Raman spectra of twisted bilayer graphene close to the magic angle

In this work, we study the Raman spectra of twisted bilayer graphene samples as a function of their twist-angles (θ), ranging from 0.03º to 3.40º, where local θ are determined by analysis of their associated moiré superlattices, as imaged by scanning microwave impedance microscopy. Three standard excitation laser lines are used (457, 532, and 633 nm wavelengths), and the main Raman active graphene bands (G and 2D) are considered. Our results reveal that electron-phonon interaction influences the G band's linewidth close to the magic angle regardless of laser excitation wavelength. Also, the 2D band lineshape in the θ < 1º regime is dictated by crystal lattice and depends on both the Bernal (AB and BA) stacking bilayer graphene and strain soliton regions (SP) [1]. We propose a geometrical model to explain the 2D lineshape variations, and from it, we estimate the SP width when moving towards the magic angle.

High sensitivity hydrogen analysis in zircaloy-4 using helium-assisted excitation laser-induced breakdown spectroscopy

High-sensitivity detection of hydrogen (H) contained in zircaloy-4, a commonly used material for nuclear fuel containers, is crucial in a nuclear power plant. Currently, H detection is performed via gas chromatography, which is an offline and destructive method. In this study, we developed a technique based on metastable excited-state He-assisted excitation to achieve excellent quality of H emission spectra in double-pulse orthogonal laser-induced breakdown spectroscopy (LIBS). The production of metastable excited-state He atoms is optimized by using LiF as sub-target material. The results show a narrow full-width-at-half-maximum of 0.5 Å for the H I 656.2 nm emission line, with a detection limit as low as 0.51 mg/kg. Thus, using this novel online method, H in zircaloy-4 can be detected efficiently, even at very low concentrations.

Microfluidic Raman Sensing Using a Single Ring Negative Curvature Hollow Core Fiber

A compact microfluidic Raman detection system based on a single-ring negative-curvature hollow-core fiber is presented. The system can be used for in-line qualitative and quantitative analysis of biochemicals. Both efficient light coupling and continuous liquid injection into the hollow-core fiber were achieved by creating a small gap between a solid-core fiber and the hollow-core fiber, which were fixed within a low-cost ceramic ferrule. A coupling efficiency of over 50% from free-space excitation laser to the hollow core fiber was obtained through a 350 μm-long solid-core fiber. For proof-of-concept demonstration of bioprocessing monitoring, a series of ethanol and glucose aqueous solutions at different concentrations were used. The limit of detection achieved for the ethanol solutions with our system was ~0.04 vol.% (0.32 g/L). Such an all-fiber microfluidic device is robust, provides Raman measurements with high repeatability and reusability, and is particularly suitable for the in-line monitoring of bioprocesses.

Detectable Depth of Copper, Steel, and Aluminum Alloy Plates with Pulse-Echo Laser Ultrasonic Propagation Imaging System

Pulse-echo laser ultrasonic propagation imaging is a nondestructive testing technique developed for composite materials and aluminum alloys used in aerospace. Although this method has been in usage for a considerable time, information of the detectable depth and the relationship between ultrasonic frequencies and the acoustic properties of metals is not readily available. Therefore, we investigate the A-scan and C-scan ultrasonic testing data of aluminum alloy, hot rolled steel, stainless steel, and copper alloy, which are used in aircraft bodies, frameworks, and gas pipelines. Experiments are performed with the pulse-width and excitation laser power fixed at 32 ns and approximately 4 W, respectively. The metal specimens include 24 artificial cylindrical defects with a diameter of 5 mm, located at depths of 1–12 mm on the front surface. The A-scan and C-scan data obtained at room temperature indicate the detectable depth for metals via the pulse-echo laser ultrasonic propagation imaging technique.

Investigation of photoluminescence kinetics CuInS2/ZnS quantum dots

The kinetics of photoluminescence of CuInS2/ZnS quantum dots at room temperature has been studied. We show that the parameters of the photoluminescence band of our quantum dots, i.e. its position and FWHM, do not depend on the delay time after the excitation laser pulse. These may suggest the spectral diffusion of photoluminescence of CuInS2/ZnS quantum dots due to hole localization at different Cu sites.

