Lithium primary batteries are widely used in various fields where high energy densities and long storage times are in demand.However,studies on lithium primary batteries are currently focused on the gravimetric energy...Lithium primary batteries are widely used in various fields where high energy densities and long storage times are in demand.However,studies on lithium primary batteries are currently focused on the gravimetric energy densities of active materials and rarely account for the volumetric energy requirements of unmanned devices.Herein,CuF_(2)/CF_(x) composites are prepared via planetary ball milling(PBM)to improve the volumetric energy densities of lithium primary batteries using the high mass density of CuF_(2),achieving a maximum volumetric energy density of 4163.40 Wh L^(-1).The CuF_(2)/CF_(x) hybrid cathodes exhibit three distinct discharge plateaus rather than simple combinations of the discharge curves of their components.This phenomenon is caused by charge redistribution and lattice modulation on the contact surfaces of CuF_(2) and CF_(x) during PBM,which change the valence state of Cu and modify the electronic structures of the composites.As a result,CuF_(2)/CF_(x) hybrid cathodes exhibit unique discharge behaviors and improved rate capabilities,delivering a maximum power density of 11.16 kW kg^(-1)(25.56 kW L^(-1)).Therefore,it is a promising strategy to further improve the comprehensive performance of lithium primary batteries through the use of interfacial optimization among different fluoride cathodes.展开更多
In order to confirm the optimal Li content of Li-rich Mn-based cathode materials(a fixed mole ratio of Mn to Ni to Co is0.6:0.2:0.2),Li1+x(Mn0.6Ni0.2Co0.2)1-xO2(x=0,0.1,0.2,0.3)composites were obtained,which had a typ...In order to confirm the optimal Li content of Li-rich Mn-based cathode materials(a fixed mole ratio of Mn to Ni to Co is0.6:0.2:0.2),Li1+x(Mn0.6Ni0.2Co0.2)1-xO2(x=0,0.1,0.2,0.3)composites were obtained,which had a typical layered structure with R3m and C2/m space group observed from X-ray powder diffraction(XRD).Electron microscopy micrograph(SEM)reveals that the particle sizes in the range of0.4-1.1μm increase with an increase of x value.Li1.2(Mn0.6Ni0.2Co0.2)0.8O2sample delivers a larger initial discharge capacity of275.7mA·h/g at the current density of20mA/g in the potential range of2.0-4.8V,while Li1.1(Mn0.6Ni0.2Co0.2)0.9O2shows a better cycle performance with a capacity retention of93.8%at0.2C after50cycles,showing better reaction kinetics of lithium ion insertion and extraction.展开更多
Recently,poly(ethylene oxide)(PEO)-based solid polymer electrolytes have been attracting great attention,and efforts are currently underway to develop PEO-based composite electrolytes for next generation high performa...Recently,poly(ethylene oxide)(PEO)-based solid polymer electrolytes have been attracting great attention,and efforts are currently underway to develop PEO-based composite electrolytes for next generation high performance all-solid-state lithium metal batteries.In this article,a novel sandwich structured solid-state PEO composite electrolyte is developed for high performance all-solid-state lithium metal batteries.The PEO-based composite electrolyte is fabricated by hot-pressing PEO,LiTFSI and Ti_(3)C_(2)T_(x) MXene nanosheets into glass fiber cloth(GFC).The as-prepared GFC@PEO-MXene electrolyte shows high mechanical properties,good electrochemical stability,and high lithium-ion migration number,which indicates an obvious synergistic effect from the microscale GFC and the nanoscale MXene.Such as,the GFC@PEO-1 wt%MXene electrolyte shows a high tensile strength of 43.43 MPa and an impressive Young's modulus of 496 