White-light diffraction phase microscopy at doubled space-bandwidth product

被引:3
|
作者
Shan, Mingguang [1 ,2 ]
Kandel, Mikhail E. [1 ]
Majeed, Hassaan [1 ]
Nastasa, Viorel [1 ,3 ]
Popescu, Gabriel [1 ]
机构
[1] Univ Illinois, Dept Elect & Comp Engn, Beckman Inst Adv Sci & Technol, Quantitat Light Imaging Lab, Urbana, IL 61801 USA
[2] Harbin Engn Univ, Coll Informat & Commun Engn, Harbin 150001, Heilongjiang, Peoples R China
[3] Natl Inst Laser Plasma & Radiat Phys, Magurele 077125, Ilfov, Romania
来源
OPTICS EXPRESS | 2016年 / 24卷 / 25期
基金
美国国家科学基金会; 中国国家自然科学基金;
关键词
DIGITAL HOLOGRAPHIC MICROSCOPY; REFRACTIVE-INDEX; DYNAMICS; CELLS; BLOOD; ILLUMINATION;
D O I
10.1364/OE.24.029039
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
White light diffraction microscopy (wDPM) is a quantitative phase imaging method that benefits from both temporal and spatial phase sensitivity, granted, respectively, by the common-path geometry and white light illumination. However, like all off-axis quantitative phase imaging methods, wDPM is characterized by a reduced space-bandwidth product compared to phase shifting approaches. This happens essentially because the ultimate resolution of the image is governed by the period of the interferogram and not just the diffraction limit. As a result, off-axis techniques generates single-shot, i. e., high timebandwidth, phase measurements, at the expense of either spatial resolution or field of view. Here, we show that combining phase-shifting and off-axis, the original space-bandwidth is preserved. Specifically, we developed phase-shifting diffraction phase microscopy with white light, in which we measure and combine two phase shifted interferograms. Due to the white light illumination, the phase images are characterized by low spatial noise, i. e., < 1nm pathlength. We illustrate the operation of the instrument with test samples, blood cells, and unlabeled prostate tissue biopsy. (C) 2016 Optical Society of America
引用
收藏
页码:29034 / 29040
页数:7
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