Acoustic Resonance Tuning by High-Order Lorentzian Mixing.

Nanoscale mechanical resonators have attracted a great deal of attention for signal processing, sensors, and quantum applications. Recent progress in ultrahigh-Q acoustic cavities in nanostructures allows strong interactions with various physical systems and advanced functional devices. Those acoustic cavities are highly sensitive to external perturbations, and it is hard to control those resonance properties since those responses are determined by the geometry and material. In this paper, we demonstrate a novel acoustic resonance tuning method by mixing high-order Lorentzian responses in an optomechanical system. Using weakly coupled phononic-crystal acoustic cavities, we achieve coherent mixing of second- and third-order Lorentzian responses, which is capable of the fine-tunability of the bandwidth and peak frequency of the resonance with a tuning range comparable to the acoustic dissipation rate of the device. This novel resonance tuning method can be widely applied to Lorentzian-response systems and optomechanics, especially active compensation for environmental fluctuation and fabrication errors.

Microscopic mechanisms for initiation and evolution of femtosecond laser-induced columnar structures above the surface level of aluminum.

A better understanding of the formation of femtosecond (fs) laser-induced surface structures is key to the control of their morphological profiles for desired surface functionalities on metals. In this work, with fs laser pulse irradiation, the two stages of formation mechanisms of the columnar structures (CSs) grown above the surface level are investigated on pure Al plates in ambient air. Here, we find that the redeposition of ablated microscale clusters following fs laser pulses of irradiation acts as the nucleation sites of CS formation, which strongly affects their location and density within the laser spot. Furthermore, we suggest their structural growths and morphological shape changes are directly associated with the competition among four laser-impact hydrodynamical phenomena: laser ablation, subsequent molten metal flow, particles' redeposition, and metal vapor condensation with continued pulse irradiation.

Deep learning-based optical authentication using the structural coloration of metals with femtosecond laser-induced periodic surface structures.

Structurally colored materials present potential technological applications including anticounterfeiting tags for authentication due to the ability to controllably manipulate colors through nanostructuring. Yet, no applications of deep learning algorithms, known to discover meaningful structures in data with far-reaching optimization capabilities, to such optical authentication applications involving low-spatial-frequency laser-induced periodic surface structures (LSFLs) have been demonstrated to date. In this work, by fine-tuning one of the lightweight convolutional neural networks, MobileNetV1, we investigate the optical authentication capabilities of the structurally colorized images on metal surfaces fabricated by controlling the orientation of femtosecond LSFLs. We show that the structural color variations due to a broad range of the illumination incident angles combined with both the controlled orientations of LSFLs and differences in features captured in the image make this system suitable for deep learning-based optical authentication.

Rotationally symmetric colorization of metal surfaces through omnidirectional femtosecond laser-induced periodic surface structures.

Following femtosecond (fs) laser pulse irradiation, the formation of a new type of low-spatial-frequency laser-induced periodic surface structure (LSFL) patterns, namely, omnidirectional LSFLs (OD-LSFLs) with the periodic ordering of their orientations, are investigated on Ni in this Letter. Using a liquid crystal polymer patterned depolarizer, we periodically rotate the polarization of fs laser pulses across the laser spot and create OD-LSFLs by raster scanning fs laser pulses. We also show that the period of the OD-LSFL orientation rotation can be controlled with the defocused distance, and OD-LSFLs can significantly expand the viewing angle of the structural colors in the azimuthal direction without noticeable color degradations.

Visualization of carrier dynamics in p(n)-type GaAs by scanning ultrafast electron microscopy.

Four-dimensional scanning ultrafast electron microscopy is used to investigate doping- and carrier-concentration-dependent ultrafast carrier dynamics of the in situ cleaved single-crystalline GaAs(110) substrates. We observed marked changes in the measured time-resolved secondary electrons depending on the induced alterations in the electronic structure. The enhancement of secondary electrons at positive times, when the electron pulse follows the optical pulse, is primarily due to an energy gain involving the photoexcited charge carriers that are transiently populated in the conduction band and further promoted by the electron pulse, consistent with a band structure that is dependent on chemical doping and carrier concentration. When electrons undergo sufficient energy loss on their journey to the surface, dark contrast becomes dominant in the image. At negative times, however, when the electron pulse precedes the optical pulse (electron impact), the dynamical behavior of carriers manifests itself in a dark contrast which indicates the suppression of secondary electrons upon the arrival of the optical pulse. In this case, the loss of energy of material's electrons is by collisions with the excited carriers. These results for carrier dynamics in GaAs(110) suggest strong carrier-carrier scatterings which are mirrored in the energy of material's secondary electrons during their migration to the surface. The approach presented here provides a fundamental understanding of materials probed by four-dimensional scanning ultrafast electron microscopy, and offers possibilities for use of this imaging technique in the study of ultrafast charge carrier dynamics in heterogeneously patterned micro- and nanostructured material surfaces and interfaces.

Enhanced efficiency of solar-driven thermoelectric generator with femtosecond laser-textured metals.

