Imaging theory of structured pump-probe microscopy

被引:5
作者
Massaro, Eric S. [1 ]
Hill, Andrew H. [2 ]
Kennedy, Casey L. [1 ]
Grumstrup, Erik M. [1 ,2 ]
机构
[1] Montana State Univ, Dept Chem & Biochem, Bozeman, MT 59717 USA
[2] Montana State Univ, Montana Mat Sci Program, Bozeman, MT 59717 USA
关键词
ILLUMINATION MICROSCOPY; OPTICAL MICROSCOPY; DIFFRACTION-LIMIT; CARS MICROSCOPY; RESOLUTION; DYNAMICS;
D O I
10.1364/OE.24.020868
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
With sub-micron spatial resolution and femtosecond temporal resolution, pump probe microscopy provides a powerful spectroscopic probe of complex electronic environments in bulk and nanoscale materials. However, the electronic structure of many materials systems are governed by compositional and morphological heterogeneities on length scales that lie below the diffraction limit. We have recently demonstrated Structured Pump Probe Microscopy (SPPM), which employs a patterned pump excitation field to provide spectroscopic interrogation of sub-diffraction limited sample volumes. Herein, we develop the imaging theory of SPPM in two dimensions to accompany the previously published experimental methodology. We show that regardless of pump and probe wavelengths, a nearly two-fold reduction in spectroscopic probe volume can be achieved. We also examine the limitations of the approach, with a detailed discussion of ringing in the point spread function that can reduce imaging performance. (C) 2016 Optical Society of America
引用
收藏
页码:20868 / 20880
页数:13
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