Nonlinear refraction and photoinduced birefringence in chlorophosphonazo I doped polymer thin films

The nonlinear refraction and photoinduced birefringence of chlorophosphonazo I (CPA I ) doped PVA thin films were investigated. The single-beam Z-scan measurement showed that CPA I doped PVA thin film possessed a large value of nonlinear refractive index (n₂=1.82×10⁻¹² cm²/W) under a pulse 532 nm excitation, and the mechanism accounting for the process of nonlinear refraction was discussed in term of resonant electronic effect. Moreover, fast and stable molecular reorientation was observed when investigating the photoinduced birefringence of CPA I doped PVA thin film with a CW 532 nm laser as pump light and a CW 650 nm laser as probe light.     

Z-scan determination of third-order nonlinear optical nonlinearity of three azobenzenes doped polymer films

The third-order nonlinear response of methyl red (MR), methyl orange (MO) and p-dimethylamino benzene arsenic acid (PDBAA) doped polyvinyl alcohol (PVA) films are studied by using the Z-scan technique under 532 nm and 1064 nm excitations. The larger third-order nonlinear refractive index of PDBAA doped PVA film is discussed in terms of fall of the energy level in excited state for the effect of heavy-atom arsenic. At the end, the second hyperpolarizabilities of the films are estimated and the figures of merit are evaluated for their value of applications in ultra-fast all-optical devices.     

Investigations on Fe doped polyvinyl alcohol films with and without gamma (γ)-irradiation

This paper deals with the preparation of pure and ferric chloride (FeCl₃) doped polyvinyl alcohol (PVA) films by solution casting method. Optical and electrical properties were systematically investigated. We have found the decrease in optical band gap energy of PVA films on doping FeCl₃. The optical band gap energy values in the present work are found to be 3.10 eV for pure PVA, 2 eV for PVA:Fe³⁺ (5 mol%), 1.91 eV for PVA:Fe³⁺(15 mol%) and 1.8 eV for PVA:Fe³⁺(25 mol%). Direct current electrical conductivity (σ) of pure, FeCl₃ doped PVA films in the temperature range 70-127 °C has been studied. At 387 K dc electrical conductivity of pure PVA film is 5.5795 μ Ω⁻¹ cm⁻¹, PVA:Fe³⁺ (5 mol%) film is 10.0936 μ Ω⁻¹ cm⁻¹ and γ-Irradiated PVA:Fe³⁺ (5 mol%) film for 900 CGY/min is 22.1950 μ Ω⁻¹ cm⁻¹. The result reveals the enhancement of the electrical conductivity with γ-irradiation. FT-IR study signifies the intermolecular hydrogen bonding between Fe³⁺ ions of FeCl₃ with OH group of PVA.     

Electro-optical characteristics of photoinduced isomerization in 2,2′-azobis[5,6-bis(dodecyloxy)quinoxaline]-azo-dye-doped nematic liquid crystals

The formation of photoinduced gratings was realized and dielectric properties were investigated in a nematic liquid crystal (LC) doped by 2,2′-azobis[5,6-bis(dodecyloxy)quinoxaline] azo dye (AD). The enhancement of the optical and electrical properties of the system was studied by dielectric spectroscopy and diffraction grating measurements. We report the electro-optical properties of LC cells containing pure LC (E7) and its doped form with 1% (wt/wt) 2,2′-azobis[5,6-bis(dodecyloxy)quinoxaline] AD. Diffraction efficiencies, η, of 441 nm pump and 632 nm probe beams were measured in two-wave-mixing experiment. Diffraction efficiency has a noteworthy increase in AD-doped nematic liquid crytals. A maximum diffraction efficiency of 14% was found for cell doped with AD, while cells without AD had a maximum efficiency of 1%. Photoinduced refractive index change Δn and nonlinear index coefficient n₂ were also determined by the two-wave-mixing method. The dielectric parameters of AD-doped E7 and pure E7 LC have been investigated in the frequency range 1 kHz-1 MHz by the dielectric-spectroscopy method. Dielectric anisotropy (Δε) property of the LCs changes from the positive type to negative type and dielectric anisotropy values decrease with AD.     

