Search Results (75)

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

Hydrogen-bonded cross-linked main chain azobenzene (azo) photoactive polymers have broad application prospects in flexible actuators, optical actuators, and other fields. Most of the research on this kind of photoresponsive material is mainly focused on air, and exploration in solvents remains underexplored. In this paper, azobenzene polyamide ester semicrystalline polymer (PEA-6T) with hydrogen-bond cross-linking was synthesized by Michael addition polymerization. The uniaxially oriented polymer film with high orientation (48.85%) and fast response (5 s under UV light and 55 s under visible light) was obtained by a simple solution casting/mechanical stretching method. Compared with PEA-2T and PEA-4T, PEA-6T exhibits enhanced mechanical properties (elastic modulus increased by 17.4%; yield strength increased by 34.1%; breaking strength increased by 75.4%; elongation at break increased by 33.8%; toughness increased by 101.3%; photoinduced stress increased by 43.5%) and reduced light response time (decreased by 58.3% in ultraviolet light and 50% in visible light) due to the elongation of the compliant chain length. The thin PEA-6T film exhibited light-induced deformation not only in air but also in polar solvents such as water, methanol, ethanol, butanol, and saline solutions (e.g., normal saline, 0.9 wt% NaCl, and simulated seawater, 3.5 wt% NaCl). In addition, polarizing optical microscope (POM) observations showed that the brightness and texture direction of the films remained stable (Δ_Brightness < 5%), the light response time was consistent (6 s under UV light, 65 s under visible light), the light-induced stress retention rate was 95%, and the films exhibited good solvent resistance. This study bridges the research gap in azobenzene photoresponsive materials in solvent environments, and the material shows potential for applications in marine equipment coatings or biomedical actuators. Full article

Recent advancements in hybrid photonic integrated circuits (PICs) for wireless communications are reviewed, with a focus on innovations developed at Fraunhofer HHI. This work leverages hybrid integration technology, which combines indium phosphide (InP) active elements, silicon nitride (Si₃N₄) low-loss waveguides, and high-efficient thermal-optical tunable polymers with micro-optical functions to achieve fully integrated wireless transceivers. Key contributions include (1) On-chip optical injection locking for generating phase-locked optical beat notes at 45 GHz, enabled by cascaded InP phase modulators and hybrid InP/polymer tunable lasers with a 3.8 GHz locking range. (2) Waveguide-integrated THz emitters and receivers, featuring photoconductive antennas (PCAs) with a 22× improved photoresponse compared to top-illuminated designs, alongside scalable 1 × 4 PIN-PD and PCA arrays for enhanced power and directivity. (3) Beam steering at 300 GHz using a polymer-based optical phased array (OPA) integrated with an InP antenna array, achieving continuous steering across 20° and a 10.6 dB increase in output power. (4) Demonstration of fully integrated hybrid wireless transceiver PICs combining InP, Si₃N₄, and polymer material platforms, validated through key component characterization, on-chip optical frequency comb generation, and coherent beat note generation at 45 GHz. These advancements result in compact form factors, reduced power consumption, and enhanced scalability, positioning PICs as an enabling technology for future high-speed wireless networks. Full article

In this study, a polymer gel electrolyte based on polyacrylonitrile was synthesized with varying polymer-to-liquid-electrolyte ratios. DSSCs incorporating a 1:3 ratio showed optimum PV parameters. Choosing this proportion, the effect of incorporating the photoresponsive AZO dye into this polymer electrolyte was studied. When irradiated with a UV light of 365 nm, the AZO dye underwent photoisomerization, which allowed the gel electrolyte to absorb heat from the UV irradiation and increase its ionic conductivity. It was found that by the addition of azopyridine into the polymer electrolyte, there was an improvement in the photovoltaic parameters of cells. By increasing the dye content from 1% to 10% by weight in the electrolyte, an 11% growth in short current density was observed, resulting in about a 10% rise in cell efficiency. Full article

