通过简单的溶胶-凝胶辅助静电纺丝法得到(113)晶面优势导向的Na_3V_2(PO_4)_3/C钠离子电池正极材料,并通过对比最佳纺丝条件下分别用聚乙烯吡咯烷酮(PVP)和聚氧化乙烯(PEO)作为晶面导向剂制备的两种Na_3V_2(PO_4)_3电极材料的电化学性能...通过简单的溶胶-凝胶辅助静电纺丝法得到(113)晶面优势导向的Na_3V_2(PO_4)_3/C钠离子电池正极材料,并通过对比最佳纺丝条件下分别用聚乙烯吡咯烷酮(PVP)和聚氧化乙烯(PEO)作为晶面导向剂制备的两种Na_3V_2(PO_4)_3电极材料的电化学性能,证明静电纺丝有利于实现Na_3V_2(PO_4)_3(113)晶面择优取向。在相同的电流密度(0.1 C)下,NVP-PVP和NVP-PEO的首周放电比容量分别为112.5 m A·h/g和96.3 m A·h/g,电池循环50周后,NVP-PVP仍然有98.1 m A·h/g的可逆容量保持,NVP-PEO仅仅只剩下34 m A·h/g的可逆容量保持,而即使循环100周后,NVP-PVP的可逆容量仍然在88.2 m A·h/g。结果表明,PVP静电纺丝有利于构建特定的纳米纤维结构和均一的导电碳网络骨架,进而提升主体材料Na_3V_2(PO_4)_3的电化学性能。展开更多
Sodium-ion batteries （SIBs） have attracted increasing attention in the past decades, because of high over-all abundance of precursors, their even geographical distribution, and low cost. Na3V2（PO4）3 （NVP）, atypi...Sodium-ion batteries （SIBs） have attracted increasing attention in the past decades, because of high over-all abundance of precursors, their even geographical distribution, and low cost. Na3V2（PO4）3 （NVP）, atypical sodium super ion conductor （NASlCON）-based electrode material, exhibits pronounced structuralstability, exceptionally high ion conductivity, rendering it a most promising electrode for sodium storage.However. the comparatively low electronic conductivity makes the theoretical capacity of NVP cannot befully accessible even at comparatively low rates, presenting a major drawback for further practical ap-plications, especially when high rate capability is especially important. Thus, many endeavors have beenconformed to increase the surface and intrinsic electrical conductivity of NVP by coating the active mate-rials with a conductive carbon layer, downsizing the NVP particles, combining the NVP particle with vari-ous carbon materials and ion doping strategy. In this review, to get a better understanding on the sodiumstorage in NVP, we firstly present 4 distinct crystal structures in the temperature range of-30℃-225℃ namely α-NVP, β-NVP, β′-NVP and γ-NVP. Moreover, we give an overview of recent approaches to en-hance the surface electrical conductivity and intrinsic electrical conductivity of NVP. Finally, some poten-tial applications of NVP such as in all-climate environment and PHEV, EV fields have been prospected.展开更多
NASICON (Na-super-ionic-conductors)-structured materials have attracted extensive research interest due to their great application potential in secondary batteries. However, the mechanism of capacity fading for NASICO...NASICON (Na-super-ionic-conductors)-structured materials have attracted extensive research interest due to their great application potential in secondary batteries. However, the mechanism of capacity fading for NASICON-structured electrode materials has been rarely studied. In this paper, we synthesized the NASICON-structured Na3V2(PO4)3/C composite by simple sol-gel and high-temperature solid-phase method and investigated its electrochemical performance in Na-Zn hybrid aqueous rechargeable batteries. After characterizing the structure, morphology and composition variations as well as the interfacial resistance changes of Na3V2(PO4)3/C cathode during cycling, we propose a mechanical and interfacial degradation mechanism for capacity fading of NASICON-structured Na3V2(PO4)3/C in Na-Zn hybrid aqueous rechargeable batteries. This work will shed light on enhancing the mechanical and in terfacial stability of NASICON-structured Na3V2(PO4)3/C in Na-Zn hybrid aqueous rechargeable batteries.展开更多