Removal of microbial biofilm on Water Hyacinth plants roots by ultrasonic treatment

The capacity of floating aquatic plants to purify sewage effluents drops rapidly as a result of biofouling processes that occur on the plant roots. This is due to the high concentration of microorganisms (MO) present in the wastewater. The possibility to apply low frequency (20 kHz) in sonification was examined under laboratory conditions. The ability of US to remove MO from the roots was studied using commercially available sonicators at intensity levels ranging from 2.7 W/cm² to 81.4 W/cm², (corresponding power levels ranging from 75 W to 500 W) while varying application periods between 5 and 60 min.The results show that MO can be removed effectively (up to 98%) by exposing the Eichhornia crassipes roots to US for 5 min at the intensity level of 64.5 W/cm². The efficiency of the wastewater treatment increased with exposure time and power input. The study proved that the US treatment is effective in removing MO that otherwise adhere to the roots, by more then two orders of magnitude.     

Birefringent azopolymer long period fiber gratings induced by 532 nm polarized laser

Based on the photoinduced birefringence in azo materials, the model of the birefringent long period fiber gratings (BLPFGs) has been proposed and the transmission of such birefringent fiber gratings was further simulated by the coupled mode theory. In order to obtain the optimum condition for making birefringent azopolymer optical fiber (APOF) gratings the photoinduced birefringence of azo dye and methyl methacrylate (MMA) copolymers was systematically studied. After photosensitivity study of azo samples, using Teflon technique, azo dye containing single mode polymer optical fiber (POF) was fabricated. Finally, BLPFGs can be fabricated in azopolymer fiber using polarized 532 nm laser. A 120 μm LPFG with a 50% duty cycle has been successfully written within the core of the fiber with 532 nm laser by an amplitude mask method. Under polarized microphotography, the grating was observed when the optical axis was set at 45° with the direction of the first polarizing lens of the polarization microscope.     

The tribological chemistry of polysulfides in mineral oil and synthetic diester

Two organic polysulfides, dipropyl trisulfide (DPTS) and 3,5-diisopropyl-1,2,4-trithiolane (DIPTT) in mineral oil (MO) and synthetic diester (DE) were investigated on thermal films and tribofilms by using X-ray absorption near edge structure (XANES) spectroscopy. The results of surface analysis reveal that the thermal films formed from MO for two additives are consist of sulfate and sulfite, while the distinct composition of the films from DE implies the different sensitivity to oxygen between two compounds. As to the tribofilms, “hydrosulfite-like compound” is differentiated from sulfite and FeS_x (1 < x < 2) is detected in low energy region from DPTS/MO, as well as a lower concentration of DPTS/DE. At a high concentration in DE, the surface of sample for DPTS is full of iron sulfide. With regard to DIPTT, iron sulfite is the exclusive oxidized form of sulfur instead of “hydrosulfite-like compound” in the tribofilms, which is an evidence suggesting a mechanism involving a role played by a thiyl radical.     

Nonlinear optical properties and photoinduced anisotropy of an azobenzene ionic liquid-crystalline polymer

The nonlinear optical properties and photoinduced anisotropy of an azobenzene ionic liquid-crystalline polymer were investigated. The single beam Z-scan measurement showed the polymer film possessed a value of nonlinear refractive index n₂ = −1.07 × 10⁻⁹ cm²/W under a picosecond 532 nm excitation. Photoinduced anisotropy in the polymer was studied through dichroism and photoinduced birefringence. A photoinduced birefringence value Δn ∼ 10⁻² was achieved in the polymer film. The mechanism for the nonlinear optical response and the physical process of photoinduced anisotropy in the polymer were discussed.     