In this study, in situ piezoelectricity was incorporated into the photoactive region to prepare a self-powered deep-ultraviolet photodetector based on a mixture of polyvinylidene fluoride (PVDF)@Ga₂O₃ and polyethyleneimine (PEI)/carbon quantum dots (CQDs). A ferroelectric composite layer was prepared using β-Ga₂O₃ as a filler, and the β-phase of PVDF was used as the polymer matrix. The strong piezoelectricity of β-PVDF can facilitate the separation and transport of photogenerated carriers in the depletion region and significantly reduce the dark current when the device is biased with an external bias, resulting in a high on/off ratio and high detection capability. The self-powered PD exhibited specific detectivity (D* = 3.5 × 10¹⁰ Jones), an on/off ratio of 2.7, and a response speed of 0.11/0.33 s. Furthermore, the prepared PD exhibits excellent photoresponse stability under continuous UV light, with the photocurrent retaining 83% of its initial value after about 500 s of irradiation. Our findings suggest a new approach for developing cost-effective UV PDs for optoelectronic applications in related fields. Full article

Organic phototransistors, renowned for their exceptional biocompatibility, hold promise in phototherapy for tracking the efficacy of photosensitive drugs within treatment areas. Nevertheless, it has been found that organic semiconductors are less effective in detecting ultraviolet (UV) light because of their narrow bandgap. Here, we show that UV photodetection in phototransistors using donor-acceptor (D-A) polymer semiconductors can be significantly enhanced by incorporating PCBM nanocrystals. This integration results in a band mismatch between the nanocrystals and the D-A polymer at the interface. These nanocrystals also demonstrate a notable capability of modulating threshold voltage under UV light. The devices incorporating nanocrystals exhibit a photoresponsivity of 0.16 A/W, surpassing the photoresponsivity of the devices without nanocrystals by 50%. The specific detection rate of devices with nanocrystals is around 2.00 × 10¹⁰ Jones, which is twice as high as that of devices without nanocrystals. The presented findings offer a potential avenue to improve the efficiency of polymer phototransistors for UV detection. Full article

Using structured light to drive colloidal motors, due to its advantages of remote manipulation, energy tunability, programmability, and the controllability of spatiotemporal distribution, has been attracting much attention in the fields of targeted drug delivery, environmental control, chemical agent detection, and smart device design. Here, we focus on studying the group control of colloidal motors made from a photo-responsive organic polymer molecule NO-COP (N,O-Covalent organic polymer). These colloidal motors mainly respond to light intensity patterns. Considering its merits of fast refreshing speed, good programmability, and high-power threshold, we chose a digital micromirror device (DMD) to modulate the structured light field shining on the sample. It was found that under ultraviolet or green light modulation, such colloidal motors exhibit various group behaviors including group spreading, group patterning, and group migration. A qualitative interpretation is also provided for these observations. Full article

Shape-shifting polymers are widely used in various fields such as intelligent switches, soft robots and sensors, which require both multiple stimulus-response functions and qualified mechanical strength. In this study, a novel near-infrared-light (NIR)-responsible shape-shifting hydrogel system was designed and fabricated through embedding vinylsilane-modified carbon nanotubes (CNTs) into particle double-network (P-DN) hydrogels by micellar copolymerisation. The dispersed brittle Poly(sodium 2-acrylamido-2-methylpropane-1-sulfonate) (PNaAMPS) network of the microgels can serve as sacrificial bonds to toughen the hydrogels, and the CNTs endow it with NIR photothermal conversion ability. The results show that the CNTs embedded in the P-DN hydrogels present excellent mechanical strength, i.e., a fracture strength of 312 kPa and a fracture strain of 357%. Moreover, an asymmetric bilayer hydrogel, where the active layer contains CNTs, can achieve 0°–110° bending deformation within 10 min under NIR irradiation and can realise complex deformation movement. This study provides a theoretical and experimental basis for the design and manufacture of photoresponsive soft actuators. Full article

