Search Results (32)

Hierarchical surface structuring is a critical aspect of advanced materials design, impacting fields ranging from optics to biomimetics. Among several laser-based methods for complex structuring of photo-responsive surfaces, the broadband vectorial interferometry proposed here offers unique performances. Such a method leverages a polychromatic laser source, an unconventional choice for holographic encoding, to achieve deterministic multiscale surface structuring through interference light patterning. Azopolymer films are used as photosensitive substrates. By exploring the interaction between optomechanical stress modulations at different spatial periodicities induced within the polymer bulk, we demonstrate the emergence of hierarchical Fourier surfaces composed of multiple deterministic levels. These structures range from sub-micrometer to tens of micrometers scale, exhibiting a high degree of control over their morphology. The experimental findings reveal that the optical encoding scheme significantly influences the resulting topographies. The polarization light patterns lead to more regular and symmetric hierarchical structures compared to those obtained with intensity patterns, underscoring the role of vectorial light properties in controlling surface morphologies. The proposed method is fully scalable, compatible with more complex recording schemes (including multi-beam interference), and it is applicable to a wide range of advanced technological fields. These include optics and photonics (diffractive elements, polarimetric devices), biomimetic surfaces, topographical design, information encoding, and anti-counterfeiting, offering a rapid, reliable, and versatile strategy for high-precision surface structuring at a submicrometric scale. Full article

In this work, we study the polarization properties of diffraction gratings recorded in thin films of the azopolymer PAZO (poly[1-[4-(3-carboxy-4-hydroxyphenylazo)benzene sulfonamido]-1,2-ethanediyl, sodium salt]) using digital polarization holography. Using two quarter-wave plates, the phase retardation of each pixel of the SLM is converted into the azimuth rotation of linearly polarized light. When recording from the azopolymer side of the sample, significant surface relief amplitude is observed with atomic force microscopy. In contrast, recording from the substrate side of the sample allows the reduction of the surface relief modulation and the obtaining of polarization gratings with characteristics close to an ideal grating, recorded with two orthogonal circular polarizations. This can be achieved even with a four-pixel period of grating, as demonstrated by our results. Full article

Significant research endeavors have been devoted to developing adhesives with reversible switching capabilities, allowing them to activate adhesion in response to diverse environmental stimuli. Among these, photo-switchable adhesives stand out as particularly promising. The presence of a photo-reversible solid-to-liquid transition, characterized by a transition temperature (T_SL), in certain azobenzene-containing polymers offers a compelling avenue for creating such adhesives. The development of a method based on Atomic Force Microscopy to measure both the glass transition temperature (T_g) and T_SL provided an opportunity to investigate the impact of various structural parameters on the solid-to-liquid transition of azopolymers. Our findings revealed that increasing the molecular weight (Mn) from 3400 to 8100 g/mol needed to achieve a highly cohesive adhesive resulted in an elevation in T_SL (>10 °C), making the solid-to-liquid transition at room temperature more challenging. However, incorporating a highly flexible substituent at the para position of the azobenzene group proved effective in significantly reducing the T_SL value (from 42 °C to 0 °C). This approach allows for the creation of photo-switchable adhesives with intriguing properties. We believe that our results establish a pathway toward developing a robust room-temperature photo-switchable adhesive. Full article

Orbital angular momentum (OAM) encoding is a promising technique to boost data transmission capacity in optical communications. Most recently, azobenzene films have gained attention as a versatile tool for creating and altering OAM-carrying beams. Unique features of azobenzene films make it possible to control molecular alignment through light-induced isomerization about the azo bond. This feature enables the fabrication of diffractive optical devices such as spiral phase plates and holograms by accurately imprinting a phase profile on the incident light. By forming azobenzene sheets into diffractive optical elements, such as spiral phase plates, one can selectively create OAM-carrying beams. Due to the helical wavefront and phase variation shown by these beams, multiple distinct channels can be encoded within a single optical beam. This can significantly increase the data transmission capacity of optical communication systems with this OAM multiplexing technique. Additionally, holographic optical components made from azobenzene films can be used to build and reconstruct intricate wavefronts. It is possible to create OAM-based holograms by imprinting holographic designs on azobenzene films, which makes it simpler to control and shape optical beams for specific communication requirements. In addition, azobenzene-based materials can then be suitable for integration into optical communication devices because of their reconfigurability, compactness, and infrastructure compatibility, which are the main future perspectives for achieving OAM-based technologies for the next generation, among other factors. In this paper, we see the possible use of azobenzene films in the generation and modification of OAM beams for optical communications through light-induced isomerization. In addition, the potential role of azobenzene films in the development of novel OAM-based devices that paves the way for the realization of high-capacity, OAM-enabled optical communication networks are discussed. Full article