Photoinduced effect in Ga-Ge-S based thin films

Glassy films of Ga₁₀Ge₂₅S₆₅ with 4 μm thickness were deposited on quartz substrates by electron beam evaporation. Photoexpansion (PE) (photoinduced increase in volume) and photobleaching (PB) (blue shift of the bandgap) effects have been examined. The exposed areas have been analyzed using perfilometer and an expansion of 1.7 μm (ΔV/V ≈ 30%) is observed for composition Ga₁₀Ge₂₅S₆₅ exposed during 180 min and 3 mW/cm² power density. The optical absorption edge measured for the film Ge₂₅Ga₁₀S₆₅ above and below the bandgap show that the blue shift of the gap by below bandgap photon illumination is considerable higher (ΔE_g = 440 meV) than ΔE_g induced by above bandgap illumination (ΔE_g = 190 meV). The distribution of the refraction index profile showed a negative change of the refraction index in the irradiated samples (Δn = −0.6). The morphology was examined using a scanning electron microscopy (SEM). The chemical compositions measured using an energy dispersive analyzer (EDX) indicate an increase of the oxygen atoms into the irradiated area. Using a Lloyd's mirror setup for continuous wave holography it was possible to record holographic gratings using the photoinduced effects that occur in them. Diffraction efficiency up to 25% was achieved for the recorded gratings and atomic force microscopy images are presented.     

Surface properties of UV-irradiated poly(vinyl alcohol) films containing small amount of collagen

The surface properties of poly(vinyl alcohol) (PVA) films in the presence of 1%, 3% and 5% of collagen before and after UV-irradiation have been studied by atomic force microscopy (AFM) and by contact angle measurements. PVA films have been obtained by solvent evaporation from water solution of PVA and PVA containing small amount of collagen. After drying, the samples were irradiated with UV light wavelength λ = 254 nm in air. Surface properties before and after UV-irradiation were observed using AFM. Contact angles of two liquids: diiodomethane (D) and glycerol (G) on polymeric films were measured at constant temperature using goniometer.The results have shown that the contact angle and the surface free energy for PVA films were altered by UV-irradiation. These alterations indicate photooxidation and an increase of polarity of the surface. The comparison of surface properties of PVA films and PVA containing collagen points out that collagen is more sensitive to photooxidation than PVA and PVA/collagen blends. PVA films containing collagen easier undergo photooxidation process with formation of new polar groups than pure PVA films.     

Preparation, characterization and visible-light photocatalytic activity of AgI/AgCl/TiO2

In this paper, a novel composite photocatalyst AgI/AgCl/TiO₂ was prepared by ion exchange method and characterized by XRD, SEM and UV-Vis spectrometry. The as-prepared AgI/AgCl/TiO₂ composites show much higher photocatalytic activity than AgCl/TiO₂ and AgI/TiO₂ under visible-light irradiation (λ > 400 nm) in the process of methyl orange (MO) degradation. When the molar percentage of AgI to initial AgCl is 20% (sample SE-20%), the maximal degradation efficiency of MO has reached 85.8% after irradiation for 120 min. The enhancement of photocatalytic activity of the composite photocatalyst AgI/AgCl/TiO₂ will be attributed to its good absorption in the visible-light region, especially low recombination rate of the electron-hole pairs based on the photoluminescence (PL) spectra investigation of AgI/AgCl/TiO₂ and the matching band structures of AgI, AgCl and TiO₂. The detection of reactive species by radical scavengers displays that O₂⁻ and H₂O₂ are the main reactive species for the degradation of MO under visible-light irradiation. Moreover, PL analysis by using terephthalic acid (TA) as a probe molecule further reveals that OH can be negligible for the degradation of MO.     

Third-order resonant optical nonlinearity from trans–cis photoisomerization of an azo dye in a rigid matrix

 We investigated the trans–cis photoisomerization of an azo dye in a rigid matrix and the resulting third-order resonant optical nonlinearity by means of the simple theoretical prediction of a two-energy-level system, thin-layer chromatography and H-NMR studies. A methylorange (MO), a methylred (MR), congored (CR) or a Disperse Red 1 (DR1) doped polyvinyl alcohol (PVA) or silica film was used as nonlinear optical material. The existence of equi-absorbing points, or isosbestic points in the absorbance spectrum change and the remarkable stationary transmittance to be independent of the action beam intensity enabled us to confirm the photoisomerization even in a rigid matrix. Then, we measured the third-order resonant optical nonlinearity of dichroism through the polarization absorbance spectrum measurement and determined the characteristic optical parameters of the photoisomerization in the film such as the quantum yields φ_T, φ_C, the thermal reaction constant K and the photoisomerization time constant by fitting the theoretical curve of the two-energy-level system to the observed temporal transmittance change after the action beam exposure of the MO/PVA film. The quantum yields were φˉ_T=0.36 and φˉ_C=0.38, respectively. The photoisomerization time constant of MO embedded in the PVA film was a few seconds. The thermal reaction constant K depended on the excitation beam intensity. Received: 20 June 1996/Revised version: 4 October 1996     