Non-Invasive Monitoring of Ethanol and Methanol Levels in Grape-Derived Pisco Distillate by Vibrational Spectroscopy

Handheld Raman and portable FT-IR spectroscopy devices were evaluated for fast and non-invasive determination of methanol and ethanol levels in Peruvian Pisco. Commercial Peruvian Pisco (n = 171) samples were kindly provided by the UNALM Alliance for Research in Alcohol and its Derivatives (Lima, Peru) and supplemented by purchases at grocery and online stores. Pisco spectra were collected on handheld Raman spectrometers equipped with either a 1064 nm or a 785 nm excitation laser and a portable infrared unit operating in transmission mode. The alcohol levels were determined by GC–MS. Calibration models used partial least-squares regression (PLSR) to develop prediction algorithms. GC–MS data revealed that 10% of Pisco samples had ethanol levels lower than 38%, indicating possible water dilution. Methanol levels ranged from 10 to 130 mg/100 mL, well below the maximum levels allowed for fruit brandies. Handheld Raman equipped with a 1064 nm excitation laser gave the best results for determining ethanol (SEP = 1.2%; RPre = 0.95) and methanol (SEP = 1.8 mg/100 mL; RPre = 0.93). Randomly selected Pisco samples were spiked with methanol (75 to 2800 mg/100 mL), and their Raman spectra were collected through their genuine commercial bottles. The prediction models gave an excellent performance (SEP = 98 mg/100 mL; RPre = 0.97), allowing for the non-destructive and non-contact determination of methanol and ethanol concentrations without opening the bottles.

Real-time RGB color-tunable upconversion luminescence using a single excitation wavelength

Real-time color-tunable upconversion luminescence of lanthanide ions has recently attracted increasing attention. To date, at least two different excitation wavelengths are required to obtain tunable upconversion colors containing the three-primary-color components (Red-Green-Blue). In this work, for the first time, we demonstrate that it is possible achieving tunable three-primary-color upconversion luminescence using a single excitation wavelength, on the basis of the photon-order dependent uponversion nature. A core-shell-shell nanocrystal was synthesized, with rational designed compositions of Er/Yb and Tm/Yb in the core and the outermost shell, respectively, responsible for the green/red and blue emissions. By increasing the power density of the 980 nm continuous-wave excitation laser, the color of the emitted luminescence of the core-shell-shell nanocrystal evolved as green → red → blue, corresponding to 2 → 3 → 4-photons involved in the upconversion process.

MEMS enabled miniaturized light-sheet microscopy with all optical control

We have designed and implemented a compact, cost-efficient miniaturised light-sheet microscopy system based on optical microelectromechanical systems scanners and tunable lenses. The system occupies a footprint of 20 × 28 × 13 cm3 and combines off-the-shelf optics and optomechanics with 3D-printed structural and optical elements, and an economically costed objective lens, excitation laser and camera. All-optical volume scanning enables imaging of 435 × 232 × 60 µm3 volumes with 0.25 vps (volumes per second) and minimum lateral and axial resolution of 1.0 µm and 3.8 µm respectively. An open-top geometry allows imaging of samples on flat bottomed holders, allowing integration with microfluidic devices, multi-well plates and slide mounted samples, with applications envisaged in biomedical research and pre-clinical settings.

Excitation Conditions for Surface-Enhanced Hyper Raman Scattering With Biocompatible Gold Nanosubstrates

Surface enhanced hyper Raman scattering (SEHRS) can provide many advantages to probing of biological samples due to unique surface sensitivity and vibrational information complementary to surface-enhanced Raman scattering (SERS). To explore the conditions for an optimum electromagnetic enhancement of SEHRS by dimers of biocompatible gold nanospheres and gold nanorods, finite-difference time-domain (FDTD) simulations were carried out for a broad range of excitation wavelengths from the visible through the short-wave infrared (SWIR). The results confirm an important contribution by the enhancement of the intensity of the laser field, due to the two-photon, non-linear excitation of the effect. For excitation laser wavelengths above 1,000 nm, the hyper Raman scattering (HRS) field determines the enhancement in SEHRS significantly, despite its linear contribution, due to resonances of the HRS light with plasmon modes of the gold nanodimers. The high robustness of the SEHRS enhancement across the SWIR wavelength range can compensate for variations in the optical properties of gold nanostructures in real biological environments.

Optical Feedback for Sensitivity Enhancement in Direct Raman Detection of Liquids

Detection of low-concentration molecules in liquids has been a challenge in sensing technologies. Raman spectroscopy is an effective approach for trace detection, which is in fact a “volume-excitation” and “volume-collection” technique in the analysis of liquid samples. However, for the commonly employed one-pass excitation and back-scattering detection scheme, a large portion of both the excitation laser energy and the Raman-scattering light energy is wasted without efficient reuse or collection. In this consideration, we demonstrate a broadband optical feedback scheme by a curved high-reflection mirror for both the excitation and the Raman-scattering light, so that the excitation and the forward-propagating Raman signal can be back-reflected and collected with a high efficiency. Using the “F+2f” design, where F and f are the focal lengths of the focusing lens and curved reflection mirror, respectively, we were able to not only produce two focuses of the excitation laser beam but also extend the Raman interaction by a doubled distance. For the detection of pure ethanol molecules and the R6G molecules in water with a concentration of 10−3 M, the Raman signal was enhanced by a factor of about 5.6. The optical feedback scheme and discovered optical mechanisms supply effective improvements to the Raman spectroscopic measurements on liquid samples.