Effect of guided resonance modes on emission from GaN core–shell nanorod arrays

We model the process of incoherent emission from \(\hbox {In}_{x}\hbox {Ga}_{1-x}\hbox {N/GaN}\) quantum wells in GaN core–shell nanorod arrays using finite-difference time-domain simulations. We find that high-intensity features in the emitted field correspond to guided resonance modes near the \(\varGamma \) -point of the photonic band structure. We identify one \(\varGamma \) -point mode whose electric field intensity profile is ideal for core–shell nanorod array geometries. Using this mode, we are able to simultaneously enhance the radiative recombination rate and extraction efficiency relative to an in-filled slab. We determine the conditions on radiative and nonradiative recombination rates for which the nanorod array has a higher internal and external quantum efficiency than a reference slab. We present one nanorod array geometry where the external quantum efficiency is enhanced up to a factor of 25.     

Optical properties of ZnO nanocrystals embedded in PMMA

We report in this work the preparation of thin films of ZnO nanocrystals synthesized and dispersed in polymethylmethacrylate using a easy route and deposited in class substrate by spin coating technique. Their structural and optical properties were investigated by X-ray, absorption and photoluminescence spectroscopy. The XRD patterns exhibit sharp peaks at $2\uptheta $ corresponding to the hexagonal (wurtzite) phase diffraction planes. The optically characterization, exhibit a wide absorption band in the range of the study and a large emission band with three peaks at 481.5, 531.09 and at 671.28 nm.The crystallites radius (R) was estimated by applying the effective mass approximation model and was about 1.8 nm. From measurements of second order susceptibilities using harmonic generation technique at $\lambda = 1,064\,\text{ nm }$ in picoseconds regime we deduced $\lambda _\mathrm{eff}^{<2>}$ equal to $5.95\times 10^{-10}$  m/V. Obtained $\lambda _\mathrm{eff}^{<2>}$ was four order of magnitude larger compared with ZnO bulk material (2.5 pm/V).     

Fabrication,morphologies and structural characterization of InN nanowire arrays

Large-scale, uniform diameter, and high-aligned metal indium was first introduced into the nanochannels of anodic aluminum membrane by electrochemical deposition. InN nanowires were achieved by the reaction of indium vapor with a constant flowing ammonia atmosphere. X-ray diffraction, scanning electron microscopy, and transmission electron microscopy were used to measure the size and structure of the sample. The results show that InN nanowires were aligned in the nanochannels of the template and the diameters were about 40 nm. Raman-scattering spectrum of InN nanowire array is presented. The \({ A}_{1}\) (TO), \({ E}_{1}\) (TO), and \({ E}_{2}\) (high) phonon frequencies at 440, 472, and 490 cm \(^{-1}\) were observed. The Raman spectrum of the InN nanowire arrays is consistent with the hexagonal wurtzite structure bulk InN, in agreement with X-ray diffraction observation.     

A DFG-based cavity ring-down spectrometer for trace gas sensing in the mid-infrared

Continuing studies into an all-diode laser-based 3.3 μm difference frequency generation cavity ring-down spectroscopy system are presented. Light from a 1,560 nm diode laser, amplified by an erbium-doped fibre amplifier, was mixed with 1,064 nm diode laser radiation in a bulk periodically poled lithium niobate crystal to generate 16 μW of mid-IR light at 3,346 nm with a conversion efficiency of $0.05\,\%\,{\text{W}}^{-1}\,{\text{cm}}^{-1}$ . This radiation was coupled into a 77 cm long linear cavity with average mirror reflectivities of 0.9996, and a measured baseline ring-down time of $6.07\pm 0.03\,\upmu{\rm s}$ . The potential of such a spectrometer was illustrated by investigating the $P(3)$ transition in the fundamental $\nu_{3}(F_{2})$ band of ${\text{CH}}_4$ both in a 7.5 ppmv calibrated mixture of ${\text{CH}}_4$ in air and in breath samples from methane and non-methane producers under conditions where the minimum detectable absorption coefficient ( $\alpha_{\rm min}$ ) was $2.8 \times 10^{-8}\,{\rm cm}^{-1}$ over 6 s using a ring-down time acquisition rate of 20 Hz. Allan variance measurements indicated an optimum $\alpha_{\rm min}$ of $2.9\times 10^{-9}\,{\rm cm}^{-1}$ over 44 s.     

