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S. M. Gruner

Publications and source records attributed to S. M. Gruner.

7 recordsLinked to original sources

Photoinduced twist and untwist of moiré superlattices in TMDC heterobilayers

Two-dimensional moiré materials are formed by artificially stacking atomically thin monolayers. A wealth of correlated and topological quantum phases can be engineered via precise choice of stacking geometry. These designer electronic properties depend crucially on interlayer coupling and atomic registry. An important open question is how atomic registry responds on ultrafast timescales to optical excitation and whether the moiré geometry can be dynamically reconfigured to tune emergent phenomena in real time. Here we show that femtosecond photoexcitation drives a coherent twist-untwist motion of the moiré superlattice in $2^\circ$ and $57^\circ$ twisted WSe$_2$/MoSe$_2$ heterobilayers, resolved directly by ultrafast electron diffraction. Upon above-band-gap photoexcitation, the moiré superlattice diffraction features are enhanced within 1 ps and subsequently suppressed several picoseconds after, deviating markedly from typical photoinduced lattice heating. Kinetic diffraction analysis, supported by simulations of the sample dynamics, indicates a peak-to-trough local twist angle modulation of $0.6^\circ$, correlated with a sub-THz frequency moiré phonon. This motion is driven by ultrafast charge transfer that transiently increases interlayer attraction. Our results could lead to ultrafast control of moiré periodic lattice distortions and, by extension, the local moiré potential that shapes excitons, polarons, and correlation-driven behaviors

cond-mat.mtrl-sci

Multi-scale time-resolved electron diffraction: A case study in moiré materials

Ultrafast-optical-pump -- structural-probe measurements, including ultrafast electron and x-ray scattering, provide direct experimental access to the fundamental timescales of atomic motion, and are thus foundational techniques for studying matter out of equilibrium. High-performance detectors are needed in scattering experiments to obtain maximum scientific value from every probe particle. We deploy a hybrid pixel array direct electron detector to perform ultrafast electron diffraction experiments on a WSe$_2$/MoSe$_2$ 2D heterobilayer, resolving the weak features of diffuse scattering and moiré superlattice structure without saturating the zero order peak. Enabled by the detector's high frame rate, we show that a chopping technique provides diffraction difference images with signal-to-noise at the shot noise limit. Finally, we demonstrate that a fast detector frame rate coupled with a high repetition rate probe can provide continuous time resolution from femtoseconds to seconds, enabling us to perform a scanning ultrafast electron diffraction experiment that maps thermal transport in WSe$_2$/MoSe$_2$ and resolves distinct diffusion mechanisms in space and time.

physics.ins-det

Characterization of 128x128 MM-PAD-2.1 ASIC: A Fast Framing Hard X-Ray Detector with High Dynamic Range

We characterize a new x-ray Mixed-Mode Pixel Array Detector (MM-PAD-2.1) Application Specific Integrated Circuit (ASIC). Using an integrating pixel front-end with dynamic charge removal architecture, the MM-PAD-2.1 ASIC extends the maximum measurable x-ray signal (in 20 keV photon units) to > 10$^{7}$ x-rays/pixel/frame while maintaining a low read noise across the full dynamic range, all while imaging continuously at a frame rate of up to 10 kHz. The in-pixel dynamic charge removal mechanism prevents saturation of the input amplifier and proceeds in parallel with signal integration to achieve deadtime-less measurements with incident x-ray rates of > 10$^{10}$ x-rays/pixel/s. The ASIC format consists of 128$\times$128 square pixels each 150 $μ$m on a side and is designed to be 3-side buttable so large arrays can be effectively tiled. Here we use both laboratory x-ray sources and the Cornell High Energy Synchrotron Source (CHESS) to characterize two single ASIC prototype detectors for both low (single x-ray) and high incident flux detection. In the first detector the ASIC was solder bump-bonded to a 500 $μ$m thick Si sensor for efficient detection of x-rays below ~20 keV, whereas the second detector used a 750 $μ$m thick CdTe sensor for x-rays above $\sim$ 20 keV.

