Search Results (22)

Optically responsive materials are applied in sensing, actuators, and optical devices. One such class of material is dye-doped liquid crystal polymers that self-assemble into cholesteric mesophases that reflect visible light. We report here the synthesis and characterization of a family of linear and mildly crosslinked terpolymers prepared by the ROMP of norbornene-based monomers. The three monomers were composed of (i) rhodamine dye through one or two norbornene end groups utilizing flexible C₁₀-alkane spacers, (ii) a cholesteryl liquid crystal (LC) using C₉-alkane spacers, and (iii) PEG side chains. We investigated how these architectural variations in these terpolymers impacted their hierarchically self-assembled mesophase properties. We probed their composition, morphology, thermal, mechanic, photochromic, and mechanochromic properties using, inter alia, ¹H NMR spectroscopy, DSC, temperature-dependent SAXS, diffuse reflectance UV-vis spectroscopy, and optical polarization microscopy. The new terpolymers exhibited architecture-dependent thermochromic, mechanochromic, and piezochromic properties arising from LC–rhodamine dye interactions. We found that a compromise between the rigidity and flexibility of the terpolymer architectures needed to be stricken to fully express stimuli-responsive properties. These terpolymers also showed distinctly different properties compared to those of a previously reported structurally related liquid crystalline copolymer made from two monomers. These findings help to define the design principles for optimally stimuli-responsive liquid crystalline polymers. Full article

We developed dye-sensitized solar cells (DSSCs) using 1,5-carboxy-2-[[3-[(2,3-dihydro-1,1-dimethyl-3-ethyl-1H-benzo[e]indol-2-ylidene)methyl]-2-hydroxy-4-oxo-2-cyclobuten-1-ylidene]methyl]-3,3-dimethyl-1-octyl-3H-indolium and 1,3,3-trimethyl indolino-6′-nitrobenzopyrylospiran. The DSSCs incorporate photochromic molecules to regulate photoelectric conversion properties. We irradiated photoelectrodes adsorbed with SQ2/SPNO₂ using both UV and visible light and observed the color changes in these photoelectrodes. Following UV irradiation, the transmittance at 540 nm decreased by 20%, while it increased by 15% after visible light irradiation. This indicates that SPNO₂ on the DSSCs is photoisomerized from the spiropyran form (SP) to the photomerocyanine (PMC) form under UV light. The photoelectric conversion efficiency (η) of the DSSCs increased by 0.15% following 5 min of UV irradiation and decreased by 0.07% after 5 min of visible light irradiation. However, direct electron injection from PMC seems challenging, suggesting that the mechanism for improved photoelectric conversion in these DSSCs is likely due to Förster resonance energy transfer (FRET) from PMC to the SQ2 dye. The findings suggest that the co-sensitization of DSSCs by PMC-SQ2 and SQ2 alone, facilitated by their respective photoabsorption, results in externally responsive and co-sensitized solar cells. This study provides valuable insights into the development of advanced DSSCs with externally controllable photoelectric conversion properties via the strategic use of photochromic molecules and energy transfer mechanisms, advancing future solar energy applications. Full article

The art of dyeing textiles has a long history, as natural dyes have been used since prehistoric times. With the development of synthetic dyes in the 19th century, the focus shifted from natural to synthetic dyes due to their superior properties. Recently, however, interest in natural dyes has increased again due to environmental and health concerns. Among industrial dyes, heterocyclic dyes, especially azo dyes, are of great importance due to their color brilliance and fastness. This review examines the synthesis, application, and analysis of azo dyes, especially heterocyclic dyes. It deals with monoazo, diazo, and polyazo dyes and highlights their structures, synthesis methods, and fastness properties. In addition, the ecological impact of azo dyes and practical solutions for their synthesis and application are discussed. Full article

Azo-Schiff bases contain an azo photochrome showing isomerization accompanying with color change, and an imine moiety (which can contribute to the metal complexation capability). The syntheses of these molecules will be described, and their dyes applications will be discussed, such as for fuel cells, as photometric or colorimetric sensors. In addition, liquid crystals and their antibacterial efficiencies will also be discussed. Full article