Photodissociation of trapped \mathrm{H}_{2}^{+} ions for REMPD spectroscopy

We study the photodissociation of trapped $\mathrm{H}_{2}^{+}$ ions by 248?nm light from an excimer laser. Our results are in good agreement with calculated populations and photodissociation cross sections of the involved vibrational levels and yield a determination of the ion cloud radius. These data are used to obtain a reliable estimate of the efficiency of the resonance-enhanced multiphoton dissociation (REMPD) scheme in our $\mathrm{H}_{2}^{+}$ vibrational spectroscopy experiment. We go on to estimate the expected signal-to-noise ratio and discuss future improvements of the experimental setup.     

BN thin film as thermal interface mateiral for high power LED: thermal resistance and optical analysis

Over heat in junction temperature of an LED can impact the luminous performance of the lighting system. The more heat extracted from the system, the easier the LEDs can be driven; resulting in more light output and possibly a reduction in the number of LEDs needed to achieve the desired level of light output. Consequently, thin film based thermal interface mateiral (TIM) has been suggested and BN thin film was prepared on Cu substrate which is used as TIM. The 3W green LED was tested with BN thin film interface and observed low $T_{J}$ and total thermal resistance (R $_\mathrm{th-tot})$ value at 700 mA. The $\Delta T_{J}$ was 3.79  $^\circ $ C which was high compared to bare Cu. Overall, BN thin films was performed well on maintaining both the $T_{J}$ and the optical output considerably and could be an alternative for commersial thermal paste.     

Quasi solid state dye-sensitized solar cells based on polyvinyl alcohol (PVA) electrolytes containing \mathbf{I}^{\mathbf{-}}/\mathbf{I}_{\mathbf{3}}^{\mathbf{-}} redox couple

Quasi solid state dye-sensitized solar cells (DSSCs) have been fabricated with electrolytes containing $\text{ I }^{-}/\text{ I }_{3}^{-}$ redox couple using 80 % hydrolyzed polyvinyl alcohol (PVA) doped with potassium iodide (KI) and a mixture of potassium iodide and tetrapropyl ammonium iodide ( $\text{ Pr }_{4}\text{ NI }$ ) salts. The quasi solid state gel polymer electrolytes were prepared using 1:1 ethylene carbonate (EC):propylene carbonate (PC) mixture. The solar cells have the structure of ITO/ $\text{ TiO }_{2}$ /N3-Dye/electrolyte/Pt/ITO. The conductivity of the electrolytes has been calculated from the bulk resistance value determined using the electrochemical impedance spectroscopy. The performance of the DSSCs has been studied by varying the concentration of the doping salts in the electrolyte and incident light intensity. The DSSC fabricated with the KI salt electrolyte containing 9.9 wt% PVA, 39.6 wt% EC, 39.6 wt% PC, 10.9 wt% KI $(+\text{ I }_{2})$ exhibited the best power conversion efficiency of 1.97 %. However, the DSSC with a double-salt electrolyte containing 9.9 wt% PVA: 39.6 wt% EC: 39.6 wt% PC: (6.5 wt% KI: 4.4 wt% $\text{ Pr }_{4}\text{ NI }$ ) ( $+\text{ I }_{2}$ ) exhibited a higher efficiency of 3.27% under $100 \text{ mW/cm }^{2}$ light intensity. The efficiency of this cell increased to 4.59 % under dimmer light of intensity of $54 \text{ mW/cm }^{2}$ .     

Extremely large bandwidth and ultralow-dispersion slow light in photonic crystal waveguides with magnetically controllability

A line-defect waveguide within a two-dimensional magnetic-fluid-based photonic crystal with 45^o-rotated square lattice is presented to have excellent slow light properties. The bandwidth centered at $ \lambda_{0} $  = 1,550 nm of our designed W1 waveguide is around 66 nm, which is very large than that of the conventional W1 waveguide as well as the corresponding optimized structures based on photonic crystal with triangular lattice. The obtained group velocity dispersion $ \beta_{2} $ within the bandwidth is ultralow and varies from ?1,191 $ a/(2\pi c^{2} ) $ to 855 $ a/(2\pi c^{2} ) $ (a and c are the period of the lattice and the light speed in vacuum, respectively). Simultaneously, the normalized delay-bandwidth product is relatively large and almost invariant with magnetic field strength. It is indicated that using magnetic fluid as one of the constitutive materials of the photonic crystal structures can enable the magnetically fine tunability of the slow light in online mode. The concept and results of this work may give a guideline for studying and realizing tunable slow light based on the external-stimulus-responsive materials.     

