A Modified Oxazolone Dye Dedicated to Spectroscopy and Optoelectronics.

Here we present a newly synthesized bifunctional organic chromophore with appealing spectroscopic and nonlinear optical features. The positions of absorption and emission maxima of the dye vary with increasing solvent polarity and exhibit positive solvatochromism. The determined change in the dipole moment upon excitation based on the Bilot and Kawski theory is 5.94 D, which corresponds to the intermolecular displacement of a charge equal to 1.24 Å. An investigated organic-based system represents a significant, repeatable, and stable over time optical signal modulation in the manner of the refractive index value. Its magnitude is varied both by optical pumping intensity as well as by external frequency modulation, which indicates that such system is an alluring and alternative core unit for optoelectronic devices and complex networks. Then, the same active system, due to the nonresonant mechanism of higher harmonics of light inducement, can provide second and third harmonic signals. According to the introduced laser line spatial modifications (parallel or perpendicular polarization directions), it is resulted in output SHG signal with magnitude varied about 100%. Its magnitude is noticeably small; however, to construct sensitive optical sensors or infrared indicators, such feature may guarantee satisfying circumstances.

Multifunctional Oxazolone Derivative as an Optical Amplifier, Generator, and Modulator.

An optical control of many working optoelectronic systems (real-time sensors, optical modulators, light amplifiers, or phase retarders) giving efficient optical gain or remote signal modulation is currently included as scientifically and industrially interesting. In here, an oxazolone derivative as the multifunctional organic system is given in this contribution. The molecule possesses a stilbene group and an oxazolone heteroatomic ring, which implies effective refractive index manipulation and multimode lasing action, respectively. The light modulation is repeatable and stable, also in the hundreds of Hz regime. On the other hand, the amplified optical signal can be easily generated by an external optical pumping source. Thus, signal control is fully available, as is read-in and read-out of the information in real time. Furthermore, this third-order, nonlinear, optical phenomenon using a third harmonic generation technique was also observed. We discovered that only by changing the energy and time regime of the supplied optical signal is the optical or nonlinear optical response observed. Two heteroenergetic molecular states (trans (E) and cis (Z)) can efficiently operate in modern multifunctional optoelectronic systems, which can provide and generate an optical signal. Such functionalities are commonly used in all-optical photonic switchers and logic gates and can be utilized in optical-core networks and computers.

Perylene-Based Chromophore as a Versatile Dye for Light Amplification.

One of the challenges for modern optoelectronics is to find versatile, easily adaptable components for novel laser-based technologies. A very attractive perylene-derivative chromophore in different organic matrices for high-performance light amplification is discussed and outlined. Our approach demonstrates the outstandingly compatible laser dye and a viable strategy to provide an effective optical gain for stimulated emission enhancement. Through structural control, we produce simple optical devices embedded in organic matrices, such as poly(methyl methacrylate), nematic liquid crystalline (NLC) mixture, and a hybrid emulsion system (poly(vinyl alcohol) PVA + NLC mesophase). Importantly, we investigate and compare the spectroscopy of differently constructed organic systems in terms of stimulated-emission thresholds and light amplification process efficiency. Moreover, we report the effects of tunability for LC cells by an applied external electric field stimulus. Future directions of laser systems are outlined with an emphasis on the role of the perylene derivative. The studies meet current challenges in the field of modern organic technologies dedicated to various optoelectronic systems, including touch screens, displays, and Li-Fi networks.

Compatible Photochromic Systems for Opto-electronic Applications.

Today, a lot of attention is paid to remote controlled opto-electronic devices. Many of them are commonly used in the society, industry, and science. Accessories dedicated to the particular utilization are desired. The point is to find a simple way to obtain smart and functional appliances. Materials engineering faces such problems and provides a variety of solutions concerning advanced material design, preparation, and utilization. Photochromic materials represent one of the already known materials, which still find other objectives in new fields of life. In our work, we present two differently constructed photoresponsive polymers, which give significantly different nonlinear optical (NLO) response visible as noticeable optical signal modulation. By playing with diversified laser light energy or its frequency, NLO output characterized appealing, and individual characteristics (doubled Δn ∼0.02 vs 0.04 and entirely different kinetics for two similar materials and the same laser pumping). Interestingly, high output signal repeatability and stability were achieved, which indicate the investigated materials as promising candidates in the construction of various opto-electronic devices. Additionally, a set of photoresponsive studies, reflectometry, and theoretical insights was performed and included in this work.