MPa,which are increased by 1205%and 6048%over those of PEO.Meanwhile,the ionic conductivity of GFC@PEO-1 wt%MXene at 60℃ reaches 5.01×10^(-2) S m^(-1),which is increased by around 200%compared with that of GFC@PEO electrolyte.In addition,the Li/Li symmetric battery based on GFC@PEO-1 wt%MXene electrolyte shows an excellent cycling stability over 800 h(0.3 mA cm^(-2),0.3 mAh cm^(-2)),which is obviously longer than that based on PEO and GFC@PEO electrolytes due to the better compatibility of GFC@PEO-1 wt%MXene electrolyte with Li anode.Furthermore,the solid-state Li/LiFePO_(4) battery with GFC@PEO-1 wt%MXene as electrolyte demonstrates a high capacity of 110.2–166.1 mAh g^(-1) in a wide temperature range of 25–60C,and an excellent capacity retention rate.The developed sandwich structured GFC@PEO-1 wt%MXene electrolyte with the excellent overall performance is promising for next generation high performance all-solid-state lithium metal batteries.展开更多
The cathode material Li 1+ x Mn 2O 4 was prepared by a modified citric acid complexation method. The influences of temperature, sintering time and n (Li)/ n (Mn) ratio on the structure of the products have been explor...The cathode material Li 1+ x Mn 2O 4 was prepared by a modified citric acid complexation method. The influences of temperature, sintering time and n (Li)/ n (Mn) ratio on the structure of the products have been explored, characterized and tested by XRD, TEM, BET measurements. The sample sintered at 750 ℃ for 12 h had greater charge/discharge capacity, better cyclic stability under electric current charge/discharge cycle. The initial capacity reached 120 mA·h/g with the charge/discharge efficieney of 98% and maintained 115 mA·h/g after 50 cycles.展开更多
以 L i2 CO3 和 NH4 VO3 为原料 ,低温合成了 L i1+ x V3 O8.通过对中间产物的热分析 ,选定了低温合成 L i1+ x V3 O8的适宜煅烧温度为 30 0℃ .研究表明 ,L i1+ x V3 O8,原料 L i/ V摩尔比应大于1∶ 3.以 Li1+ x V3 O8作为正极材料 ,...以 L i2 CO3 和 NH4 VO3 为原料 ,低温合成了 L i1+ x V3 O8.通过对中间产物的热分析 ,选定了低温合成 L i1+ x V3 O8的适宜煅烧温度为 30 0℃ .研究表明 ,L i1+ x V3 O8,原料 L i/ V摩尔比应大于1∶ 3.以 Li1+ x V3 O8作为正极材料 ,金属锂为负极组装了模拟电池 ,高、低温合成材料具有较高的放电容量和放电电压 .XRD、SEM分析结果说明低温合成样品的结晶度低、粒径较小 .展开更多
基金financially supported by the National Key R&D Program of China(No.2016YFA0202302)the State Key Program of National Natural Science Foundation of China(Nos.51633007 and 52130303)the National Natural Science Foundation of China(Nos.51773147 and 51973151).
文摘Lithium primary batteries are widely used in various fields where high energy densities and long storage times are in demand.However,studies on lithium primary batteries are currently focused on the gravimetric energy densities of active materials and rarely account for the volumetric energy requirements of unmanned devices.Herein,CuF_(2)/CF_(x) composites are prepared via planetary ball milling(PBM)to improve the volumetric energy densities of lithium primary batteries using the high mass density of CuF_(2),achieving a maximum volumetric energy density of 4163.40 Wh L^(-1).The CuF_(2)/CF_(x) hybrid cathodes exhibit three distinct discharge plateaus rather than simple combinations of the discharge curves of their components.This phenomenon is caused by charge redistribution and lattice modulation on the contact surfaces of CuF_(2) and CF_(x) during PBM,which change the valence state of Cu and modify the electronic structures of the composites.As a result,CuF_(2)/CF_(x) hybrid cathodes exhibit unique discharge behaviors and improved rate capabilities,delivering a maximum power density of 11.16 kW kg^(-1)(25.56 kW L^(-1)).Therefore,it is a promising strategy to further improve the comprehensive performance of lithium primary batteries through the use of interfacial optimization among different fluoride cathodes.