Effects of cerium dopant concentration on structural properties and photocatalytic activity of electrospun Ce-doped TiO2 nanofibers

Electrospun \(\hbox {TiO}_2\) and Ce-doped \(\hbox {TiO}_2\) nanofibers were prepared with 0.5, 2.0 and 8.0 % weight Ce. The structural properties and phase composition were characterized using high-resolution transmission electron microscopy (HR-TEM), X-ray diffraction and X-ray absorption near edge spectroscopy (XANES) at the Ti K-edge. The undoped nanofibers are composed of an assembly of \(\hbox {TiO}_2\) nanoparticles and their crystal structure is a mixture of anatase and rutile phases with an anatase:rutile volume ratio close to 3:1. As Ce is introduced, the nanoparticles decrease in size and the rutile phase volume decreases. Ce \(\hbox {L}_3\) -edge XANES probed the local structure of Ce dopants. At 0.5 % Ce, most Ce ions are incorporated in the \(\hbox {Ce}^{3+}\) charge state but, at 2 % Ce, the majority are \(\hbox {Ce}^{4+}\) . Visible light absorption indicated that \(\hbox {Ce}^{3+}\) act as shallow acceptors that only participate in absorption of wavelengths below 420 nm but \(\hbox {Ce}^{4+}\) impurity states are associated with absorption of wavelengths up to 550 nm. Photocatalytic performance of the nanofibers was assessed by measuring the degradation of adsorbed Rhodamine B in aqueous solution under visible and ultraviolet light. The 0.5 % Ce-doped \(\hbox {TiO}_2\) nanofiber showed the best visible-light photocatalytic activity, which is probably due to the majority presence of \(\hbox {Ce}^{3+}\) . At higher Ce concentration, the photocatalytic reaction rate was lower than undoped nanofibers, indicating that recombination at the \(\hbox {Ce}^{4+}\) sites is rate limiting.     

Design of spectral crosstalk suppressing structure in two-color HgCdTe infrared focal plane arrays detector

Spectral crosstalk suppressing design of two-color HgCdTe medium-wave/long-wave (MW/LW) \(\hbox {n}^{+}\) – \(\hbox {p}_{1}\) – \(\hbox {P}_{2}\) – \(\hbox {P}_{3}\) – \(\hbox {N}^{+}\) infrared focal plane arrays (IRFPAs) detector functioning in simultaneous mode is carried out in this study, using Crosslight Technology Computer Aided Design (TCAD) software. A compositional barrier of \(\hbox {P}_{2}\) -region sandwiched between LW absorption layer of \(\hbox {p}_{1}\) -region and MW absorption layer of \(\hbox {P}_{3}\) -region is designed to suppress spectral crosstalk. MW-to-LW crosstalk can be significantly suppressed to 2.1 % while LW-to-MW crosstalk can be maintained less than 1 % by integrating an optimized compositional barrier.     

Ultra compact hybrid plasmonic–photonic coupler: configuration of metal–silica–silicon

In this work, a novel and practical configuration as a hybrid plasmonic–photonic coupler based on silicon (Si) nanofibers, silica waveguides and metal nanoparticles is examined and investigated. All of utilized waveguides, fibers and nanoparticles are embedded in an \(\hbox {Mg}_{2}\hbox {F}\) crystal host. Integrated plasmonic–photonic coupler provides significant transmission efficiency during guiding and propagating of light. Utilizing enhanced plasmonic waveguides helps to reduce the inherent losses such as scattering into the far-field and absorption of optical power inside the employed components, especially in nanoparticles. The transmission loss component under transverse electric excitation (TE) for the superstructure has been calculated as approximately \(\gamma _{T}=3\,\hbox {dB}/675\)  nm. Also, we investigate the coupling efficiency at overlapping regions between Si nanofibers and silica ( \(\hbox {SiO}_{2})\) waveguides which is referred to near-field interactions. Transmitted power ratio and the group velocity of the propagated light are computed and depicted for the proposed coupler.     

Preliminary studies of the Raman spectra of \hbox {Ag}_{2}\hbox {Te}\hbox { and }\hbox {Ag}_{5}\hbox {Te}_{3}

The theoretical calculations indicated that the monoclinic low-temperature phase of silver telluride $(\upbeta \hbox {-Ag}_{2}\hbox {Te})$ is a new binary topological insulator with highly anisotropic single Dirac cone surface. We obtained $\upbeta \hbox {-Ag}_{2}\hbox {Te}$ crystal ingots containing few grains by the Bridgman method. We also deposited thin films of tellurium, $\hbox {Ag}_{5}\hbox {Te}_{3}\hbox { and }(\hbox {Te+Ag}_{5}\hbox {Te}_{3})$ by thermal evaporation method. The Raman spectra of $\upbeta \hbox {-Ag}_{2}\hbox {Te}$ , tellurium and $\hbox {Ag}_{5}\hbox {Te}_{3}$ were measured at three excitation wave lengths: 633, 515 and 488 nm. The Raman active modes of $\upbeta \hbox {-Ag}_{2}\hbox {Te}$ , tellurium and $\hbox {Ag}_{5}\hbox {Te}_{3}$ are situated at frequencies below 300  $\hbox {cm}^{-1}$ while vibrations of other phases appear at higher frequencies.     