Triboluminescence Phenomenon Based on the Metal Complex Compounds-A Short Review.

Triboluminescence (TL) is a phenomenon of light emission resulting from the mechanical force applied to a substance. Although TL has been observed for many ages, the radiation mechanism is still under investigation. One of the exemplary compounds which possesses triboluminescent properties are copper(I) thiocyanate bipyridine triphenylphosphine complex [Cu(NCS)(py)2(PPh3)], europium tetrakis dibenzoylmethide triethylammonium EuD4TEA, tris(bipyridine)ruthenium(II) chloride [Ru(bpy)3]Cl2, and bis(triphenylphosphine oxide)manganese(II) bromide Mn(Ph3PO)2Br2. Due to the effortless synthesis route and distinct photo- and triboluminescent properties, these compounds may be useful model substances for the research on the triboluminescence mechanism. The advance of TL studies may lead to the development of a new group of sensors based on force-responsive (mechanical stimuli) materials. This review constitutes a comprehensive theoretical study containing available information about the coordination of metal complex synthesis methodologies with their physical, chemical, and spectroscopic properties.

Dye Stabilization and Wavelength Tunability in Lasing Fibers Based on DNA.

Lasers based on biological materials are attracting an increasing interest in view of their use in integrated and transient photonics. Deoxyribonucleic acid (DNA) as optical biopolymer in combination with highly emissive dyes has been reported to have excellent potential in this respect. However, achieving miniaturized lasing systems based on solid-state DNA shaped in different geometries to confine and enhance emission is still a challenge, and the physicochemical mechanisms originating fluorescence enhancement are not fully understood. Herein, a class of wavelength-tunable lasers based on DNA nanofibers is demonstrated, for which optical properties are highly controlled through the system morphology. A synergistic effect is highlighted at the basis of lasing action. Through a quantum chemical investigation, it is shown that the interaction of DNA with the encapsulated dye leads to hindered twisting and suppressed channels for the nonradiative decay. This is combined with effective waveguiding, optical gain, and tailored mode confinement to promote morphologically controlled lasing in DNA-based nanofibers. The results establish design rules for the development of bright and tunable nanolasers and optical networks based on DNA nanostructures.

Photoactivated Refractive Index Anisotropy in Fluorescent Thiophene Derivatives.

The optical control of anisotropy in materials is highly advantageous for many technological applications, including the real-time modulation of another light signal in photonic switches and sensors. Here, we introduce three thiophene derivatives with a donor-acceptor structure, which feature different positions of an electron-acceptor nitrile group, and both photoalignment and luminescence properties. Quantum chemical calculations highlight the presence of trans-forms stable at room temperature and metastable cis-isomers. Besides photoluminescence peaked at 440-460 nm and 0.4 ns lifetime, the three nonlinear optical chromophores exhibit photoinduced anisotropy of the refractive index closely depending on the specific molecular structure, with higher values of birefringence at lower driving signal being obtained for ortho substitution of the nitrile group. All-optical modulation of an external light beam at rates of hundreds of hertz is demonstrated in the fluorescent systems. This finding opens an interesting route to multispectral photonic switches embedded in the active layers of light-emitting devices.

Electrically controlled white laser emission through liquid crystal/polymer multiphases.

White lasers are becoming increasingly relevant in various fields since they exhibit unprecedented properties in terms of beam brightness and intensity modulation. Here we introduce a white laser based on a polymer matrix encompassing liquid crystals and multiple organic chromophores in a multifunctional phase-separation system. The separation of the hydrophilic matrix and the hydrophobic liquid crystals leads to the formation of a complex optically active layer, featuring lasing emission tuneable from blue to red. White laser emission is found with an optical excitation threshold of approximately 12 mJ/cm2. Importantly, an external electric field can be used to control the device emission intensity. White lasers with low-voltage (≤10 V) controllable emission might pave the way for a new generation of broadband light sources for analytical, computational, and communication applications.