physics.ins-det

Characterization of an architecture for front-end pixel binning in an integrating pixel array detector

Optimization of an area detector involves compromises between various parameters like frame rate, read noise, dynamic range and pixel size. We have implemented and tested a novel front-end binning design in a photon-integrating hybrid pixel array detector using the MM-PAD-2.0 pixel architecture. In this architecture, the pixels can be optionally binned in a 2$\times$2 pixel configuration using a network of switches to selectively direct the output of 4 sensor pixels to a single amplifier input. Doing this allows a trade-off between frame rate and spatial resolution. Tests show that the binned pixels perform well, but with some degradation on performance as compared to an un-binned pixel. The increased parasitic input capacitance does reduce the signal collected per x-ray as well as increases the noise of the pixel. The increase in noise is, however, less than the factor of 2 increase one would observe for binning in post-processing. Spatial scans across the binned pixels show that no measured signal intensity is lost at the inner binning unit boundaries. In the high flux regime, at a 2$\times$2 pixel wide beam spot (FWHM) size, binned mode responds linearly up to a photon flux of ~10$^{7}$ x-rays/s, and performs comparably with un-binned mode up to a photon flux of ~10$^{8}$ x-rays/s. While this study demonstrates a proof of concept for front-end binning in integrating detectors, we also identify changes to this early-stage prototype which can further improve the performance of binning pixel structures.

physics.ins-det

Experimental 3D Coherent Diffractive Imaging from photon-sparse random projections

The routine atomic-resolution structure determination of single particles is expected to have profound implications for probing the structure-function relationship in systems ranging from energy materials to biological molecules. Extremely-bright, ultrashort-pulse X-ray sources---X-ray Free Electron Lasers (XFELs)---provide X-rays that can be used to probe ensembles of nearly identical nano-scale particles. When combined with coherent diffractive imaging, these objects can be imaged; however, as the resolution of the images approaches the atomic scale, the measured data are increasingly difficult to obtain and, during an X-ray pulse, the number of photons incident on the two-dimensional detector is much smaller than the number of pixels. This latter concern, the signal "sparsity," materially impedes the application of the method. We demonstrate an experimental analog using a synchrotron X-ray source that yields signal levels comparable to those expected from single biomolecules illuminated by focused XFEL pulses. The analog experiment provides an invaluable cross-check on the fidelity of the reconstructed data that is not available during XFEL experiments. We establish---using this experimental data---that a sparsity of order $1.3\times10^{-3}$ photons per pixel per frame can be overcome, lending vital insight to the solution of the atomic-resolution XFEL single particle imaging problem by experimentally demonstrating 3D coherent diffractive imaging from photon-sparse random projections.

physics.app-ph

Imaging density disturbances in water with 41.3 attosecond time resolution

We show that the momentum flexibility of inelastic x-ray scattering may be exploited to invert its loss function, alowing real time imaging of density disturbances in a medium. We show the disturbance arising from a point source in liquid water, with a resolution of 41.3 attoseconds ($4.13 \times 10^{-17}$ sec) and 1.27 $Å$ ($1.27 \times 10^{-8}$ cm). This result is used to determine the structure of the electron cloud around a photoexcited molecule in solution, as well as the wake generated in water by a 9 MeV gold ion. We draw an analogy with pump-probe techniques and suggest that energy-loss scattering may be applied more generally to the study of attosecond phenomena.

cond-mat

Pressure Induced Hydration Dynamics of Membranes

Pressure-jump initiated time-resolved x-ray diffraction studies of dynamics of the hydration of the hexagonal phase in biological membranes show that (i) the relaxation of the unit cell spacing is non-exponential in time; (ii) the Bragg peaks shift smoothly to their final positions without significant broadening or loss in crystalline order. This suggests that the hydration is not diffusion limited but occurs via a rather homogeneous swelling of the whole lattice, described by power law kinetics with an exponent $ β= 1.3 \pm 0.2$.

cond-mat