We used nonlinear laser scanning optical microscopy to study atomically thin transition metal dichalcogenides (TMDs) and revealed, with unprecedented resolution, the orientational distribution of armchair directions and their degree of organization in the two-dimensional (2D) crystal lattice. In particular, we carried out polarization-resolved second-harmonic generation (PSHG) imaging for monolayer WS2 and obtained, with high-precision, the orientation of the main crystallographic axis (armchair orientation) for each individual 120 × 120 nm2 pixel of the 2D crystal area. Such nanoscale resolution was realized by fitting the experimental PSHG images, obtained with sub-micron precision, to a new generalized theoretical model that accounts for the nonlinear optical properties of TMDs. This enabled us to distinguish between different crystallographic domains, locate boundaries and reveal fine structure. As a consequence, we can calculate the mean orientational average of armchair angle distributions in specific regions of interest and define the corresponding standard deviation as a figure-of-merit for the 2D crystal quality.

Stacked atomically thin transition metal dichalcogenides (TMDs) exhibit fundamentally new physical properties compared to those of the individual layers. The twist angle between the layers plays a crucial role in tuning these properties. Having a tool that provides high-resolution, large area mapping of the twist angle, would be of great importance in the characterization of such 2D structures. Here we use polarization-resolved second harmonic generation (P-SHG) imaging microscopy to rapidly map the twist angle in large areas of overlapping WS2 stacked layers. The robustness of our methodology lies in the combination of both intensity and polarization measurements of SHG in the overlapping region. This allows the accurate measurement and consequent pixel-by-pixel mapping of the twist angle in this area. For the specific case of 30° twist angle, P-SHG enables imaging of individual layers.

We use laser-scanning nonlinear imaging microscopy in atomically thin transition metal dichalcogenides (TMDs) to reveal information on the crystalline orientation distribution, within the 2D lattice. In particular, we perform polarization-resolved second-harmonic generation (PSHG) imaging in a stationary, raster-scanned chemical vapor deposition (CVD)-grown WS 2 flake, in order to obtain with high precision a spatially resolved map of the orientation of its main crystallographic axis (armchair orientation). By fitting the experimental PSHG images of sub-micron resolution into a generalized nonlinear model, we are able to determine the armchair orientation for every pixel of the image of the 2D material, with further improved resolution. This pixel-wise mapping of the armchair orientation of 2D WS 2 allows us to distinguish between different domains, reveal fine structure, and estimate the crystal orientation variability, which can be used as a unique crystal quality marker over large areas. The necessity and superiority of a polarization-resolved analysis over intensity-only measurements is experimentally demonstrated, while the advantages of PSHG over other techniques are analysed and discussed.

Elemental analysis of biogeochemical archives is an established technique used to study climate in a range of applications, including ocean circulation, glacial/interglacial climates, and anthropogenic climate change. Data from mollusc archives are especially important because of their global abundance and sub-annual resolution. Despite this potential, they are underrepresented among palaeoclimate studies, due to enigmatic physiological influences skewing the elemental record. Understanding the patterns behind these influences will improve data interpretation and lead to the development of new climate proxies. Here, we show for the first time that extensive spatial mapping of multiple mollusc specimens using Laser Induced Breakdown Spectroscopy (LIBS) across a wider region can resolve enigmatic patterns within the elemental record caused by physiological influences. 2D elemental (Mg/Ca) maps of whole limpet shells (Patella caerulea) from across the Mediterranean revealed patterns of variability within individual mollusc records as well as within isochronous parts of specimens. By registering and quantifying these patterns, we established previously uninterpretable correlations with temperature (R 2 > 0.8, p < 0.01). This outcome redefines the possibilities of accessing sub-annual climate proxies and presents the means to assess annual temperature ranges using oxygen isotope analysis requiring only 2 samples per shell.

Degenerate minima in momentum space—valleys—provide an additional degree of freedom that can be used for information transport and storage. Notably, such minima naturally exist in the band structure of transition metal dichalcogenides (TMDs). When these atomically thin crystals interact with intense laser light, the second harmonic generated (SHG) field inherits special characteristics that reflect not only the broken inversion symmetry in real space but also the valley anisotropy in reciprocal space. The latter is present whenever there exists a valley population imbalance (VPI) between the two valleys and affects the polarization state of the detected SHG. In this work, it is shown that the temperature-induced change of the SHG intensity dependence on the excitation field polarization is a fingerprint of VPI in TMDs. In particular, pixel-by-pixel VPI mapping based on polarization-resolved raster-scanning imaging microscopy was performed inside a cryostat to generate the SHG contrast in the presence of VPI from every point of a TMD flake. The generated contrast is marked by rotation of the SHG intensity polar diagrams at low temperatures and is attributed to the VPI-induced SHG.

Here we apply Laser Induced Breakdown Spectroscopy (LIBS) to efficiently map the elemental change throughout the growth increments of three mollusc shells. We employ an automated LIBS setup to map the Mg/Ca composition of whole shell sections with over 2000 data points per hour.

Two-dimensional (2D) transition metal dichalcogenides (TMDs) offer unique optoelectronic capabilities due to their direct bandgap semiconductor nature in monolayer form. Atomically thin TMDs can be assembled in vertical stacks that are held together by van der Waals forces, enabling interlayer coupling between the layers. This creates new physical properties that depend on the relative orientation (twist angle) between the TMD monolayers. Accurate and fast measurement of the twist angle is therefore of utmost importance for characterizing a 2D TMD heterostructure. Here, we present a nonlinear imaging technique based on second harmonic generation (SHG) microscopy, that enables instantaneous mapping of the twist angle between the two stacked TMD monolayers. By using a polarization beam splitter in the detection path and two detectors measuring two orthogonal SHG polarization components, we acquire with a single-shot measurement the twist angle in a WS2/MoS2 heterobilayer, in real time. Remarkably, the twist angle is measured directly in the overlapping region based on a SHG interference model. The demonstrated technique offers a powerful tool for the rapid, all-optical and spatially resolved twist angle determination in large-area 2D TMD heterostructures.

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