无机化学学报
無機化學學報
무궤화학학보
JOURNAL OF INORGANIC CHEMISTRY
2006年
3期
477-482
,共6页
李宇展%周震%任俊霞%高学平%阎杰
李宇展%週震%任俊霞%高學平%閻傑
리우전%주진%임준하%고학평%염걸
锂离子电池%LiVPO4F%铬掺杂%循环伏安(CV)
鋰離子電池%LiVPO4F%鉻摻雜%循環伏安(CV)
리리자전지%LiVPO4F%락참잡%순배복안(CV)
lithium-ion batteries%LiVPO4F%Cr-doping%cyclic voltammetry (CV)
采用高温固相法2步合成了掺Cr的锂离子电池正极材料LiV1-xCrxPO4F(x=0,0.01,0.03,0.05,0.07),XRD测试表明LiV1-xCrxPO4F属三斜晶系.通过恒电流充放电,循环伏安和交流阻抗实验表明:掺Cr后LiVPO4F正极材料更有利于锂离子的嵌入和嵌出,材料的放电容量和循环性能进一步提高,例如,铬掺杂的LiVPO4F样品在室温、0.2 C倍率下充放电,循环50周后容量在110 mAh·g-1以上.文中还讨论了充放电容量随掺Cr量的关系,nCr含量为0.03的LiV1-xCrxPO4F有着较高的放电平台和良好的循环稳定性.
採用高溫固相法2步閤成瞭摻Cr的鋰離子電池正極材料LiV1-xCrxPO4F(x=0,0.01,0.03,0.05,0.07),XRD測試錶明LiV1-xCrxPO4F屬三斜晶繫.通過恆電流充放電,循環伏安和交流阻抗實驗錶明:摻Cr後LiVPO4F正極材料更有利于鋰離子的嵌入和嵌齣,材料的放電容量和循環性能進一步提高,例如,鉻摻雜的LiVPO4F樣品在室溫、0.2 C倍率下充放電,循環50週後容量在110 mAh·g-1以上.文中還討論瞭充放電容量隨摻Cr量的關繫,nCr含量為0.03的LiV1-xCrxPO4F有著較高的放電平檯和良好的循環穩定性.
채용고온고상법2보합성료참Cr적리리자전지정겁재료LiV1-xCrxPO4F(x=0,0.01,0.03,0.05,0.07),XRD측시표명LiV1-xCrxPO4F속삼사정계.통과항전류충방전,순배복안화교류조항실험표명:참Cr후LiVPO4F정겁재료경유리우리리자적감입화감출,재료적방전용량화순배성능진일보제고,례여,락참잡적LiVPO4F양품재실온、0.2 C배솔하충방전,순배50주후용량재110 mAh·g-1이상.문중환토론료충방전용량수참Cr량적관계,nCr함량위0.03적LiV1-xCrxPO4F유착교고적방전평태화량호적순배은정성.
A series of Cr-doped LiVPO4F cathode materials were synthesized by conventional solid-state reactions of the stoichiometric mixture of VPO4, CrPO4 and LiF, and the samples showed the same triclinic structure as the undoped LiVPO4F. The Cr-doped LiVPO4F samples were investigated on the Li extraction/insertion performances through galvanostatic charge/discharge, cyclic voltammetry (CV), and electrochemical impedance spectrum (EIS).The Cr-doped LiVPO4F systems showed improved capacity and cyclability in the voltage range of 3.0~4.6 V at different rates, for example, the measured discharge capacity of the Cr-doped LiVPO4F sample was still held over in the LiV1-xCrxPO4F samples to achieve high discharge capacity and good cyclic stability. The electrode reaction reversibility was enhanced, and the charge transfer resistance was decreased through the Cr-doping. The improved electrochemical performances of the Cr-doped LiVPO4F cathode materials are attributed to the structural stability derived from the incorporation of Cr3+ ions.