4 cathode 被引量:2
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作者 ZHOU Hong-ming GENG Wen-jun LI Jian 《Journal of Central South University》 SCIE EI CAS CSCD 2017年第5期1013-1018,共6页
LiODFB electrolyte’s compatibility with LiNi0.5Mn1.5O4high-voltage cathode material was studied by cyclic voltammetry, charge-discharge test and AC impedance. The results show that at 25 and 60 °C, the LiODFB-ba... LiODFB electrolyte’s compatibility with LiNi0.5Mn1.5O4high-voltage cathode material was studied by cyclic voltammetry, charge-discharge test and AC impedance. The results show that at 25 and 60 °C, the LiODFB-based electrolyte has better electrochemical stability than LiPF6. AC impedance plots show that the LiODFB battery has a lower charge-transfer resistance than LiPF6battery at 60 °C, which indicates that LiODFB battery has excellent cycling performance at high temperature. At 25 and 60 °C, the LiNi0.5Mn1.5O4/Li half cells with LiODFB or LiPF6as electrolyte all have simple redox peak, showing that each of them has an excellent reversibility. LiODFB battery has better cycle performance than LiPF6battery at 25 °C and 60 °C. At 25 °C, their 0.5C initial discharge specific capacities are 126.3 and 131.6 mA·h/g, and their capacity retention ratios of the 100th cycle are 97.1% and 94.7%, respectively. At 60 °C, their 0.5C initial discharge specific capacities are 132.6 and 129.1 mA·h/g, and their capacity retention ratios of the 100th cycle are 94.1% and 81.7%, respectively. © 2017, Central South University Press and Springer-Verlag GmbH Germany. 展开更多
关键词 CARBONATION Cathodes Charge transfer Cyclic voltammetry Electric batteries Electric discharges Electric impedance Electrodes Electrolytes lithium compounds Manganese
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FePO4-coated Li[Li0.2Ni0.13Co0.13Mn0.54]O2 with improved cycling performance as cathode material for Li-ion batteries 被引量:4
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作者 Zhong Wang Hua-Quan Lu +5 位作者 Yan-Ping Yin Xue-Yi Sun Xiang-Tao Bai Xue-Ling Shen Wei-Dong Zhuang Shi-Gang Lu 《Rare Metals》 SCIE EI CAS CSCD 2017年第11期899-904,共6页
Li[Li0.2Ni0.13Coo.13Mn0.54]O2 cathode materials were synthesized by carbonate-based co-precipitation method, and then, its surface was coated by thin layers of FePO4. The prepared samples were characterized by X-ray d... Li[Li0.2Ni0.13Coo.13Mn0.54]O2 cathode materials were synthesized by carbonate-based co-precipitation method, and then, its surface was coated by thin layers of FePO4. The prepared samples were characterized by X-ray diffraction (XRD), field emission scanning electron micro- scope (FESEM), energy-dispersive spectroscopy (EDS), and transmission electron microscopy (TEM). The XRD and TEM results suggest that both the pristine and the coated materials have a hexagonal layered structure, and the FePO4 coating layer does not make any major change in the crystal structure. The FePO4-coated sample exhibits both improved initial discharge capacity and columbic efficiency compared to the pristine one. More significantly, the FePO4 coating layer has a much positive influence on the cycling perfor- mance. The FePO4-coated sample exhibits capacity reten- tion of 82 % after 100 cycles at 0.5℃ between 2.0 and 4.8 V, while only 28 % for the pristine one at the same charge-discharge condition. The electrochemical impe- dance spectroscopy (EIS) results indicate that this improved cycling performance could be ascribed to the presence of FePO4 on the surface of Li[Li0.2Ni0.13Co0.13Mno.54102 par- ticle, which helps to protect the cathode from chemical attacks by HF and thus suppresses the large increase in charge transfer resistance. 展开更多
关键词 Cathodes Charge transfer Coated materials Coatings Crystal structure Electric batteries Electrochemical impedance spectroscopy Electrodes Energy dispersive spectroscopy Field emission cathodes High resolution transmission electron microscopy lithium lithium alloys lithium compounds Manganese Nickel Precipitation (chemical) Scanning electron microscopy Secondary batteries Transmission electron microscopy X ray diffraction
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Alkali-Silica Reaction Inhibited by LiOH and Its Mechanism 被引量:2
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作者 莫祥银 《Journal of Wuhan University of Technology(Materials Science)》 SCIE EI CAS 2003年第1期13-16,共4页