In recent years, there has been a huge surge in interest in improving the efficiency of smart electronic and optoelectronic devices via the development of novel materials and printing technologies. Inkjet printing, known to deposit ‘ink on demand’, helps to reduce the consumption of materials. Printing inks on various substrates like paper, glass, and fabric is possible, generating flexible devices that include supercapacitors, sensors, and electrochromic devices. Newer inks being tested and used include formulations of carbon nanoparticles, photochromic dyes, conducting polymers, etc. Among the conducting polymers, PANI has been well researched. It can be synthesized and doped easily and allows for the easy formation of composite conductive inks. Doping and the addition of additives like metal salts, oxidants, and halide ions tune its electrical properties. PANI has a large specific capacitance and has been researched for its applications in supercapacitors. It has been used as a sensor for pH and humidity as well as a biosensor for sweat, blood, etc. The response is generated by a change in its electrical conductivity. This review paper presents an overview of the investigations on the formulation of the inks based on conductive polymers, mainly centered around PANI, and inkjet printing of its formulations for a variety of devices, including supercapacitors, sensors, electrochromic devices, and patterning on flexible substrates. It covers their performance characteristics and also presents a future perspective on inkjet printing technology for advanced electronic, optoelectronic, and other conductive-polymer-based devices. We believe this review provides a new direction for next-generation conductive-polymer-based devices for various applications. Full article

Carbohydrate-based low-molecular-weight gelators are interesting new materials with many potential applications. These compounds can be designed to include multiple stimuli-responsive functional groups. In this study, we designed and synthesized several chemically responsive bola-glycolipids and dimeric carbohydrate- and diarylethene-based photoswitchable derivatives. The dimeric glycolipids formed stable gels in a variety of solvent systems. The best performing gelators in this series contained decanedioic and dithienylethene (DTE) spacers, which formed gels in eight and nine of the tested solvents, respectively. The two new DTE-containing esters possessed interesting photoswitching properties and DTE derivative 7 was found to have versatile gelation properties in many solvents, including DMSO solutions at low concentrations. The gels formed by these compounds were stable under acidic conditions and tended to hydrolyze under basic conditions. Several gels were used to absorb rhodamine B and Toluidine blue from aqueous solutions. In this study, we demonstrated the rational design of molecular gelators which incorporated photoresponsive and pH responsive functions, leading to the discovery of multiple effective stimuli-responsive gelators. Full article

Titanium dioxide (TiO₂) plays a pivotal role in photocatalytic reactions and holds great promise for the cosmetic and paint industries due to its white color and high refractive index. However, the original color of TiO₂ changes gradually to blue or yellow with UV irradiation, which affects its color realization. We encapsulated TiO₂ with several natural organic dye compounds, including purpurin, curcumin, and safflower, to control its photochromism and realize a range of different colors. The chemical reaction between TiO₂ and dyes based on their functional group was investigated, and the light absorption was tested via FTIR and UV–Vis spectroscopy. The changes in morphology and size distribution additionally supported their successful encapsulation. The discoloration after UV irradiation was evaluated by measuring the color difference (ΔE) of control TiO₂ and dye encapsulated TiO₂. The unique structure utilized natural dyes to preserve photochromism based on the physical barrier and automatically controlled the electronic transition of core TiO₂. In particular, the color difference values of purpurin and curcumin were 4.05 and 3.76, which is lower than the 5.36 of the control TiO₂. Dye encapsulated TiO₂ was manipulated into lipstick to verify its color realization and retention. Full article

Wood dyeing is an effective way to alleviate the supply-demand imbalance of valuable wood and improve the surface decoration of fast-growing wood. However, applications of dyed wood are limited due to the susceptibility of dyes and wood to photo-discolor and degrade under light irradiation. Thus, the improved weather resistance of dyed wood is crucial. To prevent photochromic discoloration of dyed wood, an anti-photochromic coating structure was constructed via layer-by-layer self-assembly (LbL) using chitosan and zinc oxide (ZnO). The results showed that the surface color difference of treated dyed wood was reduced by approximately 84.6% after the first 2 h of irradiation under the following conditions °C: temperature (50 °C), relative humidity (55%), and irradiation intensity (550 W/m²). However, the color of untreated dyed wood drastically changed at this stage. The reason for the decrease was that the redness and yellowness of treated dye wood were significantly reduced. The deposition of ZnO onto treated dyed wood helped to protect the wood from UV light irradiation. Chitosan bridged the dyes and complexed ZnO to enhance UV resistance. This study provides valuable information for the protection of dyed wood against light discoloration that can be used as an interior and exterior decorative material. Full article