The rational assembly of quantum dots on two-dimensional(2 D) carbonaceous materials is very promising to produce materials, but remains a challenge. Here, we develop an assembly strategy of growing Na3 V2(PO4)3 quant...The rational assembly of quantum dots on two-dimensional(2 D) carbonaceous materials is very promising to produce materials, but remains a challenge. Here, we develop an assembly strategy of growing Na3 V2(PO4)3 quantum dots with superlattice structure(NVP-QDs-SL) for obtaining precise control of the size, distribution and crystallinity. The multifunctional lignocelluloses(LCs) used as a hard carbon source induce heterogeneous nucleation and confined growth of NVP-QDs-SL, leading to the uniform distribution of NVP-QDs-SL in H/S-doped hard carbon ultra-thin nanosheets(HCS). Detailed electrochemical analysis results from sodium-ion batteries of NVP-QDs-SL show that NVP-QDs-SL could trap the electrons inside HCS, significantly enhancing Na ion storage and transfer kinetics. Compared to the common Na3 V2(PO4)3 nanoparticle cathode, the NVP-QDs-SL/HCS cathode exhibits a high reversible capacity of 149.2 m A h g^-1 at a 0.1 C rate, which is far beyond the theoretical capacity of Na3 V2(PO4)3(117.6 m A h g^-1).At the ultrahigh current rate of 100 C, this cathode still remains a high discharge capacity of 40 m A h g-1.Even after cycling at 20 C over 3000 cycles, an ultrahigh coulombic efficiency close to 100% is still obtained,highlighting its excellent long cycling life, remarkable rate performance and energy density.展开更多
Na_(3)V_(2)(PO_(4))_(3)(NVP)cathode material of the sodium ion battery(1 C=117 mAh g-1)has a NASICON-type structure,which not only facilitates the rapid migration of sodium ions,but also has a small volume deformation...Na_(3)V_(2)(PO_(4))_(3)(NVP)cathode material of the sodium ion battery(1 C=117 mAh g-1)has a NASICON-type structure,which not only facilitates the rapid migration of sodium ions,but also has a small volume deformation during sodium ion de-intercalation and the main frame mechanism remains unchanged,and thus is seen as an energy storage material for a wide range of applications,but has a limited electronic conductivity due to its structure.In this paper,NVP cathode materials with finer primary particles are successfully prepared using a simple hydrothermal treatment-assisted sol-gel method.The increased pore size of the NVP materials prepared under the hydrothermal process allows for more active sites and more effective resistance to the volume deformation of sodium ions during insertion/extraction processes,effectively facilitating the diffusion of ions and electrons.The Na_(3)V_(2)(PO_(4))_(3) material obtained by the optimized process exhibited good crystallinity in XRD characterization,as well as superior electrochemical properties in a series of electrochemical tests.A specific capacitance of 106.3 mAh g^(-1) at 0.2 C is demonstrated,compared to 96.5 mAh g^(-1) for Na_(3)V_(2)(PO_(4))_(3) without hydrothermal treatment,and cycling performance is also improved with 93%capacity retention.The calculated sodium ion diffusion coefficient(DNa=5.68×10^(-14))obtained after EIS curve fitting of the improved sample illustrates that the pore structure is beneficial to the performance of the Na_(3)V_(2)(PO_(4))_(3)cathode material.展开更多
采用溶胶凝胶-高温固相法,用不同的钠源制备NASICON结构钠离子电池正极材料Na_3V_2(PO_4)_3.借助扫描电子显微镜(SEM),X射线衍射分析(XRD),电池测试系统及电化学工作站对制备的Na_3V_2(PO_4)_3结构,形貌,电性能和内阻进行表征.研究结果...采用溶胶凝胶-高温固相法,用不同的钠源制备NASICON结构钠离子电池正极材料Na_3V_2(PO_4)_3.借助扫描电子显微镜(SEM),X射线衍射分析(XRD),电池测试系统及电化学工作站对制备的Na_3V_2(PO_4)_3结构,形貌,电性能和内阻进行表征.研究结果表明,以Na_2CO_3为钠源合成Na_3V_2(PO_4)_3有更好的颗粒尺寸,形貌结构完整,充放电性能及循环稳定性更好,阻抗也较小;在2.5~4.0 V电压范围内,以0.2C进行充放电,首次放电比容量达到110.8 m Ah/g,50次循环后容量保持率为85.1%.展开更多