基金Project(2018RS3091) supported by the Hunan Innovation Team,ChinaProjects(52202308, 12105097) supported by the National Natural Science Foundation of ChinaProject(2021RC2092) supported by the Science and Technology Innovation Program of Hunan Province,China。
基金Project(21473258) supported by the National Natural Science Foundation of ChinaProject(13JJ1004) supported by Distinguished Young Scientists of Hunan Province,ChinaProject(NCET-11-0513) supported by Program for the New Century Excellent Talents in University,China
文摘In order to confirm the optimal Li content of Li-rich Mn-based cathode materials(a fixed mole ratio of Mn to Ni to Co is0.6:0.2:0.2),Li1+x(Mn0.6Ni0.2Co0.2)1-xO2(x=0,0.1,0.2,0.3)composites were obtained,which had a typical layered structure with R3m and C2/m space group observed from X-ray powder diffraction(XRD).Electron microscopy micrograph(SEM)reveals that the particle sizes in the range of0.4-1.1μm increase with an increase of x value.Li1.2(Mn0.6Ni0.2Co0.2)0.8O2sample delivers a larger initial discharge capacity of275.7mA·h/g at the current density of20mA/g in the potential range of2.0-4.8V,while Li1.1(Mn0.6Ni0.2Co0.2)0.9O2shows a better cycle performance with a capacity retention of93.8%at0.2C after50cycles,showing better reaction kinetics of lithium ion insertion and extraction.
基金support of the Fundamental Research Funds for the Central Universities(No.2022CDJQY-004)the Fund for Innovative Research Groups of Natural Science Foundation of Hebei Province(No.A2020202002).
文摘Recently,poly(ethylene oxide)(PEO)-based solid polymer electrolytes have been attracting great attention,and efforts are currently underway to develop PEO-based composite electrolytes for next generation high performance all-solid-state lithium metal batteries.In this article,a novel sandwich structured solid-state PEO composite electrolyte is developed for high performance all-solid-state lithium metal batteries.The PEO-based composite electrolyte is fabricated by hot-pressing PEO,LiTFSI and Ti_(3)C_(2)T_(x) MXene nanosheets into glass fiber cloth(GFC).The as-prepared GFC@PEO-MXene electrolyte shows high mechanical properties,good electrochemical stability,and high lithium-ion migration number,which indicates an obvious synergistic effect from the microscale GFC and the nanoscale MXene.Such as,the GFC@PEO-1 wt%MXene electrolyte shows a high tensile strength of 43.43 MPa and an impressive Young's modulus of 496 MPa,which are increased by 1205%and 6048%over those of PEO.Meanwhile,the ionic conductivity of GFC@PEO-1 wt%MXene at 60℃ reaches 5.01×10^(-2) S m^(-1),which is increased by around 200%compared with that of GFC@PEO electrolyte.In addition,the Li/Li symmetric battery based on GFC@PEO-1 wt%MXene electrolyte shows an excellent cycling stability over 800 h(0.3 mA cm^(-2),0.3 mAh cm^(-2)),which is obviously longer than that based on PEO and GFC@PEO electrolytes due to the better compatibility of GFC@PEO-1 wt%MXene electrolyte with Li anode.Furthermore,the solid-state Li/LiFePO_(4) battery with GFC@PEO-1 wt%MXene as electrolyte demonstrates a high capacity of 110.2–166.1 mAh g^(-1) in a wide temperature range of 25–60C,and an excellent capacity retention rate.The developed sandwich structured GFC@PEO-1 wt%MXene electrolyte with the excellent overall performance is promising for next generation high performance all-solid-state lithium metal batteries.
文摘The cathode material Li 1+ x Mn 2O 4 was prepared by a modified citric acid complexation method. The influences of temperature, sintering time and n (Li)/ n (Mn) ratio on the structure of the products have been explored, characterized and tested by XRD, TEM, BET measurements. The sample sintered at 750 ℃ for 12 h had greater charge/discharge capacity, better cyclic stability under electric current charge/discharge cycle. The initial capacity reached 120 mA·h/g with the charge/discharge efficieney of 98% and maintained 115 mA·h/g after 50 cycles.
文摘以 L i2 CO3 和 NH4 VO3 为原料 ,低温合成了 L i1+ x V3 O8.通过对中间产物的热分析 ,选定了低温合成 L i1+ x V3 O8的适宜煅烧温度为 30 0℃ .研究表明 ,L i1+ x V3 O8,原料 L i/ V摩尔比应大于1∶ 3.以 Li1+ x V3 O8作为正极材料 ,金属锂为负极组装了模拟电池 ,高、低温合成材料具有较高的放电容量和放电电压 .XRD、SEM分析结果说明低温合成样品的结晶度低、粒径较小 .
