Alexey Zhizhchenko

Laser patterning technologies for halide perovskite materials have recently shown significant progress due to their optimal combination of cost, performance and resolution. Nevertheless, due to the relative novelty of the material, some aspects of laser structuring of perovskites have not yet been studied. Some of the most important parameters of the fabrication method is the roughness of the treated surface and the number of structural defects that negatively affect the characteristics of manufactured devices. This paper presents for the first time the results of laser structuring of CsPbBr₃ perovskite microcrystals using ultraviolet femtosecond radiation with a wavelength of 257 nm. The possibility of creating structures on the surface of single microcrystals with submicrometer resolution without visible deterioration of the photoluminescent properties of the material, despite the high photosensitivity of the material to this wavelength range, is shown. The created structures have an extremely low roughness comparable to the roughness of the initial surface of monocrystals, which is unusual for direct laser ablation processing methods and has great potential for fabrication of perovskite nanophotonics elements.

At the moment, manipulation of liquid microdroplets is required in various microfluidic and lab-on-a-chip devices, as well as advanced sensors. We report a new method for microdroplets manipulation, based on the use non-uniform electrostatic fields. Our platform uses an electrode array embedded in a dielectric planar superhydrophobic substrate produced by direct laser writing. When a voltage is applied to a certain sequence of electrodes, a non-uniform electrostatic field is produced, which acts to attract a droplet on the substrate to the electrodes. This achieves a stepwise movement of the droplet. We realized non-contact, selective and high-speed movement of the individual droplets along specified trajectories and their selective coalescence. In our opinion, this approach has a huge potential for chemical technology applications especially in optical sensors.

We present the results of direct laser-induced periodic surface structuring of semiconductors thin films (a-Si, a-Ge) deposited on glass substrate at different ambient environments (air, vacuum, nitrogen) resulting in regular gratings with the period of 600 nm to 900 nm at the laser wavelength of 1026 nm oriented either along (a-Si) or transverse (a-Ge) to the linear laser polarization direction. The processing speed has a different effect on morphology of obtained structures: on a-Si film, an increase of scanning speed leads to the reorientation of gratings and reduction of their period, while on a-Ge, the uniformity degradation and increase of the period are observed. Changing the ambient atmosphere from air to nitrogen and vacuum, when writing structures on a-Ge, helps to minimize the uniformity degradation and obtain highly regular nanogratings.

One of the promising novel methods for radical tumor resection at a single-cell level is magneto-mechanical microsurgery (MMM) with magnetic nano- or microdisks modified with cancer-recognizing molecules. A low-frequency alternating magnetic field (AMF) remotely drives and controls the procedure. Here, we present characterization and application of magnetic nanodisks (MNDs) as a surgical instrument (“smart nanoscalpel”) at a single-cell level. MNDs with a quasi-dipole three-layer structure (Au/Ni/Au) and DNA aptamer AS42 (AS42-MNDs) on the surface converted magnetic moment into mechanical and destroyed tumor cells. The effectiveness of MMM was analyzed on Ehrlich ascites carcinoma (EAC) cells in vitro and in vivo using sine and square-shaped AMF with frequencies from 1 to 50 Hz with 0.1 to 1 duty-cycle parameters. MMM with the “Nanoscalpel” in a sine-shaped 20 Hz AMF, a rectangular-shaped 10 Hz AMF, and a 0.5 duty cycle was the most effective. A sine-shaped field caused apoptosis, whereas a rectangular-shaped field caused necrosis. Four sessions of MMM with AS42-MNDs significantly reduced the number of cells in the tumor. In contrast, ascites tumors continued to grow in groups of mice and mice treated with MNDs with nonspecific oligonucleotide NO-MND. Thus, applying a “smart nanoscalpel” is practical for the microsurgery of malignant neoplasms.

At the moment, manipulation of liquid microdroplets is required in various microfluidic and lab-on-a-chip devices, as well as advanced sensors. The platforms used for these purposes should provide the possibility of controlled selective movement and coalescence of droplets, and the manipulation speed should be sufficiently high (more than 10 mm/s). In addition, to facilitate their practical application, such platforms should have a simple planar geometry and low manufacturing cost. We report here a new method for microdroplet manipulation based on the use of non-uniform electrostatic fields. Our platform uses an electrode array embedded in a dielectric planar superhydrophobic substrate (50 × 50 mm). When a voltage is applied to a certain sequence of electrodes, a non-uniform electrostatic field is produced, which acts to attract a droplet on the substrate to the electrodes. This achieves a stepwise movement of the droplet. We realized non-contact, selective and high speed (up to 80 mm/s) movement of the individual droplets along specified trajectories (like a chess game) and their selective coalescence. It allowed us to demonstrate several controllable chemical reactions including an analytical one. In our opinion, this approach has a huge potential for chemical technology applications, especially in advanced sensors.

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.

Cell and tissue nanomechanics has been intriguingly introduced into biomedical research, not only complementing traditional immunophenotyping and molecular analysis, but also bringing unexpected new insights for clinical diagnostics and bioengineering. However, despite the progress in the study of individual cells in culture by atomic force microscopy (AFM), its application for mapping live tissues has a number of technical limitations. Here, we elaborate a new technique to study live slices of normal brain tissue and tumors by combining morphological and nanomechanical AFM mapping in high throughput scanning mode, in contrast to the typically utilized force spectroscopy mode based on single-point probe application. This became possible due to the combined use of an appropriate embedding matrix for vibratomy and originally modified AFM probes. The embedding matrix composition was carefully developed by regulating the amounts of agar and collagen I to reach optimal viscoelastic properties for obtaining high-quality live slices that meet AFM requirements. AFM tips were rounded by irradiating them with focused nanosecond laser pulses, while the resulting tip morphology was verified by scanning electron microscopy. Live slices preparation and AFM investigation take only 55 min and could be combined with a vital cell tracer analysis or immunostaining, thus making it promising for biomedical research and clinical diagnostics.

Recently, sensors using surface-enhanced Raman scattering (SERS) detectors combined with superhydrophobic/superhydrophilic analyte concentration systems showed the ability to reach detection limits below the femto-molar level. However, a further increase in the sensitivity of these sensors is limited by the impossibility of the concentration systems to deposit the analyte on an area of less than 0.01 mm². This article proposes a fundamentally new approach to the analyte enrichment, based on the effect of non-uniform electrostatic field on the evaporating droplet. This approach, combined with the optimized geometry of a superhydrophobic/superhydrophilic concentration system allows more than a six-fold reduction of the deposition area. Potentially, this makes it possible to improve the detection limit of the plasmonic sensors by the same factor, bringing it down to the attomolar level.

The optical response of properly excited periodically arranged plasmonic nanostructures is known to demonstrate sharp resonance features associated with high-Q collective modes demanding for various applications in light–matter interaction, filtering and sensing. Meanwhile, practical realization and replication of plasmonic platforms supporting high-Q modes via scalable inexpensive lithography-free approach is still challenging. Here, we justify direct ablation-free irradiation of Si-supported thin Au film by nanojoule-energy femtosecond laser pulses as a single-step and scalable technology for realization of plasmonic metasurfaces supporting collective plasmonic response. Using an adjustable aperture to control and upscale the size of the fabricated nanostructures, nanobumps and nanojets, we demonstrated plasmonic metasurface supporting collective resonances with a moderately high Q-factor (up to 17) and amplitude (up to 45%) within expanded spectral range (1.4–4.5 µm). Vacuum deposition of thin films above the as-fabricated nanostructure arrays was demonstrated to provide fine tuning of the resonance position, also expanding the choice of available materials for realization of plasmonic designs with extended functionality.

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.