期刊文献+

不同功率激光激发下多孔硅拉曼光谱研究 被引量:1

Study on Raman Spectra of Porous Silicon with Different Excitationpower
下载PDF
导出
摘要 利用阳极氧化化学腐蚀法得到多孔硅样品,在632.8 nm激光激发下,对多孔硅的拉曼光谱随激光功率的变化进行了研究,分别得到了520 cm-1和300 cm-1附近的拉曼光谱图.发现在520 cm-1附近,激光功率较低时,多孔硅的拉曼光谱主要表现为略低于520 cm-1的尖锐单峰,随激光功率的增大,拉曼峰出现红移和不对称展宽,并且当激光功率增加到一定阈值时,单峰劈裂成双峰.而300 cm-1附近,随功率增大,峰位向低波数移动,但始终是单峰.我们对实验现象进行了分析和讨论,表明520 cm-1附近拉曼峰的红移和展宽是光学声子的量子限制效应引起的,激光功率达到一定阈值时,LO和TO声子模发生劈裂,所以单峰变为双峰.根据520 cm-1附近斯托克斯和反斯托克斯拉曼振动谱峰的强度比,我们计算了多孔硅样品表面在激光辐照下的局域的温度. Porous Silicon(PS) sample is prepared by anodization.Raman spectra of porous silicon with different laser power have been studied.Only a sharp single band near 520 cm-1 appears when the exciting laser power is low,while it shifts to the red side and shows dissymmetrical broadening with the increase of the laser power.When the laser power gets strong enough,the Raman peak near 520 cm-1 is splitted into two bands The band near 300 cm-1 also shifts to lower wavenumbers with increasing the laser power.However,no peak splitting was observed near 300 cm-1.The red-shift and dissymmetrical broadening of Raman bands can be attributed to quantum confinement effect.Double bands near 520 cm-1 at high powers are thought to be the cleavage of longitudinal optical(LO) and transverse optical(TO) modes.The local temperature of PS under the laser radiation is also calculated in the article.
机构地区 南通大学理学院
出处 《湘潭大学自然科学学报》 CAS CSCD 北大核心 2011年第2期94-98,共5页 Natural Science Journal of Xiangtan University
基金 国家自然科学基金项目(30970754) 南通大学自然科学研究项目(10Z005)
关键词 多孔硅 拉曼光谱 激光功率 porous silicon raman spectroscopy laser power
  • 相关文献

参考文献5

二级参考文献40

共引文献14

同被引文献14

  • 1贺福.用拉曼光谱研究碳纤维的结构[J].高科技纤维与应用,2005,30(6):20-25. 被引量:48
  • 2许永建,罗荣辉,郭茂田,吴俊富,李明玉.共聚焦显微拉曼光谱的应用和进展[J].激光杂志,2007,28(2):13-14. 被引量:31
  • 3Tuinstra F,Koenig J. Raman Spectrum of Graphite[J].Journal of Chemical Physics,1970.1126-1130.
  • 4AgerIiiJW,VeirsDK,ShamirJ. Laser heating effects in the characterization of carbon fibers by Raman spectroscopy[J].Journal of Applied Physics,1990,(07):3598-3608.
  • 5Huang F,Yue K T,Tan P. Temperature dependence of the Raman spectra of carbon nanotubes[J].Journal of Applied Physics,1998,(07):4022-4024.
  • 6Zickler G A,Smarsly B,GierlingerN. A reconsideration of the relationship between the crystallite size La of carbons determined by X-ray diffraction and Raman spectroscopy[J].CARBON,2006,(15):3239-3246.
  • 7Al-Jishi R,Dresselhaus G. Lattice-dynamical model for graphite[J].Physical Review B,1982.4514-4522.
  • 8Pimenta M,Dresselhaus G,Dresselhaus M S. Studying disorder in graphite-based systems by Raman spectroscopy[J].Physical Chemistry Chemical Physics,2007,(11):1276-1290.
  • 9Delhaes P,Couzi M,Trinquecoste M. A comparison between Raman spectroscopy and surface characterizations ofmultiwall carbon nanotubes[J].CARBON,2006,(14):3005-3013.
  • 10Wang A,Dhamenincourt P,Dubessy J. Characterization of graphite alteration in an uranium deposit by micro-Raman spectroscopy,X-ray diffraction,transmission electron microscopy and scanning electron microscopy[J].CARBON,1989,(02):209-218.

引证文献1

二级引证文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部