One main challenge for phosphate cathodes in sodium-ion batteries(SIBs)is to increase the working voltage and energy density to promote its practicability.Herein,an advanced Na3V2(PO4)2F3@C cathode is prepared success...One main challenge for phosphate cathodes in sodium-ion batteries(SIBs)is to increase the working voltage and energy density to promote its practicability.Herein,an advanced Na3V2(PO4)2F3@C cathode is prepared successfully for sodium-ion full cells.It is revealed that,carbon coating can not only enhance the electronic conductivity and electrode kinetics of Na3V2(PO4)2F3@C and inhibit the growth of particles(i.e.,shorten the Na^+-migration path),but also unexpectedly for the first time adjust the dis-/charging plateaux at different voltage ranges to increase the mean voltage(from 3.59 to 3.71 V)and energy density from 336.0 to 428.5 Wh kg^-1 of phosphate cathode material.As a result,when used as cathode for SIBs,the prepared Na3V2(PO4)2F3@C delivers much improved electrochemical properties in terms of larger specifc capacity(115.9 vs.93.5 mAh g^-1),more outstanding high-rate capability(e.g.,87.3 vs.60.5 mAh g^-1 at 10 C),higher energy density,and better cycling performance,compared to pristine Na3V2(PO4)2F3.Reasons for the enhanced electrochemical properties include ionicity enhancement of lattice induced by carbon coating,improved electrode kinetics and electronic conductivity,and high stability of lattice,which is elucidated clearly through the contrastive characterization and electrochemical studies.Moreover,excellent energy-storage performance in sodium-ion full cells further demonstrate the extremely high possibility of Na3V2(PO4)2F3@C cathode for practical applications.展开更多
Na superionic conductor (NASICON)-type Na3V2(PO4)3 (NVP) has been regarded as a promising cathode material for sodium-ion batteries (SIBs). However, NVP suffers from poor cyclability and rate capability because of its...Na superionic conductor (NASICON)-type Na3V2(PO4)3 (NVP) has been regarded as a promising cathode material for sodium-ion batteries (SIBs). However, NVP suffers from poor cyclability and rate capability because of its intrinsically low electronic conductivity. Herein, we successfully syn thesized N-doped carb on-wrapped Na3V2(PO4)3 (NC@NVP) through the carb on izati on of polydopami ne, which is rich in nitrogen species. The strong adhesion properties of the polydopamine lead to effective and homogeneous wrapping of NVP particles, and it I is further turned into a con ductive N-doped carb on n etwork itself, providi ng facile diffusi on of electr ons and Na+ i ons duri ng battery operation. NC@NVP displays remarkable electrochemical performanee, even under harsh operating conditions, such as a high rate capability (discharge capacity of 70.88, 49.21 mA·h·g^-1 at 50 and 100 C), long-term cycling stability (capacity retention of 94.77% over 1,000 cycles at 20 C), and high-temperature cycling (capacity retention of 92.0% after 500 cycles at 60 ℃).展开更多
In this study,a pseudo-layered Na super-ionic conductor of Na3V2(PO4)2F3 (NVPF)/C cathode for sodium-ion batteries is prepared successfully using a facile polyol refluxing process without any impurity phases.The X-ray...In this study,a pseudo-layered Na super-ionic conductor of Na3V2(PO4)2F3 (NVPF)/C cathode for sodium-ion batteries is prepared successfully using a facile polyol refluxing process without any impurity phases.The X-ray diffraction and Rietveld refinement results confirm that NVPF possesses tetragonal NASICON-type lattice with a space group of P42/mnm.In this preparative method,polyol is utilized as a solvent as well as a carbon source.The presence of nanosized NVPF particles in the carbon network is confirmed by field-emission scanning electron microscopy (FE-SEM) and high-resolution transmission electron microscopy (HR-TEM).The existence of carbon is analyzed by Raman scattering and elemental analysis.When applied as a Na-storage material in a potential window of 2.0-4.3 V,the electrode exhibits two flat voltage plateaus at 3.7 and 4.2 V with an electrochemically active V^3+/V^4+ redox couple.In addition,Na3V2(PO4)2F3/C composite achieved a retention capacity of ~ 88% even after 1,500 cycles at 15 C.Moreover,at high current densities of 30 and 50 C,Na3V2(PO4)2F3/C cathode retains the specific discharge capacities of 108.4 and 105.9 mAh·g-1,respectively,revealing the structural stability of the material prepared through a facile polyol refluxing method.展开更多
