物理化学学报
物理化學學報
물이화학학보
ACTA PHYSICO-CHIMICA SINICA
2009年
5期
1004-1008
,共5页
胡国荣%曹雁冰%彭忠东%杜柯%蒋庆来
鬍國榮%曹雁冰%彭忠東%杜柯%蔣慶來
호국영%조안빙%팽충동%두가%장경래
锂离子电池%正极材料%Li2FeSiO4%微波合成
鋰離子電池%正極材料%Li2FeSiO4%微波閤成
리리자전지%정겁재료%Li2FeSiO4%미파합성
Li-ion battery%Cathode material%Li2FeSiO4%Microwave synthesis
研究了一种制备锂离子电池正极材料Li2FeSiO4的新方法.采用机械球磨结合微波热处理合成了Li2FeSiO4正极材料.通过XRD、SEM和恒流充放电测试,对样品结构、形貌和电化学性能进行了表征和分析.与传统固相法合成的材料在晶体结构、微观形貌以及充放电性能方面进行了比较.结果表明,微波合成法可以快速制备具有正交结构的Li2FeSiO4材料;在650 ℃时处理12 min,获得了纯度高、晶粒细小均匀的产物,该产物具有较高的放电比容量和良好的循环性能.在60℃下以C/20倍率(电流密度,1C=160mA·g-1)进行充放电,首次放电容量为119.5 mAh·g-1,10次循环后放电容量为116.2 mAh·g-1.与传统高温固相法相比,微波合成法制备的材料具有较高的纯度、均匀的形貌和较好的电化学性能.
研究瞭一種製備鋰離子電池正極材料Li2FeSiO4的新方法.採用機械毬磨結閤微波熱處理閤成瞭Li2FeSiO4正極材料.通過XRD、SEM和恆流充放電測試,對樣品結構、形貌和電化學性能進行瞭錶徵和分析.與傳統固相法閤成的材料在晶體結構、微觀形貌以及充放電性能方麵進行瞭比較.結果錶明,微波閤成法可以快速製備具有正交結構的Li2FeSiO4材料;在650 ℃時處理12 min,穫得瞭純度高、晶粒細小均勻的產物,該產物具有較高的放電比容量和良好的循環性能.在60℃下以C/20倍率(電流密度,1C=160mA·g-1)進行充放電,首次放電容量為119.5 mAh·g-1,10次循環後放電容量為116.2 mAh·g-1.與傳統高溫固相法相比,微波閤成法製備的材料具有較高的純度、均勻的形貌和較好的電化學性能.
연구료일충제비리리자전지정겁재료Li2FeSiO4적신방법.채용궤계구마결합미파열처리합성료Li2FeSiO4정겁재료.통과XRD、SEM화항류충방전측시,대양품결구、형모화전화학성능진행료표정화분석.여전통고상법합성적재료재정체결구、미관형모이급충방전성능방면진행료비교.결과표명,미파합성법가이쾌속제비구유정교결구적Li2FeSiO4재료;재650 ℃시처리12 min,획득료순도고、정립세소균균적산물,해산물구유교고적방전비용량화량호적순배성능.재60℃하이C/20배솔(전류밀도,1C=160mA·g-1)진행충방전,수차방전용량위119.5 mAh·g-1,10차순배후방전용량위116.2 mAh·g-1.여전통고온고상법상비,미파합성법제비적재료구유교고적순도、균균적형모화교호적전화학성능.
We report a novel synthetic route for the preparation of the Li2FeSiO4 cathode material by microwave processing.The Li2FeSiO4 material was synthesized using mechanical ball-milling and subsequent microwave processing.The prepared samples were characterized by X-ray diffraction,manning electron microscopy,and electrochemical methods.Properties of the prepared materials and electrochemical characteristics of the samples were investigated and compared to samples prepared by the conventional solid-state reaction.The obtained results indicated that highly pure Li2FeSiO4 material with uniform and fine particle size was quickly and successfully synthesized by microwave(MW) heating at 650℃ for 12 min.This compound showed high specific capacity and good cycle ability.The initial discharge capacity of the sample obtained by MW heating delivered 119.5 mAh·g-1 at 60℃ at a current density of C/20 rate(1C=160 mA·g-1).After 10 cycles the discharge capacity maintained 116.2 mAh·g-1.The Li2FeSiO4 material displayed higher phase purity,better microstructure,and better electrochemical properties than the sample prepared by the conventional solid-state method.