Li3V2-2/3xMnx（PO4）3（0≤x≤0.12） powders were synthesized by sol-gel method. The effect of Mn2＋-doping on the structure and electrochemical performances of Li3V2（PO4）3/C was characterized by XRD, SEM, XPS, galva...Li3V2-2/3xMnx（PO4）3（0≤x≤0.12） powders were synthesized by sol-gel method. The effect of Mn2＋-doping on the structure and electrochemical performances of Li3V2（PO4）3/C was characterized by XRD, SEM, XPS, galvanostatic charge /discharge and electrochemical impedance spectroscopy（EIS）. The XRD study shows that a small amount of Mn2＋-doped does not alter the structure of Li3V2（PO4）3/C materials, and all Mn2＋-doped samples are of pure single phase with a monoclinic structure （space group P21/n）. The XPS analysis indicates that valences state of V and Mn are ＋3 and ＋2 in Li3V1.94Mn0.09（PO4）3/C, respectively, and the citric acid in raw materials was decomposed into carbon during calcination, and residual carbon exists in Li3V1.94Mn0.09（PO4）/C. The results of electrochemical measurements show that Mn2＋-doping can improve the cyclic stability and rate performance of these cathode materials. The Li3V1.94Mn0.09（PO4）3/C cathode material shows the best cyclic stability and rate performance. For example, at the discharge current density of 40 mA/g, after 100 cycles, the discharge capacity of Li3V1.94Mn0.09（PO4）3/C declines from initial 158.8 mA·h/g to 120.5 mA·h/g with a capacity retention of 75.9%; however, that of the Mn-undoed sample declines from 164.2 mA·h/g to 72.6 mA·h/g with a capacity retention of 44.2%. When the discharge current is increased up to 1C, the intial discharge capacity of Li3V1.94Mn0.09（PO4）3/C still reaches 146.4 mA·h/g, and the discharge capacity maintains at 107.5 mA·h/g after 100 cycles. The EIS measurement indicates that Mn2＋-doping with a appropriate amount of Mn2＋ decreases the charge transfer resistance, which is favorable for the insertion/extraction of Li＋.展开更多
LiFePO4-Li3V2（PO4）3 composites were synthesized by solid-hydrothermal method and by ball milling,respectively.The electrochemical performance of the solid-hydrothermally obtained materials（C-LFVP） was significantl...LiFePO4-Li3V2（PO4）3 composites were synthesized by solid-hydrothermal method and by ball milling,respectively.The electrochemical performance of the solid-hydrothermally obtained materials（C-LFVP） was significantly improved compared with LiFePO4（LFP） and Li3V2（PO4）3（LVP）,and it was also much better than that of the ball-milled LiFePO4-Li3V2（PO4）3（P-LFVP）.C-LFVP and P-LFVP both had four REDOX peaks（voltage plateaus）,which coincided with that of LFP and LVP.Some new trace substances were found in C-LFVP which had more perfect morphology,this was responsible for the better electrochemical performance of C-LFVP than P-LFVP.展开更多
2LiFe1-xCoxPO4-Li3V2（P04）3/C was synthesized using Fel-2xCo2xVO4 as precursor which was prepared by a simple co-precipitation method. 2LiFej-xCoxPO4-Li3V2（PO4）3/C samples were characterized by X-ray diffraction （...2LiFe1-xCoxPO4-Li3V2（P04）3/C was synthesized using Fel-2xCo2xVO4 as precursor which was prepared by a simple co-precipitation method. 2LiFej-xCoxPO4-Li3V2（PO4）3/C samples were characterized by X-ray diffraction （XRD）, scanning electron microscopy （SEM） and electrochemical measurements. All 2LiFel-xCoxPOa-Li3V2（PO4）3/C composites are of the similar crystal structure. The XRD analysis and SEM images show that 2LiFe0.96Co0.04PO4-Li3V2（PO4）3/C sample has the best-ordered structure and the smallest particle size. The charge-discharge tests demonstrate that these powders have the best electrochemical properties with an initial discharge capacity of 144.1 mA.h/g and capacity retention of 95.6% after 100 cycles when cycled at a current density of 0.1C between 2.5 and 4.5 V.展开更多
以聚吡咯(PVP K60)为表面活性剂和碳源,采用流变相法合成了x Li Fe PO4·y Li3V2(PO4)3/C正极材料样品。利用扫描电子显微镜(SEM)、X射线衍射仪(XRD)对样品形貌和结构进行了测试;采用电池测试仪和电化学工作站对样品电化学性能进行...以聚吡咯(PVP K60)为表面活性剂和碳源,采用流变相法合成了x Li Fe PO4·y Li3V2(PO4)3/C正极材料样品。利用扫描电子显微镜(SEM)、X射线衍射仪(XRD)对样品形貌和结构进行了测试;采用电池测试仪和电化学工作站对样品电化学性能进行了测试,分析了不同复合比(x:y)对其结构和电化学性能的影响。研究表明:复合材料中存在两相复合与元素掺杂两种效应;当复合比为5∶1时材料的电化学性能最优,在0.1和10 C倍率下放电容量分别达到162.7和104.6 m Ah·g-1,且具有良好的循环稳定性。展开更多