An easy and delicate approach using cheap carbon source as conductive materials to construct 3D sequential porous structural Na3V2(PO4)3/C(NVP/C)with high performance for cathode materials of sodium ion battery is hig...An easy and delicate approach using cheap carbon source as conductive materials to construct 3D sequential porous structural Na3V2(PO4)3/C(NVP/C)with high performance for cathode materials of sodium ion battery is highly desired.In this paper,the NVP/C with 3D sequential porous structure is constructed by a delicate approach named as“cooking porridge”including evaporation and calcination stages.Especially,during evaporation,the viscosity of NVP/C precursor is optimized by controlling the adding quantity of citric acid,thus leading to a 3D sequential porous structure with a high specific surface area.Furthermore,the NVP/C with a 3D sequential porous structure enables the electrolyte to interior easily,providing more active sites for redox reaction and shortening the diffusion path of electron and sodium ion.Therefore,benefited from its unique structure,as cathode material of sodium ion batteries,the 3D sequential porous structural NVP/C exhibits high specific capacities(115.7,88.9 and 74.4 mA·h/g at current rates of 1,20 and 50 C,respectively)and excellent cycling stability(107.5 and 80.4 mA·h/g are remained at a current density of 1 C after 500 cycles and at a current density of 20 C after 2200 cycles,respectively).展开更多
文摘通过简单的溶胶-凝胶辅助静电纺丝法得到(113)晶面优势导向的Na_3V_2(PO_4)_3/C钠离子电池正极材料,并通过对比最佳纺丝条件下分别用聚乙烯吡咯烷酮(PVP)和聚氧化乙烯(PEO)作为晶面导向剂制备的两种Na_3V_2(PO_4)_3电极材料的电化学性能,证明静电纺丝有利于实现Na_3V_2(PO_4)_3(113)晶面择优取向。在相同的电流密度(0.1 C)下,NVP-PVP和NVP-PEO的首周放电比容量分别为112.5 m A·h/g和96.3 m A·h/g,电池循环50周后,NVP-PVP仍然有98.1 m A·h/g的可逆容量保持,NVP-PEO仅仅只剩下34 m A·h/g的可逆容量保持,而即使循环100周后,NVP-PVP的可逆容量仍然在88.2 m A·h/g。结果表明,PVP静电纺丝有利于构建特定的纳米纤维结构和均一的导电碳网络骨架,进而提升主体材料Na_3V_2(PO_4)_3的电化学性能。
基金financial support from the National Natural Science Foundation of China (No.21501171,51403209,21406221,51177156/E0712)
文摘Sodium-ion batteries （SIBs） have attracted increasing attention in the past decades, because of high over-all abundance of precursors, their even geographical distribution, and low cost. Na3V2（PO4）3 （NVP）, atypical sodium super ion conductor （NASlCON）-based electrode material, exhibits pronounced structuralstability, exceptionally high ion conductivity, rendering it a most promising electrode for sodium storage.However. the comparatively low electronic conductivity makes the theoretical capacity of NVP cannot befully accessible even at comparatively low rates, presenting a major drawback for further practical ap-plications, especially when high rate capability is especially important. Thus, many endeavors have beenconformed to increase the surface and intrinsic electrical conductivity of NVP by coating the active mate-rials with a conductive carbon layer, downsizing the NVP particles, combining the NVP particle with vari-ous carbon materials and ion doping strategy. In this review, to get a better understanding on the sodiumstorage in NVP, we firstly present 4 distinct crystal structures in the temperature range of-30℃-225℃ namely α-NVP, β-NVP, β′-NVP and γ-NVP. Moreover, we give an overview of recent approaches to en-hance the surface electrical conductivity and intrinsic electrical conductivity of NVP. Finally, some poten-tial applications of NVP such as in all-climate environment and PHEV, EV fields have been prospected.