Carbon nitrides form a series of polymer semiconductors popular in photocatalysis. In the course of photoresponse, the separation of light-induced electron–hole pairs is one of the critical factors that affect the conversion rate from photoenergy to chemical substance. Exciton binding energy ($E_b$) is treated as a classical parameter to evaluate the barrier of exciton dissociation. In this work, we study the electronic and optical nature of two specific members of the carbon nitride family, polymeric carbon nitride (melon) and crystallized poly(triazine imide) (PTI/Li⁺Cl⁻) by employing the photoluminescence spectra and density functional theory (DFT) calculations based on the Wannier-Mott exciton module. The results of self-consistent GW computation were applied. The measurement of photoluminescence spectra, by which exciton binding energies are estimated, is likewise discussed. Generally, compared with the results calculated by GW-BSE, the DFT results based on the Wannier-Mott model are closer to the experimental values. From a materials perspective, on the other hand, the exciton binding energy of the melon is lower than that of PTI/Li⁺Cl⁻. Full article

Implantable hydrogels should ideally possess mechanical properties matched to the surrounding tissues to enable adequate mechanical function while regeneration occurs. This can be challenging, especially when degradable systems with a high water content and hydrolysable chemical bonds are required in anatomical sites under constant mechanical stimulation, e.g., a foot ulcer cavity. In these circumstances, the design of hydrogel composites is a promising strategy for providing controlled structural features and macroscopic properties over time. To explore this strategy, the synthesis of a new photocurable elastomeric polymer, poly(glycerol-co-sebacic acid-co-lactic acid-co-polyethylene glycol) acrylate (PGSLPA), is investigated, along with its processing into UV-cured hydrogels, electrospun nonwovens and fibre-reinforced variants, without the need for a high temperature curing step or the use of hazardous solvents. The mechanical properties of bioresorbable PGSLPA hydrogels were studied with and without electrospun nonwoven reinforcement and with varied layered configurations, aiming to determine the effects of the microstructure on the bulk compressive strength and elasticity. The nonwoven reinforced PGSLPA hydrogels exhibited a 60% increase in compressive strength and an 80% increase in elastic moduli compared to the fibre-free PGSLPA samples. The mechanical properties of the fibre-reinforced hydrogels could also be modulated by altering the layering arrangement of the nonwoven and hydrogel phase. The nanofibre-reinforced PGSLPA hydrogels also exhibited good elastic recovery, as evidenced by the hysteresis in compression fatigue stress–strain evaluations showing a return to the original dimensions. Full article

In recent years, there has been a growing interest in developing smart drug delivery systems based on natural resources combined with stimulus-sensitive elements. This trend aims to formulate innovative and sustainable delivery platforms tailored for topical applications. This work proposed the use of layer-by-layer (LbL) methodology to fabricate biocompatible photo-responsive multilayer systems. These systems are composed of a polyoxometalate inorganic salt (POM) ([NaP₅W₃₀O₁₁₀]¹⁴⁻) and a natural origin polymer, chitosan (CHT). Curcumin (CUR), a natural bioactive compound, was incorporated to enhance the functionality of these systems during the formation of hollow capsules. The capsules produced, with sizes between 2–5µm (SEM), were further dispersed into CHT/VCO (virgin coconut oil) emulsion solutions that were casted into molds and dried at 37 °C for 48 h. The system presented a higher water uptake in PBS than in acidic conditions, still significantly lower than that earlier reported to other CHT/VCO-based systems. The drug release profile is not significantly influenced by the medium pH reaching a maximum of 37% ± 1% after 48 h. The antioxidant performance of the designed structures was further studied, suggesting a synergistic beneficial effect resulting from CUR, POM, and VCO individual bioactivities. The increased amount of those excipients released to the media over time promoted an increase in the antioxidant activity of the system, reaching a maximum of 38.1% ± 0.1% after 48 h. This work represents a promising step towards developing advanced, sustainable drug delivery systems for topical applications. Full article

