RESUMEN
Structural coloring is a photostable and environmentally friendly coloring approach that harnesses optical interference and nanophotonic resonances to obtain colors with a range of applications including display technologies, colorful solar panels, steganography, décor, data storage, and anticounterfeiting measures. We show that optical coatings exhibiting the photonic Fano Resonance present an ideal platform for structural coloring; they provide full color access, high color purity, high brightness, controlled iridescence, and scalable manufacturing. We show that an additional oxide film deposited on Fano resonant optical coatings (FROCs) increases the color purity (up to 99%) and color gamut coverage range of FROCs to 61% of the CIE color space. For wide-area structural coloring applications, FROCs have a significant advantage over existing structural coloring schemes.
RESUMEN
In this work, we report on the creation of a black copper via femtosecond laser processing and its application as a novel electrode material. We show that the black copper exhibits an excellent electrocatalytic activity for hydrogen evolution reaction (HER) in alkaline solution. The laser processing results in a unique microstructure: microparticles covered by finer nanoparticles on top. Electrochemical measurements demonstrate that the kinetics of the HER is significantly accelerated after bare copper is treated and turned black. At -0.325 V (v.s. RHE) in 1 M KOH aqueous solution, the calculated area-specific charge transfer resistance of the electrode decreases sharply from 159 Ω cm2 for the untreated copper to 1 Ω cm2 for the black copper. The electrochemical surface area of the black copper is measured to be only 2.4 times that of the untreated copper and therefore, the significantly enhanced electrocatalytic activity of the black copper for HER is mostly a result of its unique microstructure that favors the formation and enrichment of protons on the surface of copper. This work provides a new strategy for developing high-efficient electrodes for hydrogen generation.
RESUMEN
Optical coatings are integral components of virtually every optical instrument. However, despite being a century-old technology, there are only a handful of optical coating types. Here, we introduce a type of optical coatings that exhibit photonic Fano resonance, or a Fano-resonant optical coating (FROC). We expand the coupled mechanical oscillator description of Fano resonance to thin-film nanocavities. Using FROCs with thicknesses in the order of 300 nm, we experimentally obtained narrowband reflection akin to low-index-contrast dielectric Bragg mirrors and achieved control over the reflection iridescence. We observed that semi-transparent FROCs can transmit and reflect the same colour as a beam splitter filter, a property that cannot be realized through conventional optical coatings. Finally, FROCs can spectrally and spatially separate the thermal and photovoltaic bands of the solar spectrum, presenting a possible solution to the dispatchability problem in photovoltaics, that is, the inability to dispatch solar energy on demand. Our solar thermal device exhibited power generation of up to 50% and low photovoltaic cell temperatures (~30 °C), which could lead to a six-fold increase in the photovoltaic cell lifetime.
RESUMEN
Optical activation of material properties illustrates the potentials held by tuning light-matter interactions with impacts ranging from basic science to technological applications. Here, we demonstrate for the first time that composite nanostructures providing nonlocal environments can be engineered to optically trigger photoinduced charge-transfer-dynamic modulations in the solid state. The nanostructures explored herein lead to out-of-phase behavior between charge separation and recombination dynamics, along with linear charge-transfer-dynamic variations with the optical-field intensity. Using transient absorption spectroscopy, up to 270% increase in charge separation rate is obtained in organic semiconductor thin films. We provide evidence that composite nanostructures allow for surface photovoltages to be created, which kinetics vary with the composite architecture and last beyond optical pulse temporal characteristics. Furthermore, by generalizing Marcus theory framework, we explain why charge-transfer-dynamic modulations can only be unveiled when optic-field effects are enhanced by nonlocal image-dipole interactions. Our demonstration, that composite nanostructures can be designed to take advantage of optical fields for tuneable charge-transfer-dynamic remote actuators, opens the path for their use in practical applications ranging from photochemistry to optoelectronics.
RESUMEN
Femtosecond (fs) laser processing can significantly alter the optical, thermal, mechanical, and electrical properties of materials. Here, we show that fs-laser processing transforms aluminum (Al) to a highly efficient and multipronged heat exchanger. By optimizing the formed surface nano- and microstructures, we increase the Al emissivity and surface area by 700% and 300%, respectively. Accordingly, we show that fs-laser treated Al (fs-Al) increases the radiative and convective cooling power of fs-Al by 2100% and 300%, respectively, at 200 °C. As a direct application, we use fs-Al as a heat sink for a thermoelectric generator (TEG) and demonstrate a 280% increase in the TEG output power compared to a TEG with an untreated Al heat exchanger at 200 °C. The multipronged enhancement in fs-Al heat exchange properties lead to an increase in the TEG output power over a wide temperature ( T ) range ( T > 50 °C ). Conversely, a simple radiative cooling heat exchanger increases the TEG output power within a limited temperature range ( T > 150 °C ) . We investigate the laser processing parameters necessary to maximize the spectral emissivity and surface area of fs-Al. Fs-Al promises to be a widely used and compact heat exchanger for passive cooling of computers and data centers as well as to increase the efficiency of TEGs incorporated in sensors and handheld electronics.