With the development of the economy and science and technology, consumers have put forward higher requirements for the functionality of surface coatings on wood products and metal products, which requires us to endow traditional coatings with new functions. Innovative research of coatings has been a research hotspot in recent years, and the combination of microencapsulation technology with coatings is a research direction attracting much attention. In this paper, a kind of spirooxazine color-changing microcapsules containing photochromic purple dye was selected to explore the effect of different loadings of the photochromic microcapsules on the properties of the coatings. The photochromic microcapsules were added to the waterborne coating with loadings of 5.0%, 10.0%, 15.0%, 20.0% and 25.0%. The coatings were coated on Tilia europaea boards and aluminum alloy plates to explore the optical properties, mechanical properties, cold liquid resistance and aging resistance of the coatings. The results showed that the coating had good photochromic property on wood substrate and metal substrate. When the loading was 15.0% and 10.0%, the comprehensive performance of the coating was good. The color difference of the coating before and after photochromism was 51.0 and 62.0, the glossiness was 7.1% and 15.9%, the hardness was 3H, the adhesion grade was 1, the impact resistance was 4 kg·cm, the roughness was 1.2 μm and 0.9 μm and the liquid resistance grade was 1. The research results show that the photochromic microcapsule can endow the paint with a reversible color change function and improve some mechanical properties of the coating, which indicates that the composite prepared in this study can be used in the surface finishing of wood and metal and has certain research value and application potential. Full article

Six new bio-inspired flavylium salts were synthesized and investigated by a combined computational and experimental study for dye-sensitized solar cell applications. The compounds were characterized by FT–IR, UV–Vis, NMR spectroscopy, and LC–MS spectrometry techniques. The pH-dependent photochromic properties of the flavylium dyes were investigated through a UV–Vis spectroscopy study and revealed that they follow the same network of chemical reactions as anthocyanins upon pH changes. The structural and electronic properties of the dyes were investigated using density functional theory (DFT) and time-dependent density functional theory (TD–DFT). Geometry optimization calculation revealed that all dyes, regardless of the specie, flavylium cations or quinoidal bases, present a planar geometry. The photovoltaic performances of the dyes, in both flavylium and quinoidal base forms, were evaluated by the HOMO and LUMO energies and by calculating the light-harvesting efficiencies, the free energy change of electron injection, and the free energy change regeneration. The MO analysis showed that all dyes can inject electrons into the conduction band of the TiO₂ upon excitation and that the redox couple can regenerate the oxidized dyes. The results obtained for the free energy change of electron injection suggest that the quinoidal bases should inject electrons into the semiconductor more efficiently than the flavylium cations. The values for the free energy change regeneration showed that the redox electrolyte can easily regenerate all dyes. Dipole moment analysis was also performed. DSSCs based on the dyes, in both flavylium and quinoidal base forms, were assembled, and their photovoltaic performances were evaluated by measuring the open-circuit voltage, the short circuit current density, the fill factor, and the energy conversion efficiency. Results obtained by both experimental and computational studies showed that the overall performances of the DSSCs with the quinoidal forms were better than those obtained with the flavylium cations dyes. Full article

Photochromic materials have attracted increasing attention. Here, we report a novel photo-reversible color switching system based on oxygen-vacancy-engineered MoO_x nanostructures with water/N-methyl-2-pyrrolidone (NMP) as solvents. In this work, the system rapidly changed from colorless to blue under UV irradiation (360–400 nm) and slowly recovered its colorless state under visible light irradiation. The obtained oxygen vacancy-engineered MoO_x nanostructures exhibited good repeatability, chemical stability, and cycling stability. Upon UV light irradiation, H⁺ was intercalated into layered MoO_x nanostructures and the Mo⁶⁺ concentration in the H_xMoO_x decreased, while the Mo⁵⁺ concentration increased and increased oxygen vacancies changed the color to blue. Then, it recovered its original color slowly without UV light irradiation. What is more, the system was highly sensitive to UV light even on cloudy days. Compared with other reported photochromic materials, the system in this study has the advantage of facile preparation and provides new insights for the development of photochromic materials without dyes. Full article

