Doubling the field of view in off-axis low-coherence interferometric imaging

Pinhas Girshovitz; Natan T Shaked

doi:10.1038/lsa.2014.32

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Doubling the field of view in off-axis low-coherence interferometric imaging

Original Articles

- Doubling the field of view in off-axis low-coherence interferometric imaging
- Light: Science & Applications Vol. 3, Issue 2, (2014)
- Affiliations：
  
  Department of Biomedical Engineering, Faculty of Engineering, Tel Aviv University, Tel Aviv 69978, Israel
- Author bio：
  
  Dr NT Shaked, Department of Biomedical Engineering, Faculty of Engineering, Tel Aviv University, Ramat Aviv 69978, PO Box 39040, Tel Aviv 69978, Israel E-mail: nshaked@tau.ac.il
- Funds：
- DOI：10.1038/lsa.2014.32
  CLC：
- Published：2014-06，
  
  Published Online：14 March 2014，
  
  Received：17 June 2013，
  
  Revised：09 September 2013，
  
  Accepted：20 October 2013
- Accepted：
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Girshovitz, P. & Shaked, N. T. Doubling the field of view in off-axis low-coherence interferometric imaging. Light: Science & Applications, 3, e151 (2014).
DOI：

Girshovitz, P. & Shaked, N. T. Doubling the field of view in off-axis low-coherence interferometric imaging. Light: Science & Applications, 3, e151 (2014). DOI： 10.1038/lsa.2014.32.

摘要

Abstract

We present a new interferometric and holographic approach

named interferometry with doubled imaging area (IDIA)

with which it is possible to double the camera field of view while performing off-axis interferometric imaging

without changing the imaging parameters

such as the magnification and the resolution. This technique enables quantitative amplitude and phase imaging of wider samples without reducing the acquisition frame rate due to scanning. The method is implemented using a compact interferometric module that connects to a regular digital camera

and is useful in a wide range of applications in which neither the field of view nor the acquisition rate can be compromised. Specifically

the IDIA principle allows doubling the off-axis interferometric field of view

which might be narrower than the camera field of view due to low-coherence illumination. We demonstrate the proposed technique for scan-free quantitative optical thickness imaging of microscopic biological samples

including live neurons and a human sperm cell in rapid motion under high magnification. In addition

we used the IDIA principle to perform non-destructive profilometry during a rapid lithography process of transparent structures.

关键词

Keywords

cell imagingholographyinterferometrylithographyquantitative optical microscopy

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