Photoanisotropic materials, in particular azodyes and azopolymers, have attracted significant research interest in the last decades. This is due to their applications in polarization holography and 4G optics, enabling polarization-selective diffractive optical elements with unique properties, including circular polarization beam-splitters, polarization-selective bifocal lenses, and many others. Numerous methods have been applied to increase the photoinduced birefringence of these materials, and as a result, to obtain polarization holographic elements with a high diffraction efficiency. Recently, a new approach has emerged that has been extensively studied by many research groups, namely doping azobenzene-containing materials with nanoparticles with various compositions, sizes, and morphologies. The resulting nanocomposites have shown significant enhancement in their photoanisotropic response, including increased photoinduced birefringence, leading to a higher diffraction efficiency and a larger surface relief modulation in the case of polarization holographic recordings. This review aims to cover the most important achievements in this new but fast-growing field of research and to present an extensive comparative analysis of the result, reported by many research groups during the last two decades. Different hypotheses to explain the mechanism of photoanisotropy enhancement in these nanocomposites are also discussed. Finally, we present our vision for the future development of this scientific field and outline its potential applications in advanced photonics technologies. Full article

During polarization holographic recording in azopolymer thin films, usually together with the volume anisotropic grating, a surface relief grating (SRG) is also formed. By using two consecutive exposures, it is possible to obtain a two-dimensional (2D) grating. To the best of our knowledge, the polarization properties of such gratings have not been studied yet. To determine the influence of the surface relief on the polarization selectivity of the 2D gratings, we propose two methods to suppress the SRG formation: by varying the recording conditions or varying the sample structure. In these experiments we have used the commercially available azopolymer PAZO, poly[1-4-(3-carboxy-4-hydrophenylazo) benzene sulfonamido]-1,2-ethanediyl, sodium salt] to perform the polarization holographic recording using a 442 nm He-Cd laser. As indicated by our results, when the surface relief is present, it strongly dominates the response of the 2D grating and it behaves almost as a scalar polarization insensitive grating. Conversely, when the SRG formation is suppressed, the polarization properties of the 2D grating in all four diffracted orders are very well pronounced. In this way, we demonstrate that we can easily control SRG formation and, if desired, obtain 2D grating with high surface relief modulation, or alternatively record polarization-selective 2D gratings with virtually no surface relief. Full article

We study Monte Carlo dynamics of the monomers and center of mass of a model polymer chain functionalized with azobenzene molecules in the presence of an inhomogeneous linearly polarized laser light. The simulations use a generalized Bond Fluctuation Model. The mean squared displacements of the monomers and the center of mass are analyzed in a period of Monte Carlo time typical for a build-up of Surface Relief Grating. Approximate scaling laws for mean squared displacements are found and interpreted in terms of sub- and superdiffusive dynamics for the monomers and center of mass. A counterintuitive effect is observed, where the monomers perform subdiffusive motion but the resulting motion of the center of mass is superdiffusive. This result disparages theoretical approaches based on an assumption that the dynamics of single monomers in a chain can be characterized in terms of independent identically distributed random variables. Full article

The measurement of the refractive index typically requires the use of optical ellipsometry which, although potentially very accurate, is extremely sensitive to the structural properties of the sample and its theoretical modeling, and typically requires specialized expertise to obtain reliable output data. Here, we propose a simple diffractive method for the measurement of the refractive index of homogenous solid thin films, which requires only the structuring of the surface of the material to be measured with the profile of a diffraction grating. The refractive index of an exemplary soft-moldable material is successfully estimated over a wide wavelength range by simply incorporating the measured topography and diffraction efficiency of the grating into a convenient scalar theory-based diffraction model. Without the need for specialized expertise and equipment, the method can serve as a simple and widely accessible optical characterization of materials useful in material science and photonics applications. Full article

Recently, the realization of the spiral mass transfer of matter has attracted the attention of many researchers. Nano- and microstructures fabricated with such mass transfer can be used for the generation of light with non-zero orbital angular momentum (OAM) or the sensing of chiral molecules. In the case of metals and semiconductors, the chirality of formed spiral-shaped microstructures depends on the topological charge (TC) of the illuminating optical vortex (OV) beam. The situation is quite different with polarization-sensitive materials such as azopolymers, azobenzene-containing polymers. Azopolymers show polarization-sensitive mass transfer both at the meso and macro levels and have huge potential in diffractive optics and photonics. Previously, only one-spiral patterns formed in thin azopolymer films using circularly polarized OV beams and double-spiral patterns formed using linearly polarized OV beams have been demonstrated. In these cases, the TC of the used OV beams did not affect the number of formed spirals. In this study, we propose to use two-beam (an OV and a Gaussian beam with a spherical wavefront) interference lithography for realization spiral mass transfer with the desired number of formed spirals. The TC of the OV beam allows for controlling the number of formed spirals. We show the microstructures fabricated by the laser processing of thin azopolymer films can be used for the generation of OAM light at the microscale with the desired TC. The experimentally obtained results are in good agreement with the numerically obtained results and demonstrate the potential of the use of such techniques for the laser material processing of polarization-sensitive materials. Full article

We report on solving of two intriguing issues concerning the inscription of surface relief gratings within azopolymer thin films under irradiation with SS, PP and RL interference patterns. For this, we utilize the orientation approach and viscoplastic modeling in combination with experimental results, where the change in surface topography is acquired in situ during irradiation with modulated light. First, the initial orientation state of polymer backbones is proved to be responsible for the contradictory experimental reports on the efficiency of the SS interference pattern. Different orientation states can influence not only the phase of SS grating but also its height, which is experimentally confirmed by using special pretreatments. Second, the faster growth of gratings inscribed by the RL interference pattern is shown to be promoted by a weak photosoftening effect. Overall, the modeled results are in good agreement with the order of relative growth efficiency: RL–PP–SS. Full article