Azobenzenes are photochromic molecules that possess a large range of applications. Their syntheses are usually simple and fast, and their purifications can be easy to perform. Oligosaccharide is also a wide family of biopolymer constituted of linear chain of saccharides. It can be extracted from biomass, as for cellulose, being the principal constituent of plant cell wall, or it can be enzymatically produced as for cyclodextrins, having properties not far from cellulose. Combining these two materials families can afford interesting applications such as controlled drug-release systems, photochromic liquid crystals, photoresponsive films or even fluorescent indicators. This review will compile the different syntheses of azo-dyes-grafted oligosaccharides, and will show their various applications. Full article

In this work, we reported a new insight on the kinetics of photoisomerization and time evolution of hybrid thin films considering the azo-dye methyl red (MR) incorporated with graphene accommodated in polyethylene oxide (PEO). The kinetics of photoisomerization and time-evolution of hybrid thin films were investigated using UV-Vis s and FTIR spectroscopies, as well as appropriate models developed with new analytical methods. The existence of azo-dye MR in the complex is crucial for the resource action of the trans$\leftrightarrow$cis cycles through UV-illumination $\leftrightarrow$ Visible-illumination relaxations. The results of the UV–Vis and the FTIR investigations prove the cyclical trans$\leftrightarrow$cis-states. Consequently, PEO-(MR-Graphene) hybrid composite thin films can be introduced as possible applicants for photochromic molecular switches, light-gated transistors, and molecular solar thermal energy storage media. Full article

Dimming and scattering control are two of the major features of smart windows, which provide adjustable sunlight intensity and protect the privacy of people in a building. A hybrid photo- and electrical-controllable smart window that exploits salt and photochromic dichroic dye-doped cholesteric liquid crystal was developed. The photochromic dichroic dye causes a change in transmittance from high to low upon exposure to sunlight. When the light source is removed, the smart window returns from colored to colorless. The salt-doped cholesteric liquid crystal can be bi-stably switched from transparent into the scattering state by a low-frequency voltage pulse and switched back to its transparent state by a high-frequency voltage pulse. In its operating mode, an LC smart window can be passively dimmed by sunlight and the haze can be actively controlled by applying an electrical field to it; it therefore exhibits four optical states—transparent, scattering, dark clear, and dark opaque. Each state is stable in the absence of an applied voltage. This smart window can automatically dim when the sunlight gets stronger, and according to user needs, actively adjust the haze to achieve privacy protection. Full article

We present investigation of optical and photochromic properties as well as of surface quality of thin films of novel methacrylic polymers with 8-hydroxyquinoline azo-dyes in side-chain. Additionally, thermal stability of polymer powders was examined and their glass transition temperature was determined. Optical properties (extinction coefficient and refractive index) were determined by spectroscopic ellipsometry (SE) combined with absorbance measurements. Photoresponsive behavior was investigated by determination of photoisomerization rates under irradiation with unpolarized 365 nm light, as well as by conduction of holographic grating inscription experiment. Thin film quality was determined by atomic force microscopy (AFM) measurements. Thermal analysis was performed by thermogravimetric (TG), derivative thermogravimetric (DTG) and differential scanning calorimetry (DSC) measurements. We found that optical properties as well as photoisomerization rates of investigated polymers are dependent on the substituent in the para position of the phenyl ring. Surface relief grating inscription was successfully generated only for materials with chromophores containing dimethylamino (N(CH₃)₂) and methyl (CH₃) substituents, but all materials exhibited birefringence grating in the bulk. Surface of most thin films was very smooth, but its quality was impaired by neutral (H) as well as carboxyl (COOH) substituent. Thermal stability of copolymers with side-chain chromophores was improved compared to pure poly(methyl methacrylate) (PMMA). Full article