All-optical switching in dye-doped DNA nanofibers.

All-optical switches are introduced which are based on deoxyribonucleic acid (DNA) in the form of electrospun fibers, where DNA is semi-intercalated with a push-pull, luminescent nonlinear pyrazoline derivative. Optical birefringence is found in the organic nanofibers, with fully reversible switching controlled through continuous-wave laser irradiation. The photoinduced signal is remarkably large, with birefringence highlighted by optically-driven refractive index anisotropy approaching 0.001. Sub-millisecond characteristic switching times are found. Integrating dye-intercalated DNA complex systems in organic nanofibers, as a convenient and efficient approach to template molecular organization and control it by external stimuli, might open new routes for realizing optical logic gates, reconfigurable photonic networks and sensors through physically-transient biopolymer components.

Low-Molecular Push-Pull Pyrazoline Derivatives: Solvatochromic Effect and Theoretical Insights into Dye-based Molecular Engineering.

Intermolecular interactions between dyes and solvents are essential in understanding a number of phenomena. In this contribution, we focused on similarities and differences between two molecules belonging to the same pyrazoline derivatives group: the small and rigid- 3-(1,1-dicyanoethenyl)-1-phenyl-4,5-dihydro-1 H-pyrazole (DCNP) molecule and the quite long and flexible one of (4-(2-(1-phenyl-4,5-dihydro-1 H-pyrazol-3-yl)vinyl)benzylidene) malononitrile (PY-PhdiCN). We experimentally show and use theoretical calculations to prove that extension of π-connector significantly changes the electrostatic potential distribution, which results in delocalization of negative charge along the whole donor group and increases potential surface of interaction with solvent molecules giving large spectral shifts. We also show that pyrazoline derivatives are very effective and sensitive solvent indicators with long-time stability.

All-Optical Switching and Two-States Light-Controlled Coherent-Incoherent Random Lasing in a Thiophene-Based Donor-Acceptor System.

We describe herein the synthesis and characterization of a thiophene-based donor-acceptor system, namely (E)-2-(4-nitrostyryl)-5-phenylthiophene (Th-pNO2 ), which was prepared under Horner-Wadsworth-Emmons conditions. The UV/Vis absorption bands, including the intramolecular charge transfer (ICT) band, were fully assigned using DFT and TD-DFT computations. The results of both efficient third-order nonlinear optical properties and light-amplification phenomena are presented. Investigations of photoinduced birefringence (PIB) in optical Kerr effect (OKE) experiments showed a great potential for this particular compound as an efficient, fully reversible, and fast optical switch. Time constants for the observed trans-cis-trans molecular transitions are in the range of microseconds and give a competitive experimental result for the well-known and exploited azobenzene derivatives. Random lasing (RL) investigations confirmed that this organic system is potentially useful to achieve strong light enhancement, observed as a multimode lasing action. Both RL and OKE measurements indicate that this material is a representative of thiophene derivatives, which can be utilized to fabricate fast all-optical switches or random lasers (light amplifiers).

Physically transient photonics: random versus distributed feedback lasing based on nanoimprinted DNA.

Room-temperature nanoimprinted, DNA-based distributed feedback (DFB) laser operation at 605 nm is reported. The laser is made of a pure DNA host matrix doped with gain dyes. At high excitation densities, the emission of the untextured dye-doped DNA films is characterized by a broad emission peak with an overall line width of 12 nm and superimposed narrow peaks, characteristic of random lasing. Moreover, direct patterning of the DNA films is demonstrated with a resolution down to 100 nm, enabling the realization of both surface-emitting and edge-emitting DFB lasers with a typical line width of <0.3 nm. The resulting emission is polarized, with a ratio between the TE- and TM-polarized intensities exceeding 30. In addition, the nanopatterned devices dissolve in water within less than 2 min. These results demonstrate the possibility of realizing various physically transient nanophotonics and laser architectures, including random lasing and nanoimprinted devices, based on natural biopolymers.