首页 | 本学科首页   官方微博 | 高级检索  
     

ZnSe纳米晶材料的超快吸收谱
引用本文:黄仕华,陆昉.ZnSe纳米晶材料的超快吸收谱[J].半导体学报,2006,27(4):717-720.
作者姓名:黄仕华  陆昉
作者单位:浙江师范大学物理系,金华 321004;复旦大学物理系,上海 200433
摘    要:通过改进的溶剂热方法,以KBH4作为还原剂,在三乙胺溶液介质中制备了ZnSe纳米晶材料.与ZnSe体材料相比,其纳米材料的稳态吸收边发生了蓝移,而且纳米颗粒的尺寸越小,蓝移量越大,这是由于随着尺度减少而引起的量子限制效应增强造成的.对在溶液中的ZnSe纳米颗粒的超快吸收谱的研究表明,当纳米颗粒的平均尺寸为75nm时,电子-声子散射时间为8.74ps;当平均尺寸为45nm时,散射时间为2.77ps.随着纳米颗粒尺寸的减小,载流子与颗粒表面的非弹性碰撞几率增加,从而使载流子-声子耦合的强度增强,导致载流子-声子散射时间缩短.

关 键 词:ZnSe纳米晶材料  超快吸收谱  载流子-声子散射  ZnSe  纳米晶  材料  超快吸收谱  Material  Nanocrystal  Absorption  Spectra  时间缩短  强度增强  耦合  声子散射  碰撞几率  非弹性  颗粒表面  载流子  颗粒尺寸  电子  平均尺寸  研究  溶液
文章编号:0253-4177(2006)04-0717-04
收稿时间:09 1 2005 12:00AM
修稿时间:11 15 2005 12:00AM

Ultrafast Absorption Spectra of Nanocrystal ZnSe Material
Huang Shihua and Lu Fang.Ultrafast Absorption Spectra of Nanocrystal ZnSe Material[J].Chinese Journal of Semiconductors,2006,27(4):717-720.
Authors:Huang Shihua and Lu Fang
Affiliation:Department of Physics,Zhejiang Normal University,Jinhua 321004,China;Department of Physics,Fudan University, Shanghai 200433,China
Abstract:Using a modified solvothermal method in which potassium borohydride is employed as a reducing reagent,nanocrystal ZnSe materials are prepared in a triethylamine solvent.Compared to bulk ZnSe,nanocrystal ZnSe has a blue shift in its steady absorption edge.The degree of this blue shift increases with the decrease of nanocrystal particle size,as a result of quantum confinement effects.The ultrafast absorption spectra of ZnSe nanocrystals indicate that the electron-electron scattering time is 8.74ps and 2.77ps for the average nanocrystal size of 75 and 45nm,respectively.With the decrease of the size of nanocrystal,the probability of inelastic collision among carriers and nanocrystal surface increases,resulting in the enhancement of the carrier-phonon coupling strength and the shortening of the carrier-photon scattering time.
Keywords:ZnSe nanocrystals  ultrafast absorption spectroscopy  carrier-phonon scattering
本文献已被 CNKI 维普 万方数据 等数据库收录!
点击此处可从《半导体学报》浏览原始摘要信息
点击此处可从《半导体学报》下载全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号