Azobenzene-containing polymers (azo-polymers) have been a subject of extensive investigations during the last two and half decades, due to their remarkable ability to undergo pronounced alignment and deformation under irradiation with light. The molecular ordering and deformation in azo-polymers of various structures under irradiation with linearly polarized light was described in a series of theoretical works, based on the effect of the reorientation of azobenzene moieties due to the anisotropic character of the photoisomerization processes. In the present study, we generalize the previous orientation approach to describe the photo-alignment and deformation of azo-polymer networks under irradiation with elliptically polarized light. We demonstrate that, in general, the light-induced ordering and deformation have a biaxial symmetry defined by the polarization ellipse. Azobenzene chromophores have a tendency to align along the direction of light propagation, the orientation in the other two directions being dependent of the aspect ratio of the polarization ellipse. This causes deformation of azo-polymer networks along the direction of light propagation, the sign of which (expansion/contraction) is defined by a chemical structure of network strands. Theoretical results are in agreement with experiments and have a practical importance to predict the photo-mechanical response of azo-polymers depending on their structure and on the polarization of light. Full article

Photoactive polymers are important for fundamental studies and applications in several area of photonics such as data storage and holography and nonlinear optics and photomechanics. The latter is perhaps one of the most important applications of such materials, since they act as light to mechanical energy transducers and move under light action. For example, azo-polymers irradiated by inhomogeneous resonant ultra-violet or visible light undergo molecular and macroscopic motion, at sub-glass transition temperatures by photoisomerization of the azo dyes. Our recent research in this field highlighted the fundamentals of mobility enhancement by light, including light-induced viscosity change and acceleration of relaxation times, and photomechanics, encompassing motions in gradients of actinic light leading to surface structuring and actuation. In this paper, we present an original model which predicts the creation of mechanical pressure, i.e., motion, by a photo-induced change in the occupied volume and length of anisometric isomers, and we give simple analytical expressions describing the dynamics of volume as well as strain change upon polarized light irradiation of photomechanic samples. Full article

The polarization sensitivity of azopolymers is well known. Therefore, these materials are actively used in many applications of photonics. Recently, the unique possibilities of processing such materials using a structured laser beam were demonstrated, which revealed the key role of the distribution of polarization and the longitudinal component of light in determining the shape of the nano- and microstructures formed on the surfaces of thin azopolymer films. Here, we present numerical and experimental results demonstrating the high polarization sensitivity of thin azopolymer films to the local polarization state of an illuminating structured laser beam consisting of a set of light spots. To form such arrays of spots with a controlled distribution of polarization, different polarization states of laser beams, both homogeneous and locally inhomogeneous, were used. The results obtained show the possibility of implementing a parallel non-uniform patterning of thin azopolymer films depending on the polarization distribution of the illuminating laser beam. We believe that the demonstrated results will not only make it possible to implement the simultaneous detection of local polarization states of complex-shaped light fields but will also be used for the high-performance fabrication of diffractive optical elements and metasurfaces. Full article

Notwithstanding the significant optical applicability of PAZO polymer films, there are no accurate data about their optical characteristics. To remedy this shortcoming, in this study three PAZO polymer thin films are characterized, with dissimilar thicknesses, on glass substrates using only one UV/VIS/NIR transmittance spectrum T(λ) per sample and an original hybrid dispersion model (HDM). HDM is based on the Tauc–Lorentz model, the new amorphous dispersion formula, the Tauc–Lorentz–Urbach model of Foldyna and the Tauc–Lorentz–Urbach model of Rodriguez. HDM with two oscillators is employed in characterizations of the PAZO polymer films in the range [300, 2500] nm, whereby the root-mean-square deviation (RMSD) of the fitted transmittance spectrum with respect to T(λ) does not exceed 1.6 × 10⁻³. Decreasing RMSD by 2.3% to 94.4% is demonstrated by employing HDM compared with the above mentioned four popular dispersion models, for each one of the studied films. HDM is applicable to amorphous films independent of their thickness as well as to cases of non-transparent substrate. Full article

Azo molecules, characterized by the presence of a -N=N- double bond, are widely used in various fields due to their sensitivity to external stimuli, ch as light. The emergence of bacterial resistance has pushed research towards designing new antimicrobial molecules that are more efficient than those currently in use. Many authors have attempted to exploit the antimicrobial activity of azobenzene and to utilize their photoisomerization for selective control of the bioactivities of antimicrobial molecules, which is necessary for antibacterial therapy. This review will provide a systematic and consequential approach to coupling azobenzene moiety with active antimicrobial molecules and drugs, including small and large organic molecules, such as peptides. A selection of significant cutting-edge articles collected in recent years has been discussed, based on the structural pattern and antimicrobial performance, focusing especially on the photoactivity of azobenzene and the design of smart materials as the most targeted and desirable application. Full article