RESUMEN
Femtosecond laser-induced surface structuring is a promising technique for the large-scale formation of nano- and microscale structures that can effectively modify materials' optical, electrical, mechanical, and tribological properties. Here we perform a systematic study on femtosecond laser-induced surface structuring on gold (Au) surface and their effect on both hydrophobicity and bacterial-adhesion properties. We created various structures including subwavelength femtosecond laser-induced periodic surface structures (fs-LIPSSs), fs-LIPSSs covered with nano/microstructures, conic and 1D-rod-like structures ( ≤ 6 µm), and spherical nanostructures with a diameter ≥ 10 nm, by raster scanning the laser beam, at different laser fluences. We show that femtosecond laser processing turns originally hydrophilic Au to a superhydrophobic surface. We determine the optimal conditions for the creation of the different surface structures and explain the mechanism behind the formed structures and show that the laser fluence is the main controlling parameter. We demonstrate the ability of all the formed surface structures to reduce the adhesion of Escherichia coli (E. coli) bacteria and show that fs-LIPSSs enjoys superior antibacterial adhesion properties due to its large-scale surface coverage. Approximately 99.03% of the fs-LIPSSs surface is free from bacterial adhesion. The demonstrated physical inhibition of bacterial colonies and biofilm formation without antibiotics is a crucial step towards reducing antimicrobial-resistant infections.
RESUMEN
Direct femtosecond (fs) laser processing is a maskless fabrication technique that can effectively modify the optical, electrical, mechanical, and tribological properties of materials for a wide range of potential applications. However, the eventual implementation of fs-laser-treated surfaces in actual devices remains challenging because it is difficult to precisely control the surface properties. Previous studies of the morphological control of fs-laser-processed surfaces mostly focused on enhancing the uniformity of periodic microstructures. Here, guided by the plasmon hybridisation model, we control the morphology of surface nanostructures to obtain more control over spectral light absorption. We experimentally demonstrate spectral control of a variety of metals [copper (Cu), aluminium (Al), steel and tungsten (W)], resulting in the creation of broadband light absorbers and selective solar absorbers (SSAs). For the first time, we demonstrate that fs-laser-produced surfaces can be used as high-temperature SSAs. We show that a tungsten selective solar absorber (W-SSA) exhibits excellent performance as a high-temperature solar receiver. When integrated into a solar thermoelectric generation (TEG) device, W-SSA provides a 130% increase in solar TEG efficiency compared to untreated W, which is commonly used as an intrinsic selective light absorber.
RESUMEN
The study of femtosecond laser structural coloring has recently attracted a great amount of research interest. These studies, however, have only been carried out in air. At the same time, laser ablation has also been actively studied in liquids as they provide a unique environment for material processing. However, surprisingly, structural coloring has never been performed in liquids. In this work, we perform the first study of metal structural coloring in liquid and compare the results to metal structural coloring in air. Colors created in liquid are formed by nanoparticle-induced plasmonic absorption and result in a range of colors transitioning from purple to orange. Surface structures formed in liquid are less hierarchical and more uniform than those formed in air, producing a surface with a much higher reflectance due to reduced light trapping, resulting in a more vibrant color. However, colorization formed in water suffers from less uniform colorization due to turbulence at the air-water and water-target interfaces, resulting in slight changes to the laser beam's focus during processing. Finally, finite-difference-time-domain simulation based on the measured surface structures is used to understand the role of plasmonic resonance in colorization.
RESUMEN
The fabrication of subwavelength two-dimensional (2D) structures on metals is of paramount importance to modern nanophotonics. Here we report a method to fabricate 2D conic structures on nickel surfaces using a single beam with three temporally delayed pulses. The 2D structures are fabricated over the entire irradiated region with relatively high uniformity. By controlling the delay between the three pulses, we control the effect of each pulse in creating laser-induced periodic surface structures which enables the control of the 2D structure features, namely, the period and structure dimensions. We explain the results based on the surface plasmon polariton-femtosecond laser interference model.