A high alkali reactive aggregate zeolitization perlite was used to test the long term effectiveness of LiOH in inhibiting alkali silica reaction.In this paper,the rigorous conditions were designed that the mortar b... A high alkali reactive aggregate zeolitization perlite was used to test the long term effectiveness of LiOH in inhibiting alkali silica reaction.In this paper,the rigorous conditions were designed that the mortar bars had been cured at 80℃ for 3 years after autoclaved 24 hours at 150℃.Under this condition,LiOH was able to inhibit the alkali silica reaction long term effectiveness.Not only the relationship between the molar ratio of n(Li)/(Na) and the alkali contents in systems was established, but also the governing mechanism of such effects was also studied by SEM. 展开更多
关键词 lithium compounds alkali silica reaction long term performance MECHANISM
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Cascaded Raman lasing in a lithium tetraborate whispering gallery mode resonator
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作者 CHENGCAI TIAN JERVEE PUNZALAN +5 位作者 PETRA BECKER LADISLAV BOHATÝ KEITH C.GORDON RICHARD BLAIKIE HARALD G.L.SCHWEFEL FLORIAN SEDLMEIR 《Photonics Research》 2025年第8期2232-2239,共8页
Lithium tetraborate(LB4)is a lithium borate compound known for its exceptional linear and nonlinear optical properties,including a wide transparency range(0.16–3.5μm)and high Raman gain.Here,a millimeter-sized LB4 w... Lithium tetraborate(LB4)is a lithium borate compound known for its exceptional linear and nonlinear optical properties,including a wide transparency range(0.16–3.5μm)and high Raman gain.Here,a millimeter-sized LB4 whispering gallery mode(WGM)resonator with a record quality factor of 2.0×10^(9) at 517 nm was fabricated using single-point diamond cutting.Pumped with about 10 m W at 517 nm,it demonstrated four cascaded stimulated Raman scattering(SRS)peaks(537–608 nm),with the first-order SRS achieving a threshold of 0.71 m W and 7.2% slope efficiency.To our knowledge,this marks the first LB4 WGM resonator Raman laser. 展开更多
关键词 stimulated Raman scattering whispering gallery mode wgm resonator lithium tetraborate lb cascaded Raman lasing cascaded stimulated raman scattering srs peaks whispering gallery mode resonator Raman gain lithium borate compound
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Theoretical study of quasi-phase-matching fourth harmonic generation in periodically poled lithium tantalate 被引量:1
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作者 谢威 陈险峰 +2 位作者 何利科 陈玉萍 夏宇兴 《Chinese Optics Letters》 SCIE EI CAS CSCD 2004年第11期664-666,共3页
The direct fourth harmonic generation (FHG) is theoretically demonstrated based on quasi-phase-matching (QPM) configuration in periodically poled lithium tantalate (PPLT). The wavelength dependence of the period of FH... The direct fourth harmonic generation (FHG) is theoretically demonstrated based on quasi-phase-matching (QPM) configuration in periodically poled lithium tantalate (PPLT). The wavelength dependence of the period of FHG QPM gratings is calculated. Bandwidths of fundamental wavelength, temperature, and incident angle are also studied. A very wide bandwidth, as large as 119.5 nm, of fundamental wavelength near 3699 nm is found with the QPM period of 9.442 μm and the crystal length of 1 cm. 展开更多
关键词 BANDWIDTH Harmonic generation lithium compounds
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Efficiency-enhanced picosecond mid-infrared optical parametric downconversion based on a cascaded optical superlattice 被引量:3
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作者 李世凤 居盼盼 +5 位作者 刘艳花 蒋旭东 倪睿 赵刚 吕新杰 祝世宁 《Chinese Optics Letters》 SCIE EI CAS CSCD 2016年第4期39-41,共3页
We demonstrate an efficiency-enhanced picosecond (ps) mid-infrared radiation via optical parametric downconversion. Based on a cascaded periodically poled MgO-doped stoiehiometric lithium tantalate crystal (MgO:sP... We demonstrate an efficiency-enhanced picosecond (ps) mid-infrared radiation via optical parametric downconversion. Based on a cascaded periodically poled MgO-doped stoiehiometric lithium tantalate crystal (MgO:sPPLT), a tandem optical parametric oscillation-optical parametric amplification (OPO-OPA) process is achieved. Compared with a single OPO process, the conversion efficiency obtains an enhancement of 71%. 展开更多
关键词 EFFICIENCY Infrared devices Infrared radiation lithium compounds Optical frequency conversion
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