ABSTRACT
Methods that allow versatile manipulation of metastable centers in semiconductors are highly important owing to their potential for quantum information processing and computations. In this study, we demonstrate that the electron-phonon interaction enables phonon participation to promote relaxation of metastable centers in ZnO, which is known for its persistent photoconductivity (PPC) effect. Experimentally, we show that continuous infrared (IR) radiation (1064 nm, â¼30 mW/cm2) promotes longitudinal optical phonons via the Fröhlich interaction and increases the PPC relaxation rate by â¼4 folds. More importantly, we discover that coherent phonons activated by an ultrashort pulse IR laser of the same power increased the relaxation rate by â¼1200-fold, as confirmed by ultrafast transient spectroscopy to be correlated to the excitation of coherent acoustic phonons via the inverse piezoelectric effect. We expect this study to provide valuable guidance for the development of novel quantum and photoactive devices.
ABSTRACT
Low-cost, high-quality, and large-area superhydrophobic surfaces are in high demand. This study demonstrates laser-engineered polydimethylsiloxane (PDMS) as a platform for versatile and highly efficient water manipulation. The fabrication process consists of two steps: patterning PDMS with arrayed microlenses and laser pulse scanning. The obtained PDMS is superhydrophobic and exhibits excellent chemical resistance, UV stability, pressure robustness, and substantial mechanical durability. Notably, there is no significant change in the water contact angles after storage in air for 14 months. Microstructural analysis revealed that the sample contained stable nanostructured inorganics such as crystalline silicon, silicon carbide, and sp3-like carbon. The superhydrophobic surface was demonstrated to have versatile and wide applications in oil/water separation and water collection.
ABSTRACT
Controlled droplet manipulation by light has tremendous technological potential. We report here a method based on photothermally induced pyroelectric effects that enables manipulation and maneuvering of a water droplet on a superhydrophobic surface fabricated on lithium tantalite (LiTaO3). In particular, we demonstrate that the pyroelectric charge distribution has an essential role in this process. Evenly distributed charges promote a rapid hydrophobic to hydrophilic transition featuring a very large water contact angle (WCA) change of â¼76.5° in air. This process becomes fully reversible in silicone oil. In contrast, the localized charge distribution induced by guided laser illumination leads to very different and versatile functionalities, including droplet shape control and motion manipulation. The influence of a saline solution is also investigated and compared to the deionized water droplet. The focusing effect of the water droplet, a phenomenon that widely exists in nature, is particularly of interest. Simple tuning of the laser incident angle results in droplet deformation, jetting, splitting, and guided motion. Potential applications, such as droplet pinning and transfer, are presented. This approach offers a wide range of versatile functionalities and ready controllability, including contactless, electrodeless, and precise spatial and fast temporal control, with tremendous potential for applications requiring remote droplet control.
ABSTRACT
The design and fabrication of surfaces that support rapid wetting transition remain technologically challenging. Here, we examine the effects of optical illumination on the wetting behaviors of zinc oxide (ZnO) single crystals. We find that ultraviolet irradiation above the band gap energy promotes a rapid wetting transition, characterized by sliding of the water droplet, within a few seconds. Notably, the transition for Zn-polar (0001) ZnO surfaces is even faster than that for O-polar (0001Ì ) ZnO surfaces. We confirmed that process is dependent on power, surface polarity, and solution pH and reversible through illumination by near-infrared light, which restores the water contact angle back to its initial value. Surface chemical analysis revealed that the instantaneous photocatalytic formation of surface-terminated hydroxyl (-OH) groups is responsible for the observed rapid wetting transition. Density functional theory calculations with the inclusion of onsite Coulomb interactions revealed that both the Zn-polar and O-polar surfaces can be easily covered with -OH groups through the adsorption of -OH groups or hydrogen atoms, respectively. This study develops a route to fabricate optically active and controllable microfluidic devices that support rapid wetting transitions for water droplet manipulation.