Block copolymers are a class of materials that are particularly interesting with respect to their capability to self-assemble in ordered structures. In this context, the coupling between environment and dynamics is particularly relevant given that movements at the molecular level influence various properties of macromolecules. Mixing the polymer with a second macromolecule appears to be an easy method for studying these relationships. In this work, we studied blends of poly(methyl methacrylate) (PMMA) and a block copolymer composed of PMMA as the first block and poly(3-methyl-4-[6-(methylacryloyloxy)-hexyloxy]-4′-pentyloxy azobenzene) as the second block. The relaxational properties of these blends were investigated via electron spin resonance (ESR) spectroscopy, which is sensitive to nanometric length scales. The results of the investigations on the blends were related to the dynamic behavior of the copolymers. At the nanoscale, the study revealed the presence of heterogeneities, with slow and fast dynamics available for molecular reorientation, which are further modulated by the ability of the block copolymers to form supramolecular structures. For blends, the heterogeneities at the nanoscale were still detected. However, it was observed that the presence of the PMMA as a major component of the blends modified their dynamic behavior. Full article

A highly uniform spherical MoO₂-MoO₃/polypyrrole core-shell nanocomposite has been successfully synthesized as an optoelectronic photon sensing material, capable of detecting light in the UV, Vis, and IR domains. The nanocomposite is prepared through the oxidation of pyrrole using Na₂MoO₄, resulting in a uniform spherical morphology that has been confirmed by TEM, theoretical modeling, and SEM analyses. This morphology contributes to its promising optical behavior, characterized by a small bandgap of 1.36 eV. The optoelectronic photosensing capability of the nanocomposite has been evaluated across the UV, Vis, and IR spectra, demonstrating high efficiency. The photoresponsivity R values indicate the ability of the nanocomposite to generate hot electrons in response to incident photons. With an R value of 4.15 mA·W⁻¹ at 440 nm, this optoelectronic device exhibits considerable promise for integration into an advanced technological apparatus. The detection (D) value of 9.30 × 10⁸ Jones at 440 nm further confirms the high sensitivity in the Vis region. The excellent stability of the device can be attributed to the inherent MoO₂-MoO₃ oxide and Ppy polymer materials. This stability has been demonstrated through reproducibility studies and current-voltage measurements under various optical conditions. The combination of stability, efficiency, and sensitivity makes this optoelectronic device well suited for light sensing applications in both industrial and commercial settings. Its promising performance opens up opportunities for advancements in various fields requiring accurate and reliable light detection. Full article

This study achieved the decoration of poly-3-methyl aniline (P3MA) with As₂O₃–As(OH)₃ using K₂S₂O₈ and NaAsO₂ on the 3-methyl aniline monomer. This resulted in a highly porous nanocomposite polymer composite with wide absorption optical behavior, an average crystalline size of 22 nm, and a 1.73 eV bandgap. The photoelectrode exhibited a great electrical response for electroanalytical applications, such as photon sensing and photodiodes, with a J_ph of 0.015 mA/cm² and J_o of 0.004 mA/cm². The variable J_ph values ranged from 0.015 to 0.010 mA/cm² under various monochromatic filters from 340 to 730 nm, which demonstrates high sensitivity to wavelengths. Effective photon numbers were calculated to be 8.0 × 10²¹ and 5.6 × 10²¹ photons/s for these wavelength values, and the photoresponsivity (R) values were 0.16 and 0.10 mA/W, respectively. These high sensitivities make the nanocomposite material a promising candidate for use in photodetectors and photodiodes, with potential for commercial applications in highly technological systems and devices. Additionally, the material opens up possibilities for the development of photodiodes using n- and p-type materials. Full article

Hydrogels are materials consisting of a network of hydrophilic polymers. Due to their good biocompatibility and hydrophilicity, they are widely used in biomedicine, food safety, environmental protection, agriculture, and other fields. This paper summarizes the typical complex materials of photocatalysts, photosensitizers, and hydrogels, as week as their antibacterial activities and the basic mechanisms of photothermal and photodynamic effects. In addition, the application of hydrogel-based photoresponsive materials in microbial inactivation is discussed, including the challenges faced in their application. The advantages of photosensitive antibacterial complex hydrogels are highlighted, and their application and research progress in various fields are introduced in detail. Full article