基金financially supported by"135"Projects Fund of CAS-QIBEBT Director Innovation Foundationthe Strategic Priority Research Program of the Chinese Academy of Sciences(Grant no.XDA09010105)+4 种基金the National Natural Science Foundation of China(Grant no.51502319)the Think-Tank Mutual Fund of Qingdao Energy Storage Industry Scientific Researchthe Qingdao Science and Technology Program(17-1-1-26-jch)the Youth Innovation Promotion Association CAS(No.2017253)Qingdao Key Lab of Solar Energy Utilization&Energy Storage Technology
文摘NASICON (Na-super-ionic-conductors)-structured materials have attracted extensive research interest due to their great application potential in secondary batteries. However, the mechanism of capacity fading for NASICON-structured electrode materials has been rarely studied. In this paper, we synthesized the NASICON-structured Na3V2(PO4)3/C composite by simple sol-gel and high-temperature solid-phase method and investigated its electrochemical performance in Na-Zn hybrid aqueous rechargeable batteries. After characterizing the structure, morphology and composition variations as well as the interfacial resistance changes of Na3V2(PO4)3/C cathode during cycling, we propose a mechanical and interfacial degradation mechanism for capacity fading of NASICON-structured Na3V2(PO4)3/C in Na-Zn hybrid aqueous rechargeable batteries. This work will shed light on enhancing the mechanical and in terfacial stability of NASICON-structured Na3V2(PO4)3/C in Na-Zn hybrid aqueous rechargeable batteries.
基金supported financially by the National Natural Science Foundation of China (Nos. 51672139, 51472127 and 51272144)the Projects Supported by the Key Laboratory of Pulp and Paper Science and Technology of Ministry of Education (No. KF2016-01)
文摘The rational assembly of quantum dots on two-dimensional(2 D) carbonaceous materials is very promising to produce materials, but remains a challenge. Here, we develop an assembly strategy of growing Na3 V2(PO4)3 quantum dots with superlattice structure(NVP-QDs-SL) for obtaining precise control of the size, distribution and crystallinity. The multifunctional lignocelluloses(LCs) used as a hard carbon source induce heterogeneous nucleation and confined growth of NVP-QDs-SL, leading to the uniform distribution of NVP-QDs-SL in H/S-doped hard carbon ultra-thin nanosheets(HCS). Detailed electrochemical analysis results from sodium-ion batteries of NVP-QDs-SL show that NVP-QDs-SL could trap the electrons inside HCS, significantly enhancing Na ion storage and transfer kinetics. Compared to the common Na3 V2(PO4)3 nanoparticle cathode, the NVP-QDs-SL/HCS cathode exhibits a high reversible capacity of 149.2 m A h g^-1 at a 0.1 C rate, which is far beyond the theoretical capacity of Na3 V2(PO4)3(117.6 m A h g^-1).At the ultrahigh current rate of 100 C, this cathode still remains a high discharge capacity of 40 m A h g-1.Even after cycling at 20 C over 3000 cycles, an ultrahigh coulombic efficiency close to 100% is still obtained,highlighting its excellent long cycling life, remarkable rate performance and energy density.
