Publications by authors named "Milichko V"

Metal-organic frameworks (MOFs) form a unique platform for operation with data using ReRAM technology. Here we report on a large-scale fabrication of a MOF-based ReRAM array with 6 × 6 cells, demonstrating 50% variation in their electronic parameters. Despite this inhomogeneity, such a "non-ideal" ReRAM array is used for recording binary information followed by deep learning processes to achieve 95% accuracy of reading.

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The design of fast, endurant, and biocompatible porous frameworks with solvatochromism, aimed to addressing the multiple visual sensing of chemicals, still remains a challenge. Here, we report on a solvatochromic metal-organic framework (MOF) based on cobalt and trimesic acid. We examined its solvatochromism through the solvent exchange and revealed high selectivity to water/dimethylformamide combination.

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Optical clearing of invertebrates, the number of species of which is 20 times greater than that of vertebrates, is of fundamental and applied interest for neuroscience in general. Herein, the optical clearing of invertebrates to identify their morphology and neurostructure remains unrealized as of yet. Here, we report on fast (from a few seconds to minutes) and uniform whole-body optical clearing of invertebrates (bivalves, nemertines, annelids, and anomura) of any age and thickness (up to 2 cm) possessing complicated structures and integuments.

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The synthesis of bioinspired metal-organic frameworks (MOFs) performed in mild conditions with a high quality is greatly demanded. Moreover, the influence of the morphology and structure of bio-MOFs on the cell interaction and toxicity is important to determine. In this work, we developed an ultrasound (US)-assisted synthesis of HKUST-1 MOFs under mild conditions and investigated the influence of the parameters of synthesis on the morphology, structure, and biological properties of the developed MOFs.

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Metal-organic frameworks (MOFs) possess a virtually unlimited number of potential structures. Although the latter enables an efficient route to control the structure-related functional properties of MOFs, it still complicates the prediction and searching for an optimal structure for specific application. Next to prediction of the MOFs for gas sorption/separation and catalysis via machine learning (ML), we report on ML to find MOFs demonstrating a phase transition (PT).

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Article Synopsis
  • The DUT-4 metal-organic framework (MOF) undergoes a structural transformation from an ordered to a distorted phase when exposed to ambient conditions.
  • Various analytical techniques, including X-ray diffraction, Raman and FTIR spectroscopy, scanning electron microscopy, and thermal analysis, were utilized to study this transformation.
  • The phase transition responds reversibly to factors like exposure time and humidity, indicating potential for new MOF-based materials in optoelectronic applications.
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Control of the optical properties of a nanoparticle (NP) through its structural changes underlies optical data processing, dynamic coloring, and smart sensing at the nanometer scale. Here, we report on the concept of controlling the light scattering by a NP through mixing of weakly miscible chemical elements (Fe and Au), supporting a thermal-induced phase transformation. The transformation corresponds to the transition from a homogeneous metastable solid solution phase of the (Fe,Au) NP towards an equilibrium biphasic Janus-type NP.

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Laser conversion of metal-organic frameworks (MOFs) has recently emerged as a fast and low-energy consumptive approach to create scalable MOF derivatives for catalysis, energy, and optics. However, due to the virtually unlimited MOF structures and tunable laser parameters, the results of their interaction are unpredictable and poorly controlled. Here, we experimentally base a general approach to create nano- to centimeter-scale MOF derivatives with the desired nonlinear optical and catalytic properties.

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Two-dimensional metal-organic frameworks (MOFs) occupy a special place among the large family of functional 2D materials. Even at a monolayer level, 2D MOFs exhibit unique sensing, separation, catalytic, electronic, and conductive properties due to the combination of porosity and organo-inorganic nature. However, lab-to-fab transfer for 2D MOF layers faces the challenge of their scalability, limited by weak interactions between the organic and inorganic building blocks.

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We report on the design of 1D MOFs based on a nopinane-annelated organic ligand and Co(II) or Ni(II), the variation of which allows tuning the optical modulation bandwidth. Structural and time-resolved analysis revealed the optical modulation mechanism, the rates and its endurance, thereby enriching the list of sustainable MOFs for tunable optical modulators.

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Nanocrystalline titanium dioxide (TiO) is a widespread multifunctional and environmentally friendly material that has numerous applications requiring micro-/nanofabrication or thin film deposition. In most cases, the fabrication of titania films can be achieved using cost-efficient solution chemistry combined with various coating or printing techniques. The practical implementation of these methods requires the preparation of a suitable ink with properly adjusted rheological properties.

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A family of coordination polymers (CPs) based on dynamic structural elements are of great fundamental and commercial interest addressing modern problems in controlled molecular separation, catalysis, and even data processing. Herein, the endurance and fast structural dynamics of such materials at ambient conditions are still a fundamental challenge. Here, we report on the design of a series of Cu-based CPs [Cu(bImB)Cl] and [Cu(bImB)Cl] with flexible ligand bImB (1,4-bis(imidazol-1-yl)butane) packed into one- and two-dimensional (1D, 2D) structures demonstrating dimensionality mediated flexibility and reversible structural transformations.

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Metal-organic frameworks (MOFs) have been recently explored as crystalline solids for conversion into amorphous phases demonstrating non-specific mechanical, catalytic, and optical properties. The real-time control of such structural transformations and their outcomes still remain a challenge. Here, we use high-resolution transmission electron microscopy with 0.

