Long-term stability in contact with water of organosilane layers formed by octadecyltrimethoxysilane (ODTMS) on polished aluminum alloy (AA2024) through dip-coating was studied by combining SEM, water contact angle measurements, and X-ray photoelectron spectroscopy. Similar organosilane layers were formed on AA2024 coated with permanganate conversion coating, 1,2-bis(triethoxysilyl)ethane (BTSE) and hydrated SiO_x as under-layers, after which their long-term durability was also tested. During immersion in water for about one month, all the samples exhibited a decrease in hydrophobicity, implying the prepared organosilane layer was not stable over time, gradually hydrolyzing and letting water interact with the underlying layer. In parallel, SEM images of one-layer samples taken after immersion showed clear signs of local electrochemical corrosion, while XPS analysis confirmed a loss of silicon from the surface layer. The highest stability over time was demonstrated by a one-layer sample prepared in an ethanol/water bath for 5 min and by a similar ODTMS layer prepared on hydrated MnO_x as an under-layer.

We report an easy-to-implement device for surface-enhanced Raman scattering (SERS)-based detection of various analytes dissolved in water droplets at trace concentrations. The device combines an analyte-enrichment system and SERS-active sensor site, both produced via inexpensive and high-performance direct femtosecond (fs)-laser printing. Fabricated on a surface of water-repellent polytetrafluoroethylene substrate as an arrangement of micropillars, the analyte-enrichment system supports evaporating water droplet in the Cassie–Baxter superhydrophobic state, thus ensuring delivery of the dissolved analyte molecules towards the hydrophilic SERS-active site. The efficient pre-concentration of the analyte onto the sensor site based on densely arranged spiky plasmonic nanotextures results in its subsequent label-free identification by means of SERS spectroscopy. Using the proposed device, we demonstrate reliable SERS-based fingerprinting of various analytes, including common organic dyes and medical drugs at ppb concentrations. The proposed device is believed to find applications in various areas, including label-free environmental monitoring, medical diagnostics, and forensics.

Controllable targeted deposition of an analyte dissolved in a liquid drop evaporating on a superhydrophobic surface has recently emerged as a promising concentrator approach with various applications ranging from ultrasensitive bioidentification to DNA molecule sorting. Here, we demonstrate that surface textures with non-uniform wettability fabricated using direct easy-to-implement femtosecond-pulse filament-assisted ablation of polytetrafluoroethylene substrates can be used to concentrate and deposit an analyte at a designated location out of a water droplet. The proposed surface textures contain a central superhydrophilic trap surrounded by superhydrophobic periodically arranged pillars with a hierarchical roughness. By optimizing the arrangement and geometry of the central trap and the surrounding superhydrophobic textures, the analyte dissolved in a 5 μL water drop was fixed onto a 90 × 90 μm² target. The proposed textures provide a concentration factor of 10³, an order of magnitude higher than those for the previously reported surface textures. This promising ultrasensitive versatile platform allows the detection of fingerprints of the deposited analyte via surface-enhanced spectroscopy techniques (Raman scattering or photoluminescence) at an estimated detection threshold better than 10⁻¹⁵ mol L⁻¹.

Ultrashort laser pulses deliver electromagnetic energy to matter causing its localized heating that can be used for both material removal via ablation/evaporation and driving interface chemical reactions. Here, it is shown that both mentioned processes can be simultaneously combined within straightforward laser nanotexturing of Si wafer in a functionalizing solution to produce a practically relevant metal–semiconductor surface nano‐morphology. Such unique hybrid morphology represents deep‐subwavelength Si laser‐induced periodic surface structures (LIPSSs) with an extremely short period down to 70 nm and high‐aspect‐ratio nano‐trenches loaded with controllable amount of plasmonic nanoparticles formed via laser‐induced decomposition of the precursor noble‐metal salts. Moreover, heat localization driving reduction process is utilized to produce surface morphology locally decorated with dissimilar plasmon‐active nanoparticles. Light‐absorbing deep‐subwavelength Si LIPSSs loaded with controllable amount of noble‐metal nanoparticles represent an attractive architecture for plasmon‐related applications such as optical nanosensing where efficient coupling of the propagating optical waves to highly localized electromagnetic “hot spots” is a mandatory requirement. To support this statement, applicability of such hybrid morphology for fluorescence‐based detection of nanomolar concentrations of mercury cations in solution is demonstrated.

Amorphous silicon ($\alpha$-Si) film present an inexpensive and promising material for optoelectronic and nanophotonic applications. Its basic optical and optoelectronic properties are known to be improved via phase transition from amorphous to polycrystalline phase. Infrared femtosecond laser radiation can be considered to be a promising nondestructive and facile way to drive uniform in-depth and lateral crystallization of $\alpha$-Si films that are typically opaque in UV-visible spectral range. However, so far only a few studies reported on use of near-IR radiation for laser-induced crystallization of $\alpha$-Si providing less information regarding optical properties of the resultant polycrystalline Si films demonstrating rather high surface roughness. The present work demonstrates efficient and gentle single-pass crystallization of $\alpha$-Si films induced by their direct irradiation with near-IR femtosecond laser pulses coming at sub-MHz repetition rate. Comprehensive analysis of morphology and composition of laser-annealed films by atomic-force microscopy, optical, micro-Raman and energy-dispersive X-ray spectroscopy, as well as numerical modeling of optical spectra, confirmed efficient crystallization of $\alpha$-Si and high-quality of the obtained films. Moreover, we highlight localized laser-induced crystallization of $\alpha$-Si as a promising way for optical information encryption, anti-counterfeiting and fabrication of micro-optical elements.

We demonstrate a multi-purpose plasmonic sensor based on a nanovoid array fabricated via inexpensive and highly-reproducible direct femtosecond laser patterning of thin glass-supported Au films. The proposed nanovoid array exhibits near-IR surface plasmon (SP) resonances, which can be excited under normal incidence and optimised for specific applications by tailoring the array periodicity, as well as the nanovoid geometric shape. The fabricated SP sensor offers competitive sensitivity of ≈ 1600 nm/RIU at a figure of merit of 12 in bulk refractive index tests, as well as allows for identification of gases and ultra-thin analyte layers, making the sensor particularly useful for common bioassay experiments. Moreover, isolated nanovoids support strong electromagnetic field enhancement at lattice SP resonance wavelength, allowing for label-free molecular identification via surface-enhanced vibration spectroscopy.