甲基橙偶氮染料掺杂聚乙烯醇薄膜的光存储特性研究

研究了甲基橙(MO)偶氮染料掺杂聚乙烯醇(PVA)薄膜的光致双折射和全息光存储特性.利用YAG激光二倍频(532nm)作为写入光,He-Ne激光(632.8nm)作为读出光,考察了不同染料浓度薄膜的光致双折射,探讨了光致双折射和泵浦光功率的关系,并实现了全息光存储.阐明了MO/PVA光存储的物理机制.     

Photooxidation of different organic dyes (RB, MO, TB, and BG) using Fe(III)-doped TiO2 nanophotocatalyst prepared by novel chemical method

The nano-structured Fe(III)-doped TiO₂ photocatalysts with anatase phase have been developed for the oxidation of non-biodegradable different organic dyes like methyl orange (MO), rhodamine B (RB), thymol blue (TB) and bromocresol green (BG) using UV-Hg-lamp. The different compositions of Fe_xTi_1−xO₂ (x = 0.005, 0.01, 0.05, and 0.1) nanocatalysts synthesized by chemical method (CM), have been characterized by X-ray diffraction (XRD), UV-vis diffuse reflectance spectra, specific surface area (BET), transmission electronic microscopy (TEM) analysis, XPS, ESR and zeta potential. From XRD analysis, the results indicate that all the compositions of Fe(III) doped in TiO₂ catalysts gives only anatase phase not rutile phase. For complete degradation of all the solutions of the dyes (MO, RB, TB, and BG), the composition with x = 0.005 is more photoactive compared all other compositions of Fe_xTi_1−xO₂, and degussa P25. The decolorization rate of different dyes decreases as Fe(III) concentration in TiO₂ increases. The energy band gap of Fe(III)-doped TiO₂ is found to be 2.38 eV. The oxidation state of iron has been found to be 3+ from XPS and ESR show that Fe³⁺ is in low spin state.     

Photoinduced second-order optical susceptibilities of Er2O3 doped TeO2-GeO2-PbO glasses

Second-order optical susceptibilities were established in the optically poled erbium doped tellurite glasses near the melting temperature. The non-linear optical susceptibility was formed by bicolor coherent optical treatment performed by two coherent laser beams originated from 50 ps Nd-YAG laser (λ = 1.32 μm) exciting the high pressure hydrogen laser cell emitting at 1907 nm. The non-centrosymmetric grating of the medium was created by coherent superposition of the fundamental laser illumination at 1907 nm and the doubled frequency one at 953.5 nm. The maximally all-optically poled SHG occurs for 2% doped Er₂O₃ (in weighting units) TeO₂-GeO₂-PbO glass. It was found that the photoinduced SHG demonstrates a saturation during the photo-treatment of 9-10 min using the two beams polarized at angle about 45° between them. During the coherent bicolor optical treatment it was achieved the value of second-order susceptibility up to 3.6 pm/V at 1907 nm. The optimal ratio between the fundamental beam with power density about 1.1 GW/cm² and writing doubled frequency seeding beam about 0.015 GW/cm² corresponds to the maximal of photoinduced SHG. For glasses with lower concentration of Er₂O₃, the relaxation of the second-order optical susceptibility is substantially longer and achieves SHG value that corresponds to 80% of the maximal ones. It is necessary to emphasize that efficient optically-poled grating exists only within the narrow temperature range near the glassing temperature. Possible physical mechanisms of the phenomenon observed are discussed. Generally the used glasses possess better parameters than early investigated germinate glasses.     

