Spatial Heterodyne Offset Raman Spectroscopy Enabling Rapid, High Sensitivity Characterization of Materials’ Interfaces
Source abstract
Abstract
Abstract Spatially offset Raman spectroscopy is integrated with a fiber‐coupled spatial heterodyne spectrometer to collect Raman spectra from deep within opaque or scattering materials. The method, named spatial heterodyne offset Raman spectroscopy generates a wavenumber‐dependent spatial phase shift of the optical signal as a “spectral” image on a charge‐coupled device detector. The image can be readily processed from the spatial domain using a single, simple, and “on‐the‐fly” Fourier transform to generate Raman spectra, in the frequency domain. By collecting all of the spatially offset Raman scattered photons that pass through the microscope's collection objective lens, the methodology gives an improvement in the Raman sensitivity by an order of magnitude. The instrumentation is both mechanically robust and “movement‐free,” which when coupled with the associated advantages of highly efficient signal collection and ease of data processing, enables rapid interfacial analysis of complex constructs based on established biomaterials models.
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Research context
OpenAlex topics: Spectroscopy Techniques in Biomedical and Chemical Research · Photoacoustic and Ultrasonic Imaging · Optical Coherence Tomography Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Beijing Key Lab for Precision Optoelectronic Measurement Instrument and Technology School of Optics and Photonics Beijing Institute of Technology Beijing 100081 China
Division of Biomedical Engineering James Watt School of Engineering University of Glasgow Glasgow G12 8LT UK
Funding
Engineering and Physical Sciences Research Council
References (39)
Show source-provided references
1. 10.1038/121501c010.1038/121501c0 ↗
2. 10.1586/17434440.3.2.21510.1586/17434440.3.2.215 ↗
3. 10.1021/acs.analchem.5b0253710.1021/acs.analchem.5b02537 ↗
4. 10.1098/rsif.2013.046410.1098/rsif.2013.0464 ↗
5. 10.1038/s41536-018-0042-710.1038/s41536-018-0042-7 ↗
6. 10.1080/05704928.2013.86320510.1080/05704928.2013.863205 ↗
7. 10.1366/000370205364145010.1366/0003702053641450 ↗
8. 10.1002/jbio.20120014110.1002/jbio.201200141 ↗
9. 10.1039/C7AN00894E10.1039/C7AN00894E ↗
10. 10.1039/C6AY02327D10.1039/C6AY02327D ↗
11. 10.1021/acs.analchem.9b0101510.1021/acs.analchem.9b01015 ↗
12. 10.1366/00037020677602334010.1366/000370206776023340 ↗
13. 10.1366/00037020677899910210.1366/000370206778999102 ↗
14. 10.1002/jbio.20170012910.1002/jbio.201700129 ↗
15. 10.1109/ACCESS.2020.298417010.1109/ACCESS.2020.2984170 ↗
16. Harlander J. M. · 1990
17. J. M.Harlander PhD Thesis The University of Wisconsin‐Madison 1991.
18. 10.1364/OE.25.00159810.1364/OE.25.001598 ↗
19. 10.1086/17175610.1086/171756 ↗
20. 10.1002/jrs.512110.1002/jrs.5121 ↗
21. 10.1177/000370281663130410.1177/0003702816631304 ↗
22. 10.1002/jrs.578810.1002/jrs.5788 ↗
23. 10.1177/000370281771945310.1177/0003702817719453 ↗
24. 10.1364/OE.23.00302710.1364/OE.23.003027 ↗
25. 10.1177/000370281666512710.1177/0003702816665127 ↗
26. 10.1177/000370282090622210.1177/0003702820906222 ↗
27. 10.1364/OE.26.01199410.1364/OE.26.011994 ↗
28. 10.1364/OE.24.01270110.1364/OE.24.012701 ↗
29. 10.1177/000370282095731110.1177/0003702820957311 ↗
30. 10.1039/C4AN01889C10.1039/C4AN01889C ↗
31. 10.1016/j.molstruc.2010.03.05410.1016/j.molstruc.2010.03.054 ↗
32. 10.1021/acscentsci.6b0022210.1021/acscentsci.6b00222 ↗
33. 10.1016/j.bone.2006.06.00810.1016/j.bone.2006.06.008 ↗
34. 10.1002/jrs.188410.1002/jrs.1884 ↗
35. 10.1117/1.336900310.1117/1.3369003 ↗
36. 10.1088/1674-1056/17/10/03010.1088/1674-1056/17/10/030 ↗
37. 10.1007/978-90-481-8831-4_810.1007/978-90-481-8831-4_8 ↗
38. 10.1007/s11999-010-1692-y10.1007/s11999-010-1692-y ↗
39. 10.1117/1.42999410.1117/1.429994 ↗