Through femtosecond laser irradiation, we produce in this work a unique type of surface nanostructure on Al that have enhanced absorption at UV and visible but a relatively small emissivity in infrared. By integrating this laser-treated Al to a solar-driven thermoelectric generator, we show that the thermoelectric generator integrated with the femtosecond laser-treated Al foil generates a significantly higher power than the ones without. Our study shows that our technique can dramatically enhance the efficiency of solar-driven thermoelectric devices that may lead to a leap forward in solar energy harnessing.

Femtosecond laser-induced blazed periodic grooves on metals.

In this Letter, we generate laser-induced periodic surface structures (LIPSSs) on platinum following femtosecond laser pulse irradiation. For the first time to our knowledge, we study the morphological profile of LIPSSs over a broad incident angular range, and find that the morphological profile of LIPSSs depends significantly on the incident angle of the laser beam. We show that LIPSS grooves become more asymmetric at a larger incident angle, and the morphological profile of LIPSSs formed at an incident angle over 55° eventually resembles that of a blazed grating. Our study suggests that the formation of the blazed groove structures is attributed to the selective ablation of grooves through the asymmetric periodic surface heating following femtosecond pulse irradiation. The blazed grooves are useful for controlling the diffraction efficiency of LIPSSs.

Multi-Angular Colorimetric Responses of Uni- and Omni-Directional Femtosecond Laser-Induced Periodic Surface Structures on Metals.

We investigated the colorimetric behaviors of metal surfaces with unidirectional low-spatial-frequency laser-induced periodic surface structures (UD-LSFLs) and omnidirectional LSFLs (OD-LSFLs) fabricated using femtosecond laser pulse irradiation. With the CIE standard illuminant D65, incident at -45°, we show that UD-LSFLs on metals transform polished metals to gonio-apparent materials with a unique behavior of colorimetric responses, depending on both the detection and rotation angles, whereas OD-LSFLs have nearly uniform gonio-apparent colors at each detection angle, regardless of their rotation. These colorimetric behaviors can be observed not only at the angles of diffraction but also near the angle of reflection, and we find that the power redistribution due to Rayleigh anomalies also plays an important role in the colorimetric responses of UD- and OD-LSFLs, in addition to diffraction.

Observation of dynamical crater-shaped charge distribution in the space-time imaging of monolayer graphene.

A better understanding of charge carrier dynamics in graphene is key to improvement of its electronic performance. Here, we present direct space-time visualization of carrier relaxation and diffusion in monolayer graphene using time-resolved scanning electron microscopy techniques. We observed striking fluence-dependent dynamic images, changing from a Gaussian shape to a novel crater-shaped pattern with increasing laser fluence. Such direct observation of dynamic changes in spatial charge distribution is not readily available from the conventional spectroscopic approaches, which reflect essentially overall effective carrier temperature and density. According to our analysis, for this crater-shaped carrier density to occur in aggregated electron-hole pairs in the high fluence regime there exists an unconventional Auger-assisted carrier recombination process to provide effective relaxation channels, most likely involving emission of optical phonons and plasmons, which is dynamically accessible due to a strong temporal overlap among them. The presented model allows us to successfully account for these unexpected phenomena and to quantitatively analyze the observed spatiotemporal behavior.

Development of the Triboelectric Nanogenerator Using a Metal-to-Metal Imprinting Process for Improved Electrical Output.

Triboelectric nanogenerators (TENG), which utilize contact electrification of two different material surfaces accompanied by electrical induction has been proposed and is considered as a promising energy harvester. Researchers have attempted to form desired structures on TENG surfaces and successfully demonstrated the advantageous effect of surface topography on its electrical output performance. In this study, we first propose the structured Al (SA)-assisted TENG (SA-TENG), where one of the contact layers of the TENG is composed of a structured metal surface formed by a metal-to-metal (M2M) imprinting process. The fabricated SA-TENG generates more than 200 V of open-circuit voltage and 60 µA of short-circuit current through a simple finger tapping motion. Given that the utilization of the M2M imprinting process allows for the rapid, versatile and easily accessible structuring of various metal surfaces, which can be directly used as a contact layer of the TENG to substantially enhance its electrical output performance, the present study may considerably broaden the applicability of the TENG in terms of its fabrication standpoint.

Roll-to-roll continuous patterning and transfer of graphene via dispersive adhesion.

We present a roll-to-roll, continuous patterning and transfer of graphene sheets capable of residue-free and fast patterning. The graphene sheet is supported with dispersive adhesion. Graphene is continuously patterned by the difference in adhesion forces with a pre-defined embossed roller. The patterned graphene sheet adheres to the polyethylene terephthalate (PET)/silicone with very low strength and can be easily transferred to various substrates without the aid of any heating mechanism. The width of the patterned film was 120 mm and a production rate of 15 m min(-1) for patterning was achieved. Large-area uniformity was confirmed by observing the optical images on 4 inch Si wafer and Raman mapping spectra for 50 × 50 mm(2).