χ polarization induced in molecular glass of conjugated compound by all-optical poling

The paper presents the first report on χ⁽²⁾ polarization induced in molecular glass of conjugated compound by all-optical poling. Transparent thin film of molecular glass of 1,4-bis[2-[4-[N,N-di(p-tolyl)amino]phenyl]vinyl]benzene (BTAPVB) was prepared using a spin-cast technique. Dipolar as well as octupolar components in BTAPVB contributed to the formation of photoinduced χ⁽²⁾ polarization. Growth rate of χ⁽²⁾ polarization has good linear relation with E_ω⁴E_2ω, which suggested that the simultaneous processes of two-photon (ω + 2ω) and three-photon (ω + ω + ω) excitation on the same electronic level contributed to the formation of photoinduced χ⁽²⁾ polarization.     

Surface structures of K on Mo(1 1 0) surface investigated by RHEED

Phase transitions of K on Mo(1 1 0) have been studied by RHEED technique. As Ba and Cs structures on the bcc(1 1 0) surface, surface structures of K were hexagonal from RT to 250 °C for θ > 0.9 ML. The hexagonal structure successively expanded from α to γ structure with Nishiyama-Wassermamm (N-W) orientation relationship. The nearest neighbor spacing in the α structure at RT was 4.50 Å, which is very closed to the atomic distance of K in metal, and stretched to 5.14 Å in the γ structure at T = 200 °C. At temperatures greater than T = 250 °C, the γ structure oriented in N-W and Kurdjumov-Sachs (K-S) relationships at the same time and stayed up to the temperature of 450 °C. These two orientations of γ structure also appeared in all temperature range for 0.4 < θ < 0.9 ML.     

Highly sensitive reversible light-driven switches based on LaSrAlO4 single crystals

An enhanced photoinduced reversible switching of LaSrAlO₄ single crystal was investigated as a highly sensitive photoswitch. The LaSrAlO₄ crystal showed an enhanced reversible photoswitching performance with high on/off ratio of 66 at bias voltage V_b = 30 V. A linear relationship was obtained to the on/off ratio as a function of bias voltage without any saturation trend from − 30-30 V. Compared with other complicated methods, the mechanism of electric field tunable would be the simplest and possibly the most direct way to develop the optoelectronic performances.     

The effect of PVA (Bi2O3-doped) interfacial layer and series resistance on electrical characteristics of Au/n-Si (110) Schottky barrier diodes (SBDs)

Two types of Schottky Barrier Diodes (SBDs) with and without PVA (Bi₂O₃-doped) polymeric interfacial layer, were fabricated and measured at room temperature in order to investigate the effects of the PVA (Bi₂O₃-doped) interfacial layer on the main electrical parameters such as the ideality factor (n), zero-bias barrier height (Φ_B0), series resistance (R_s) and interface-state density (N_ss). Electrical parameters of these two diodes were calculated from the current-voltage (I-V) characteristics and compared with each other. The values of Φ_B0, n and R_s for SBDs without polymeric interfacial layer are 0.71 eV, 1.44 and 4775 Ω, respectively. The values of Φ_B0, n and R_s for SBDs with PVA (Bi₂O₃-doped) polymeric interfacial layer are 0.74 eV, 3.49 and 10,030 Ω, respectively. For two SBDs, the energy density distribution profiles of interface states (N_ss) were obtained from forward-bias I-V measurements by taking the bias dependence of R_s of these devices into account. The values of N_ss obtained for the SBD with PVA (Bi₂O₃-doped) polymeric interfacial layer are smaller than those of the SBD without polymeric interfacial layer.     

Air plasma or UV-irradiation applied to surface modification of pectin/poly(vinyl alcohol) blends

Poly(vinyl alcohol), pectin and their blends with different components ratio were exposed to low-temperature air plasma or high energy UV-irradiation (λ = 254 nm) for the purpose of surface modification. The physico-chemical changes in surface properties have been studied by attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR) and contact angle measurements. Surface free energy of polymeric films, its polar and dispersive components have been calculated by Owens-Wendt method. Moreover, the work of adhesion was estimated and the recovery of hydrophobic properties of modified films after storage have been also studied.The few seconds air-plasma treatment caused more effective surface modification than 5-6 h UV-irradiation. The observed changes were partially reversible, contrary to these caused by photo-modification.It was found that pectin/PVA (50:50) blend was characterised by larger susceptibility to plasma modification compared to pure pectin and pure PVA, whereas the photosensitivity to radiation of 254 nm wavelength was the lowest for this specimen in comparison to other studied samples.