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Photoinduced modulation of the optical parameters of nanomaterials underlies the operating principles of all-optical nanodevices. Here, we demonstrate the laser-induced 10% modulation of the refractive index and 16-fold modulation of the extinction coefficient of the dynamic metal-organic framework (HKUST-1) nanocrystals within the whole visible range. Using the laser-induced water sorption/desorption process inside HKUST-1, we have achieved size-dependent reversible tuning of brightness and color of its nanocrystals over the different spatial directions and color palette.

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Time-resolved optical emission spectroscopy of nanosecond-pulsed discharges ignited in liquid nitrogen between two bismuth electrodes is used to determine the main discharge parameters (electron temperature, electron density and optical thickness). Nineteen lines belonging to the Bi I system and seven to the Bi II system could be recorded by directly plunging the optical fibre into the liquid in close vicinity to the discharge. The lack of data for the Stark parameters to evaluate the broadening of the Bi I lines was solved by taking advantage of the time-resolved information supported by each line to determine them.

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Active controlling of optical properties of metallic particles holds great promise for nonlinear nanophotonics and compact optoelectronic devices. Except for the electronic and chemical tuning of their properties, active control through fast and reversible shape modulation remains a significant challenge. Here, we report on the concept for changing the color and brightness of single particles by reversible/irreversible tuning of their shapes.

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We suggest a new strategy for creating stimuli-responsive bio-integrated optical nanostructures based on Mie-resonant silicon nanoparticles covered by an ensemble of similarity negatively charged polyelectrolytes (heparin and sodium polystyrene sulfonate). The dynamic tuning of the nanostructures' optical response is due to light-induced heating of the nanoparticles and swelling of the polyelectrolyte shell. The resulting hydrophilic/hydrophobic transitions significantly change the shell thickness and reversible shift of the scattering spectra for individual nanoparticles up to 60 nm.

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Glial cells are the most abundant cells in both the peripheral and central nervous systems. During the past decade, a subpopulation of immature peripheral glial cells, namely, embryonic Schwann cell-precursors, have been found to perform important functions related to development. These cells have properties resembling those of the neural crest and, depending on their location in the body, can transform into several different cell types in peripheral tissues, including autonomic neurons.

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This study addresses the inkjet printing approach for fabrication of cellulose nanocrystalline (CNC) patterns with tunable optical properties varied by the thickness of deposited layers. In particular, forming functional patterns visible only in linearly polarized light is of the primary interest. The possibility of controlling the bright iridescent color response associated with the birefringence in the chiral anisotropic structure of inkjet-printed layers of CNC with sulfo-groups (s-CNC) has been thoroughly investigated.

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Polymers with embedded metal-organic frameworks (MOFs) have been of interest in research for advanced applications in gas separation, catalysis and sensing due to their high porosity and chemical selectivity. In this study, we utilize specific MOFs with high thermal stability and non-centrosymmetric crystal structures (zeolitic imidazolate framework, ZIF-8) in order to give an example of MOF-polymer composite applications in nonlinear optics. The synthesized MOF-based polymethyl methacrylate (PMMA) composite (ZIF-8-PMMA) demonstrates the possibility of the visualization of near-infrared laser beams in the research lab.

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We demonstrate herein an all-optical switch based on stimuli-responsive and photochromic-free metal-organic framework (HKUST-1). Ultrafast near-infrared laser pulses stimulate a reversible 0.4 eV blue shift of the absorption band with up to 200 s rate due to dehydration and concomitant shrinking of the structure-forming [Cu C O ] cages of HKUST-1.

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In the drill core of the Kola super-deep borehole (SG-3, 12,262 m depth) gold-bearing rocks of Archaean age have been located at depths of 9,500 to 11,000 m. In veins, between 9,052 and 10,744 m, within this gold zone, quartz contains fluid inclusions with gold nanoparticles. There are 4 types of fluid inclusions (1) gas inclusions of dense CO, (2) liquid-vapor two-phase aqueous inclusions, (3) three-phase inclusions with NaCl daughter crystals, and (4) CO-aqueous inclusions.

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Owing to the synergistic combination of a hybrid organic-inorganic nature and a chemically active porous structure, metal-organic frameworks have emerged as a new class of crystalline materials. The current trend in the chemical industry is to utilize such crystals as flexible hosting elements for applications as diverse as gas and energy storage, filtration, catalysis, and sensing. From the physical point of view, metal-organic frameworks are considered molecular crystals with hierarchical structures providing the structure-related physical properties crucial for future applications of energy transfer, data processing and storage, high-energy physics, and light manipulation.

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Correction for 'Laser printing of optically resonant hollow crystalline carbon nanostructures from 1D and 2D metal-organic frameworks' by Leila R. Mingabudinova et al., Nanoscale, 2019, 11, 10155-10159.

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Using a hybrid approach involving a slow diffusion method to synthesize 1D and 2D MOFs followed by their treatment with femtosecond infrared laser radiation, we generated 100-600 nm well-defined hollow spheres and hemispheres of graphite. This ultra-fast technique extends the library of shapes of crystalline MOF derivatives appropriate for all-dielectric nanophotonics.

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