文摘Na_(3)V_(2)(PO_(4))_(3)(NVP)cathode material of the sodium ion battery(1 C=117 mAh g-1)has a NASICON-type structure,which not only facilitates the rapid migration of sodium ions,but also has a small volume deformation during sodium ion de-intercalation and the main frame mechanism remains unchanged,and thus is seen as an energy storage material for a wide range of applications,but has a limited electronic conductivity due to its structure.In this paper,NVP cathode materials with finer primary particles are successfully prepared using a simple hydrothermal treatment-assisted sol-gel method.The increased pore size of the NVP materials prepared under the hydrothermal process allows for more active sites and more effective resistance to the volume deformation of sodium ions during insertion/extraction processes,effectively facilitating the diffusion of ions and electrons.The Na_(3)V_(2)(PO_(4))_(3) material obtained by the optimized process exhibited good crystallinity in XRD characterization,as well as superior electrochemical properties in a series of electrochemical tests.A specific capacitance of 106.3 mAh g^(-1) at 0.2 C is demonstrated,compared to 96.5 mAh g^(-1) for Na_(3)V_(2)(PO_(4))_(3) without hydrothermal treatment,and cycling performance is also improved with 93%capacity retention.The calculated sodium ion diffusion coefficient(DNa=5.68×10^(-14))obtained after EIS curve fitting of the improved sample illustrates that the pore structure is beneficial to the performance of the Na_(3)V_(2)(PO_(4))_(3)cathode material.
基金supported by the National Natural Science Foundation of China(61071040)Leading Academic Discipline Project of Shanghai Municipal Education Commission,China(J50102)Research and Innovation Project of Shanghai Municipal Education Commission,China~~
文摘采用溶胶凝胶-高温固相法,用不同的钠源制备NASICON结构钠离子电池正极材料Na_3V_2(PO_4)_3.借助扫描电子显微镜(SEM),X射线衍射分析(XRD),电池测试系统及电化学工作站对制备的Na_3V_2(PO_4)_3结构,形貌,电性能和内阻进行表征.研究结果表明,以Na_2CO_3为钠源合成Na_3V_2(PO_4)_3有更好的颗粒尺寸,形貌结构完整,充放电性能及循环稳定性更好,阻抗也较小;在2.5~4.0 V电压范围内,以0.2C进行充放电,首次放电比容量达到110.8 m Ah/g,50次循环后容量保持率为85.1%.
基金supported by the National Natural Science Foundation of China(91963118)the Fundamental Research Funds for the Central Universities(2412019ZD010).
文摘One main challenge for phosphate cathodes in sodium-ion batteries(SIBs)is to increase the working voltage and energy density to promote its practicability.Herein,an advanced Na3V2(PO4)2F3@C cathode is prepared successfully for sodium-ion full cells.It is revealed that,carbon coating can not only enhance the electronic conductivity and electrode kinetics of Na3V2(PO4)2F3@C and inhibit the growth of particles(i.e.,shorten the Na^+-migration path),but also unexpectedly for the first time adjust the dis-/charging plateaux at different voltage ranges to increase the mean voltage(from 3.59 to 3.71 V)and energy density from 336.0 to 428.5 Wh kg^-1 of phosphate cathode material.As a result,when used as cathode for SIBs,the prepared Na3V2(PO4)2F3@C delivers much improved electrochemical properties in terms of larger specifc capacity(115.9 vs.93.5 mAh g^-1),more outstanding high-rate capability(e.g.,87.3 vs.60.5 mAh g^-1 at 10 C),higher energy density,and better cycling performance,compared to pristine Na3V2(PO4)2F3.Reasons for the enhanced electrochemical properties include ionicity enhancement of lattice induced by carbon coating,improved electrode kinetics and electronic conductivity,and high stability of lattice,which is elucidated clearly through the contrastive characterization and electrochemical studies.Moreover,excellent energy-storage performance in sodium-ion full cells further demonstrate the extremely high possibility of Na3V2(PO4)2F3@C cathode for practical applications.
