Multiplex Raman induced Kerr effect microscopy

被引：17

作者：

Bachler, Brandon R. ^{[1
]}

Fermann, Martin E. ^{[2
]}

Ogilvie, Jennifer P. ^{[1
,2
]}

机构：

[1] Univ Michigan, Dept Phys & Biophys, Ann Arbor, MI 48109 USA

[2] IMRA Amer Inc, Ann Arbor, MI 48105 USA

来源：

OPTICS EXPRESS | 2012年 / 20卷 / 02期

基金：

美国国家科学基金会;

关键词：

SCATTERING MICROSCOPY; STIMULATED RAMAN; HETERODYNE-DETECTION; EFFECT SPECTROSCOPY; TRANSFORM; PULSE; POLARIZATION; SENSITIVITY; LASER; SPECTRA;

D O I：

10.1364/OE.20.000835

中图分类号：

O43 [光学];

学科分类号：

070207 [光学];

摘要：

We report spectrally-resolved chemical imaging based on Raman induced Kerr effect spectroscopy (RIKES). When used with circularly-polarized pump excitation, multiplex RIKES offers the potential for spectrally-resolved imaging free of the nonresonant background that plagues coherent anti-Stokes Raman scattering. RIKES does however have a highly sample-dependent birefringent background that limits its sensitivity and can introduce spectral distortions. We demonstrate that in low birefringence samples multiplex RIKES microscopy offers an enhanced signal-to-noise ratio compared to multiplex stimulated Raman scattering (SRS) when implemented in a high polarization-purity, low frequency chopping scheme. (C)2012 Optical Society of America

引用

页码：835 / 844

页数：10

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