Fundamental differences between micro- and nano-Raman spectroscopy

被引:11
作者
Ayars, EJ
Jahncke, CL
Paesler, MA [1 ]
Hallen, HD
机构
[1] N Carolina State Univ, Dept Phys, Raleigh, NC 27695 USA
[2] St Lawrence Univ, Dept Phys, Canton, NY 13617 USA
来源
JOURNAL OF MICROSCOPY-OXFORD | 2001年 / 202卷
关键词
infrared spectroscopy; near-field optical microscopy; Raman spectroscopy;
D O I
10.1046/j.1365-2818.2001.00878.x
中图分类号
TH742 [显微镜];
学科分类号
摘要
Electric field polarization orientations and gradients close to near-field scanning optical microscope (NSOM) probes render nano-Raman fundamentally different from micro-Raman spectroscopy. With x-porarized light incident through an NSOM aperture, transmitted light has x, y and z components allowing nano-Raman investigators to probe a variety of polarization configurations. In addition, the strong Geld gradients in the near-field of a NSOM probe lead to a breakdown of the assumption of micro-Raman spectroscopy that the field is constant over molecular dimensions. Thus, for nano-Raman spectroscopy with an NSOM, selection rules allow for the detection of active modes with intensity dependent on the field gradient. These modes can have similar activity as infra-red absorption modes. The mechanism can also explain the origin and intensity of some Raman modes observed in surface enhanced Raman spectroscopy.
引用
收藏
页码:142 / 147
页数:6
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