4.7 Article

Combined time- and space-resolved Raman spectrometer for the non-invasive depth profiling of chemical hazards

Journal

ANALYTICAL AND BIOANALYTICAL CHEMISTRY
Volume 403, Issue 1, Pages 255-263

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00216-012-5792-2

Keywords

Time-resolved SORS; Noninvasive detection; Depth profiling; In-field screening; National security

Funding

  1. Department of the Prime Minister and Cabinet, Australian Government
  2. Queensland Government
  3. Australian Future Forensics Innovation Network (AFFIN)
  4. Queensland health forensic scientific services
  5. Australian Federal Police

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A time-resolved inverse spatially offset Raman spectrometer was constructed for depth profiling of Raman-active substances under both the lab and the field environments. The system operating principles and performance are discussed along with its advantages relative to traditional continuous wave spatially offset Raman spectrometer. The developed spectrometer uses a combination of space- and time-resolved detection in order to obtain high-quality Raman spectra from substances hidden behind coloured opaque surface layers, such as plastic and garments, with a single measurement. The time-gated spatially offset Raman spectrometer was successfully used to detect concealed explosives and drug precursors under incandescent and fluorescent background light as well as under daylight. The average screening time was 50 s per measurement. The excitation energy requirements were relatively low (20 mW) which makes the probe safe for screening hazardous substances. The unit has been designed with nanosecond laser excitation and gated detection, making it of lower cost and complexity than previous picosecond-based systems, to provide a functional platform for in-line or in-field sensing of chemical substances.

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