\mathrm{CO}_{2}^{*} chemiluminescence study at low and elevated pressures

Chemiluminescence experiments have been performed to assess the state of current $\mathrm{CO}_{2}^{*}$ kinetics modeling. The difficulty with modeling $\mathrm{CO}_{2}^{*}$ lies in its broad emission spectrum, making it a challenge to isolate it from background emission of species such as CH^? and CH₂O^?. Experiments were performed in a mixture of 0.0005H₂+0.01N₂O+0.03CO+0.9595Ar in an attempt to isolate $\mathrm{CO}_{2}^{*}$ emission. Temperatures ranged from 1654 K to 2221 K at two average pressures, 1.4 and 10.4 atm. The unique time histories of the various chemiluminescence species in the unconventional mixture employed at these conditions allow for easy identification of the $\mathrm{CO}_{2}^{*}$ concentration. Two different wavelengths to capture $\mathrm{CO}_{2}^{*}$ were used; one optical filter was centered at 415 nm and the other at 458 nm. The use of these two different wavelengths was done to verify that broadband $\mathrm{CO}_{2}^{*}$ was in fact being captured, and not emission from other species such as CH^? and CH₂O^?. As a baseline for time history and peak magnitude comparison, OH^? emission was captured at 307 nm simultaneously with the two $\mathrm{CO}_{2}^{*}$ filters. The results from the two $\mathrm{CO}_{2}^{*}$ filters were consistent with each other, implying that indeed the same species (i.e., $\mathrm{CO}_{2}^{*}$ ) was being measured at both wavelengths. A first-generation kinetics model for $\mathrm{CO}_{2}^{*}$ and CH₂O^? was developed, since no comprehensively validated one exists to date. CH₂O^? and CH^? were ruled out as being present in the experiments at any measurable level, based on calculations and comparisons with the data. Agreement with the $\mathrm{CO}_{2}^{*}$ model was only fair, which necessitates future improvements for a better understanding of $\mathrm{CO}_{2}^{*}$ chemiluminescence as well as the kinetics of the ground state species.     

One-step hydrothermal synthesis of nitrogen and tungsten codoped TiO2 nanorods with high visible light photocatalytic activity

N,W codoped TiO 2 $\mathrm{TiO}_{2}$ nanorods were synthesized via a one-step hydrothermal method using ammonium metatungstate as the nitrogen and tungstate sources. The prepared samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), UV–visible diffuse reflectance spectroscopy (DRS), and X-ray photoelectron spectroscopy (XPS). The results indicated that the N,W codoped TiO 2 $\mathrm{TiO}_{2}$ nanorods exhibited a higher photocatalytic activity under visible light irradiation compared with P25 and undoped TiO 2 $\mathrm{TiO}_{2}$ , because the codoping of N and W ions not only extended the visible light absorption but also promoted the separation of the photogenerated electrons and holes.     

Characterization of a large core photonic crystal fiber made of lead–bismuth–gallium oxide glass for broadband infrared transmission

We report on characterization of a large solid core, photonic crystal fiber dedicated to broadband transmission range from visible to mid-infrared. We have fabricated a multi-mode photonic crystal fiber, made of a heavy metal-oxide glass based on the $\hbox {PbO}{-}\hbox {Bi}_{2}\hbox {O}_{3}{-}\hbox {Ga}_{2}\hbox {O}_{3}$ system, modified with $\hbox {SiO}_{2}$ and CdO, synthesized in-house, which shows good transmission up to $4.5\,\upmu \hbox {m}$ , as well as good rheological properties that permit multiple thermal processing steps without crystallization. The core of the fiber is created by replacement of central 60 tubes with solid rods. The photonic cladding is composed of 8 rings of air holes with a filling factor of 0.42. Simulation results shows that the fiber can be used for broadband transmission in the range of 430–3,000 nm. Calculated effective mode area of the fiber is $295\,\upmu \hbox {m}^{2}$ . We have measured attenuation of the fiber in the range 800–1,700 nm and its sensitivity to bending losses. Attenuation ranges from 1 to 4 dB/m in the considered range and bending losses are below 0.7 dB.     