文摘Na superionic conductor (NASICON)-type Na3V2(PO4)3 (NVP) has been regarded as a promising cathode material for sodium-ion batteries (SIBs). However, NVP suffers from poor cyclability and rate capability because of its intrinsically low electronic conductivity. Herein, we successfully syn thesized N-doped carb on-wrapped Na3V2(PO4)3 (NC@NVP) through the carb on izati on of polydopami ne, which is rich in nitrogen species. The strong adhesion properties of the polydopamine lead to effective and homogeneous wrapping of NVP particles, and it I is further turned into a con ductive N-doped carb on n etwork itself, providi ng facile diffusi on of electr ons and Na+ i ons duri ng battery operation. NC@NVP displays remarkable electrochemical performanee, even under harsh operating conditions, such as a high rate capability (discharge capacity of 70.88, 49.21 mA·h·g^-1 at 50 and 100 C), long-term cycling stability (capacity retention of 94.77% over 1,000 cycles at 20 C), and high-temperature cycling (capacity retention of 92.0% after 500 cycles at 60 ℃).
文摘In this study,a pseudo-layered Na super-ionic conductor of Na3V2(PO4)2F3 (NVPF)/C cathode for sodium-ion batteries is prepared successfully using a facile polyol refluxing process without any impurity phases.The X-ray diffraction and Rietveld refinement results confirm that NVPF possesses tetragonal NASICON-type lattice with a space group of P42/mnm.In this preparative method,polyol is utilized as a solvent as well as a carbon source.The presence of nanosized NVPF particles in the carbon network is confirmed by field-emission scanning electron microscopy (FE-SEM) and high-resolution transmission electron microscopy (HR-TEM).The existence of carbon is analyzed by Raman scattering and elemental analysis.When applied as a Na-storage material in a potential window of 2.0-4.3 V,the electrode exhibits two flat voltage plateaus at 3.7 and 4.2 V with an electrochemically active V^3+/V^4+ redox couple.In addition,Na3V2(PO4)2F3/C composite achieved a retention capacity of ~ 88% even after 1,500 cycles at 15 C.Moreover,at high current densities of 30 and 50 C,Na3V2(PO4)2F3/C cathode retains the specific discharge capacities of 108.4 and 105.9 mAh·g-1,respectively,revealing the structural stability of the material prepared through a facile polyol refluxing method.
基金This work was supported by the National Natural Science Foundation of China(Nos.51772294,51972306)the Natural Science Foundation of Hebei Province,China(No.B2019204009)the Youth Innovation Promotion Association of the Chinese Academy of Sciences(No.2017070).
文摘An easy and delicate approach using cheap carbon source as conductive materials to construct 3D sequential porous structural Na3V2(PO4)3/C(NVP/C)with high performance for cathode materials of sodium ion battery is highly desired.In this paper,the NVP/C with 3D sequential porous structure is constructed by a delicate approach named as“cooking porridge”including evaporation and calcination stages.Especially,during evaporation,the viscosity of NVP/C precursor is optimized by controlling the adding quantity of citric acid,thus leading to a 3D sequential porous structure with a high specific surface area.Furthermore,the NVP/C with a 3D sequential porous structure enables the electrolyte to interior easily,providing more active sites for redox reaction and shortening the diffusion path of electron and sodium ion.Therefore,benefited from its unique structure,as cathode material of sodium ion batteries,the 3D sequential porous structural NVP/C exhibits high specific capacities(115.7,88.9 and 74.4 mA·h/g at current rates of 1,20 and 50 C,respectively)and excellent cycling stability(107.5 and 80.4 mA·h/g are remained at a current density of 1 C after 500 cycles and at a current density of 20 C after 2200 cycles,respectively).
