The remote detection of chemicals using remote Raman spectroscopy and laser-induced breakdown spectroscopy (LIBS) is highly desirable for homeland security and NASA planetary exploration programs. We recently demonstrated Raman spectra with high signal-to-noise ratio of various materials from a 430 m distance during daylight with detection times of 1–10 s, utilizing a 203 mm diameter telescopic remote Raman system and 100 mJ/pulse laser energy at 532 nm for excitation. In this research effort, we describe a simple two-components approach that helps to obtain remote Raman and LIBS spectra of targets at distance of 246 m with 3 mJ/pulse in daytime. The two components of the method are: (1) a small spectroscopy system utilizing 76 mm diameter collection optics; and (2) a small remote lens near the target. Remote Raman spectra of various chemicals are presented here with detection time of 1 s. Remote LIBS spectra of minerals using single laser pulse of 3 mJ/pulse energy from a distance of 246 m are also presented. This research work demonstrates a simple approach that significantly improves remote Raman and LIBS capabilities for long range chemical detection with compact low laser power Raman and LIBS systems.

We describe the fabrication of an underwater time-gated standoff Raman sensor, consisting of a custom Raman spectrometer, custom scanner, and commercial diode-pumped pulsed 532-nm laser all located inside pressure housing. The Raman sensor was tested in the laboratory with samples in air, a tank containing tap water and seawater, and in the coastal Hawaiian harbor. We demonstrate our new system by presenting standoff Raman spectra of some of the chemicals used in homemade explosive (HME) devices and improvised explosive devices (IED), including sulfur, nitrates, chlorates, and perchlorates up to a distance of ~6 m in seawater and tap water. Finally, the Raman spectra of these hazardous chemicals sealed inside plastic containers submersed in the Hawaiian Harbor water are also presented

The recent commissioning of a movable monochromator at the 34-ID-C endstation of the Advanced Photon Source has vastly simplified the collection of Bragg coherent diffraction imaging (BCDI) data from multiple Bragg peaks of sub-micrometre scale samples. Laue patterns arising from the scattering of a polychromatic beam by arbitrarily oriented nanocrystals permit their crystal orientations to be computed, which are then used for locating and collecting several non-co-linear Bragg reflections. The volumetric six-component strain tensor is then constructed by combining the projected displacement fields that are imaged using each of the measured reflections via iterative phase retrieval algorithms. Complications arise when the sample is heterogeneous in composition and/or when multiple grains of a given lattice structure are simultaneously illuminated by the polychromatic beam. Here, a workflow is established for orienting and mapping nanocrystals on a substrate of a different material using scanning Laue diffraction microscopy. The capabilities of the developed algorithms and procedures with both synthetic and experimental data are demonstrated. The robustness is verified by comparing experimental texture maps obtained with Laue diffraction microscopy at the beamline with maps obtained from electron back-scattering diffraction measurements on the same patch of gold nanocrystals. Such tools provide reliable indexing for both isolated and densely distributed nanocrystals, which are challenging to image in three dimensions with other techniques.