No Arabic abstract
We found that temperature-dependent infrared spectroscopy measurements (i.e., reflectance or transmittance) using a Fourier-transform spectrometer can have substantial errors, especially for elevated sample temperatures and collection using an objective lens (e.g., using an infrared microscope). These errors arise as a result of partial detector saturation due to thermal emission from the measured sample reaching the detector, resulting in nonphysical apparent reduction of reflectance or transmittance with increasing sample temperature. Here, we demonstrate that these temperature-dependent errors can be corrected by implementing several levels of optical attenuation that enable convergence testing of the measured reflectance or transmittance as the thermal-emission signal is reduced, or by applying correction factors that can be inferred by looking at the spectral regions where the sample is not expected to have a substantial temperature dependence.
Thermal emission is the radiation of electromagnetic waves from hot objects. The promise of thermal-emission engineering for applications in energy harvesting, radiative cooling, and thermal camouflage has recently led to renewed research interest in this topic. There is a substantial need for accurate and precise measurement of thermal emission in a laboratory setting, which can be challenging in part due to the presence of background emission from the surrounding environment and the measurement instrument itself. This is especially true for measurements of emitters at temperatures close to that of the environment, where the impact of background emission is relatively large. In this paper, we describe, recommend, and demonstrate general procedures for thermal-emission measurements that are applicable to most experimental conditions, including less-common and more-challenging cases that include thermal emitters with temperature-dependent emissivity and emitters that are not in thermal equilibrium.
We demonstrate a high temperature performance quantum detector of Terahertz (THz) radiation based on three-dimensional metamaterial. The metamaterial unit cell consists of an inductor-capacitor (LC) resonator laterally coupled with antenna elements. The absorbing region, consisting of semiconductor quantum wells is contained in the strongly ultra-subwavelength capacitors of the LC structure. The high radiation loss of the antenna allows strongly increased collection efficiency for the incident THz radiation, while the small effective volume of the LC resonator allows intense light-matter coupling with reduced electrical area. As a result, our detectors operates at much higher temperatures than conventional quantum well detectors demonstrated so far.
Cavity ring-down spectroscopy is a ubiquitous optical method used to study light-matter interactions with high resolution, sensitivity and accuracy. However, it has never been performed with the multiplexing advantages of direct frequency comb spectroscopy without sacrificing orders of magnitude of resolution. We present dual-comb cavity ring-down spectroscopy (DC-CRDS) based on the parallel heterodyne detection of ring-down signals with a local oscillator comb to yield absorption and dispersion spectra. These spectra are obtained from widths and positions of cavity modes. We present two approaches which leverage the dynamic cavity response to coherently or randomly driven changes in the amplitude or frequency of the probe field. Both techniques yield accurate spectra of methane - an important greenhouse gas and breath biomarker. The high sensitivity and accuracy of broadband DC-CRDS, shows promise for applications like studies of the structure and dynamics of large molecules, multispecies trace gas detection and isotopic composition.
Optical spectrometers are the central instruments for exploring the interaction between light and matter. The current pursuit of the field is to design a spectrometer without the need for wavelength multiplexing optics to effectively reduce the complexity and physical size of the hardware. Based on computational spectroscopic results and combining a broadband-responsive dynamic detector, we successfully demonstrate an optics-free single-detector spectrometer that maps the tunable quantum efficiency of a superconducting nanowire into an ill-conditioned matrix to build a solvable inverse mathematical equation. Such a spectrometer can realize a broadband spectral responsivity ranging from 660 to 1900 nm. The spectral resolution at the telecom is 6 nm, exceeding the energy resolving capacity of existing infrared single-photon detectors. Meanwhile, benefiting from the optics-free setup, precise time-of-flight measurements can be simultaneously achieved. We have demonstrated a spectral LiDAR with 8 spectral channels. This work provides a concise method for building multifunctional spectrometers and paves the way for applying superconducting nanowire detectors in spectroscopy.
Optical coherence tomography (OCT) is a high-resolution three-dimensional imaging technique that enables non-destructive measurements of surface and subsurface microstructures. Recent developments of OCT operating in the mid-infrared (MIR) range (around 4 {mu}m) lifted fundamental scattering limitations and initiated applied material research in formerly inaccessible fields. The MIR spectral region, however, is also of great interest for spectroscopy and hyperspectral imaging, which allow highly selective and sensitive chemical studies of materials. In this contribution, we introduce an OCT system (dual-band, central wavelengths of 2 {mu}m m and 4 {mu}m) combined with MIR spectroscopy that is implemented as a raster scanning chemical imaging modality. The fully-integrated and cost-effective optical instrument is based on a single supercontinuum laser source (emission spectrum spanning from 1.1 {mu}m to 4.4 {mu}m). Capabilities of the in-situ correlative measurements are experimentally demonstrated by obtaining complex multidimensional material data, comprising morphological and chemical information, from a multi-layered composite ceramic-polymer specimen.