基金Project (20771100) supported by the National Natural Science Foundation of China
文摘Li3V2-2/3xMnx（PO4）3（0≤x≤0.12） powders were synthesized by sol-gel method. The effect of Mn2＋-doping on the structure and electrochemical performances of Li3V2（PO4）3/C was characterized by XRD, SEM, XPS, galvanostatic charge /discharge and electrochemical impedance spectroscopy（EIS）. The XRD study shows that a small amount of Mn2＋-doped does not alter the structure of Li3V2（PO4）3/C materials, and all Mn2＋-doped samples are of pure single phase with a monoclinic structure （space group P21/n）. The XPS analysis indicates that valences state of V and Mn are ＋3 and ＋2 in Li3V1.94Mn0.09（PO4）3/C, respectively, and the citric acid in raw materials was decomposed into carbon during calcination, and residual carbon exists in Li3V1.94Mn0.09（PO4）/C. The results of electrochemical measurements show that Mn2＋-doping can improve the cyclic stability and rate performance of these cathode materials. The Li3V1.94Mn0.09（PO4）3/C cathode material shows the best cyclic stability and rate performance. For example, at the discharge current density of 40 mA/g, after 100 cycles, the discharge capacity of Li3V1.94Mn0.09（PO4）3/C declines from initial 158.8 mA·h/g to 120.5 mA·h/g with a capacity retention of 75.9%; however, that of the Mn-undoed sample declines from 164.2 mA·h/g to 72.6 mA·h/g with a capacity retention of 44.2%. When the discharge current is increased up to 1C, the intial discharge capacity of Li3V1.94Mn0.09（PO4）3/C still reaches 146.4 mA·h/g, and the discharge capacity maintains at 107.5 mA·h/g after 100 cycles. The EIS measurement indicates that Mn2＋-doping with a appropriate amount of Mn2＋ decreases the charge transfer resistance, which is favorable for the insertion/extraction of Li＋.
基金Project (2007BAQ01055) supported by the National Key Technology R&D Programs of ChinaProject (50574063) supported by theNational Natural Science Foundation of China
文摘LiFePO4-Li3V2（PO4）3 composites were synthesized by solid-hydrothermal method and by ball milling,respectively.The electrochemical performance of the solid-hydrothermally obtained materials（C-LFVP） was significantly improved compared with LiFePO4（LFP） and Li3V2（PO4）3（LVP）,and it was also much better than that of the ball-milled LiFePO4-Li3V2（PO4）3（P-LFVP）.C-LFVP and P-LFVP both had four REDOX peaks（voltage plateaus）,which coincided with that of LFP and LVP.Some new trace substances were found in C-LFVP which had more perfect morphology,this was responsible for the better electrochemical performance of C-LFVP than P-LFVP.
基金Project(51072233) supported by National Natural Science Foundation of China
文摘2LiFe1-xCoxPO4-Li3V2（P04）3/C was synthesized using Fel-2xCo2xVO4 as precursor which was prepared by a simple co-precipitation method. 2LiFej-xCoxPO4-Li3V2（PO4）3/C samples were characterized by X-ray diffraction （XRD）, scanning electron microscopy （SEM） and electrochemical measurements. All 2LiFel-xCoxPOa-Li3V2（PO4）3/C composites are of the similar crystal structure. The XRD analysis and SEM images show that 2LiFe0.96Co0.04PO4-Li3V2（PO4）3/C sample has the best-ordered structure and the smallest particle size. The charge-discharge tests demonstrate that these powders have the best electrochemical properties with an initial discharge capacity of 144.1 mA.h/g and capacity retention of 95.6% after 100 cycles when cycled at a current density of 0.1C between 2.5 and 4.5 V.
基金supported by the Fund for Young Scientists of Sichuan University, China (2011SCU11081)Research Fund for the Doctoral Program of Higher Education, Ministry of Education of China (20120181120103)~~
文摘以聚吡咯(PVP K60)为表面活性剂和碳源,采用流变相法合成了x Li Fe PO4·y Li3V2(PO4)3/C正极材料样品。利用扫描电子显微镜(SEM)、X射线衍射仪(XRD)对样品形貌和结构进行了测试;采用电池测试仪和电化学工作站对样品电化学性能进行了测试,分析了不同复合比(x:y)对其结构和电化学性能的影响。研究表明:复合材料中存在两相复合与元素掺杂两种效应;当复合比为5∶1时材料的电化学性能最优,在0.1和10 C倍率下放电容量分别达到162.7和104.6 m Ah·g-1,且具有良好的循环稳定性。