Femtosecond relaxation kinetics of highly excited \mathrm{M}_{\mathrm{Na}}^{**} states in CaF2 at 3.2 eV and 4.7 eV

Femtosecond (fs) laser pulses at variable delay times allowed us to track the fast non-radiative transitions between the manifold of highly excited $\mathrm{M}_{\mathrm{Na}}^{**}$ states to the lower lying fluorescent $\mathrm{M}_{\mathrm{Na}}^{*}$ state in CaF₂. Two distinct $\mathrm{M}_{\mathrm{Na}}^{**}$ states of the manifold at 3.16?eV ( $\mathrm{M}_{\mathrm{Na}2}^{**}$ ) and 4.73?eV ( $\mathrm{M}_{\mathrm{Na}3}^{**}$ ) were populated using the second (SH) and third harmonics (TH) of fs laser light at 785?nm. The population kinetics of the fluorescent $\mathrm{M}_{\mathrm{Na}}^{*}$ state in the 2?eV excitation energy range was revealed by depleting its fluorescence centered at 740?nm using fundamental near infrared (NIR) fs laser pulses. The related time constants for $\mathrm{M}_{\mathrm{Na}2,3}^{**}{\sim}{>} \mathrm{M}_{\mathrm{Na}}^{*}$ relaxation amounted to 1.0±0.14?ps and 3.0±0.3?ps upon SH and TH excitation, respectively.     

All-carbon detector with buried graphite pillars in CVD diamond

A diamond detector of 3D architecture without any metallization is developed for spectroscopy of ionizing radiation and single particles detection. The carbon electrode system was fabricated using a femtosecond infrared laser ( $\lambda $ = 1,030 nm) to induce graphitization on the surface and inside 4.0  $\times $  4.0  $\times $  0.4 mm $^{3}$ single-crystal chemical vapor deposition diamond slab, resulting in an array of 84 buried graphite pillars of 30  $\upmu $ m diameter formed orthogonally to the surface and connected by surface graphite strips. Sensitivity to ionizing radiation with $^{90}$ Sr $\upbeta $ -source has been measured for the 3D detector and high charge collection efficiency is demonstrated.     

Simulation and optimization of reflection optical module design for single LED

Illuminance uniformity and illuminating efficiency are always the key problems of light emitting diode (LED) lighting system design. Based on the new design of the reflection optical module, illuminance uniformity and illuminating efficiency are investigated simultaneously in this paper. At the first stage, a reflector with various profile designs is installed to improve the uniformity and efficiency of irradiances collected through the receiver. Using the macro commands, an effective process is presented through the optimal design of the reflector geometries, and the merit function is used as the optical quality objective to find the optimal design value of $K2$ K 2 and $R2$ R 2 parameters of the reflector. At the second stage, based on the optimal design result, the displacement between LED source and reflector is further adjusted automatically by the macro commands too. The results from the ray tracing simulation indicate that the optimal design can be achieved through the compromise of Illuminance uniformity and illuminating efficiency. Finally, we obtain the merit function value of $1.81$ 1.81 with $K2=-1.09, R2=1.11\,\hbox {mm}$ K 2 = - 1.09 , R 2 = 1.11 mm , and the source position $Z1= 1.68\,\hbox {mm}$ Z 1 = 1.68 mm . The results shown in this paper could be beneficial for machine vision systems which are heavily demanded in the light source applications for the uniform and efficient illuminance.     

Dye-sensitized solar cells with PVA–KI–EC–PC gel electrolytes

Gel polymer electrolytes consisting of PVA–EC–PC–KI have been studied in this work. The highest room temperature (298 K) conductivity of 12.92 mS cm $^{-1}$ is obtained for PVA-based gel polymer electrolyte (GPE) with composition 14.5 PVA-21.7 EC-28.7 PC-30.4 KI-4.7 $\text{ I }_{2}$ (in wt%). The high conductivity is due to the highest number density of mobile ions in the electrolyte. The conductivity–temperature dependence follows the Vogel–Tamman–Fulcher (VTF) relationship. The trend of pseudoactivation energy $(E_{a})$ with salt concentration is contrary to that of conductivity. PVA-based GPEs with 5 to 35 wt% KI were used as a medium in ruthenium 535 (N719) dye-sensitized solar cells. The efficiency ( $\eta $ ) of the solar cells increased as the composition of KI salt in the electrolyte increased. The highest power conversion efficiency of 2.74 % is obtained for solar cells fabricated with electrolyte containing 35 wt% KI. The variation of efficiency follows the same trend as short circuit current density $(J_{sc})$ . The increase in $J_{sc}$ is influenced by the increase in iodide ion concentration in the electrolyte that assists the redox process and helps electron to shuttle between ionized dye and counter electrode.