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At least 829 records · Page 46

Photoluminescence investigations on Sm3+ ions doped borate glasses for tricolor w-LEDs and lasers

Highlights: • Borate glasses with Sm3+ ions were synthesized by melt quenching technique. • Under 402 nm excitation Borate glasses show reddish orange luminescence. • Energy transfer through cross-relaxation leads to fall in decay time of Sm3+ ions. • I-H model confirms energy transfer between Sm3+ ions as dipole-dipole in nature. • 1 mol% Sm3+ ions in these glasses are apt for red photonic device applications. - Abstract: This work describes mainly the optical absorption, photoluminescence (PL) and decay spectral properties of Sm{sup 3+} ions doped borate glasses to understand their possible usage in tricolor w-LEDs and lasers.The XRD spectrum recorded for an un-doped glass confirms glassy nature of the as prepared glass. The Judd-Ofelt (J-O) intensity parameters evaluated from experimental oscillator strengths were used in estimating the various radiative parameters. Under 402 nm excitation, the PL spectra exhibit intense emission at 600 nm for which the decay spectral profiles were recorded.The decay profiles are converting from single exponential to non-exponential with increase in Sm{sup 3+} ion concentration ensuing decrease in experimental lifetimes which may be attributed to the efficient energy transfer through cross-relaxation process. The non-exponential decay curves fitted to I-H model reveals the interaction between the Sm{sup 3+} ions as dipole-dipole in nature. From the evaluated emission cross-sections, quantum efficiency, branching ratios and CIE co-ordinates, it is concluded that 1 mol% Sm{sup 3+} ions in these glasses are aptly suitable to fabricate reddish-orange luminescent devices.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Synthesis of cuboid BiOCl nanosheets coupled with CdS quantum dots by region-selective deposition process with enhanced photocatalytic activity

Highlights: • Region-selective deposition process was adopted to prepare high-dispersed CdS QDs/BiOCl nanocomposites consisting of cuboid BiOCl nanosheets exposing (001) facet and CdS QDs with size of 5–10 nm. • The TGA was used as bridge linked the CdS QDs and BiOCl, which enables CdS QDs spread homogeneously on the (001) facet of BiOCl. • The optical absorption properties and charge transfer efficiency of CdS QDs/BiOCl nanocomposites are much improved owing to the widespread heterojunction between CdS QDs and BiOCl. • The photocatalytic degradation activities of CdS QDs/BiOCl composites are excellent for MO dyes and phenol contaminants under simulated solar and UV light, respectively. - Abstract: A facile region-selective deposition process was adopted to prepare high-dispersed CdS QDs on BiOCl nanosheets with the surface modification of thioglycollic acid (TGA). The samples were systematically characterized by XRD, SEM, TEM, HRTEM, EDS, XPS, UV–vis DRS, EIS and PL. The results indicate that CdS QDs with size of 5–10 nm dispersed uniformly on the surface of cuboid BiOCl nanosheets. The photocatalytic performance tests reveal that the CdS QDs-3%/BiOCl composite exhibits an excellent photocatalytic activity, which is over 4.0 and 4.8 times as high as pure BiOCl for methyl orange (MO) and phenol photodegradation rate under simulated solar light and UV light illumination, respectively. The enhanced photocatalytic performance of the CdS QDs/BiOCl composites should be attributed to the improved visible light absorption and the high migration efficiency of the photogenerated electron-holes due to the matched band gap and the widespread heterostructure between CdS QDs and BiOCl.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Improving on the interparticle connection for performance enhancement of flexible quantum dot sensitized solar cells

Highlights: • TiO{sub 2} slurries have been prepared by a three-step process for the photo-anode of flexible solar cells. • Interparticle connection of photo-anodes has been improved in flexible solar cells. • This flexible QDSSCs exhibits excellent photovoltaic performance and charge transfer property. • There has excellent curving stability on the photovoltaic performance of flexible QDSSCs. - Abstract: Flexible photovoltaic devices have wide applications in many unique areas. However, the interparticle connection of photo-electrode in flexible photovoltaic devices still needs to be improved. Here, TiO{sub 2} slurries have been prepared by a three-step process, which are employed to prepare the photo-anode for flexible CuInS{sub 2} quantum dot sensitized solar cells (QDSSCs). 5 nm-sized TiO{sub 2} nanoparticles and hydrochloric acid (HCl) have been introduced in 20 nm-sized TiO{sub 2} based photo-electrodes under TiO{sub 2}/HCl mass ratio of 3:1, which exhibits excellent photovoltaic performance and charge transfer property. Due to the interparticle connection enhancement by suitable content of 5 nm-sized TiO{sub 2} nanoparticles, photo-anodes with the 20/5-TiO{sub 2} nanoparticles mass ratio of 3:1 exhibits the better optical absorption property and photovoltaic performance of flexible QDSSCs. Moreover, there has maintained 98% photovoltaic conversion efficiency of flexible QDSSCs with the seriously curving condition, which can be considered the great foreground in future applications.

14 SOLAR ENERGY↗

Multiwalled carbon nanotubes in titania based nanocomposite as trap for photoexcitons for enhanced photocatalytic hydrogen production under solar light irradiation

Highlights: • Facile synthesis of FCNTs-TiO{sub 2} composite through wet impregnation method. • Parameters were optimized for enhanced photocatalytic hydrogen production under sunlight irradiation. • At optimal conditions nanocomposite showed 8 folds higher hydrogen efficiency than pristine TiO{sub 2}. • Functionalized carbon nanotubes acts as cocatalyst in this study. - Abstract: The impact of functionalized multiwalled carbon nanotubes in titania based nanocomposite for photocatalytic hydrogen production was investigated. Founctionalization experiments were carried out to remove amorphous carbon atttached to carbon nanotubes by strong acid treatment followed by calcination at desired temperature and time intervals. Materials characterization revealed that anatase TiO{sub 2} nanoparticles randomly dispersed onto the walls of one dimensional multiwalled carbon nanotubes with surface hydroxyl and carbonyl groups besides significant change in optical absorption. Photocatalytic activity was performed in aqueous glycerol solution under solar light and volume of hydrogen production was quantified using gas chromatography. Highest hydrogen production rate of 13,107 μmol·h{sup −1}·g{sup −1} of catalyst was recorded under optimized conditions due to cocatalyst role of functionalized carbon nanotubes. Here, photo electrons were trapped by carbon nanotubes for continuous hydrogen production through reduction reaction.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Surface-polarity-dependent ferromagnetism in arsenic-implanted ZnO films prepared by MBE

O-polar and Zn-polar ZnO films were prepared by rf-plasma assisted molecular beam epitaxy (MBE) on sapphire substrates. Arsenic ions have been implanted into high quality ZnO with a definite polarity. Substantial temperature-independent ferromagnetism has been observed for both films, with the O-polar film having approximately twice the magnetization as the Zn-polar film. The saturation magnetization is shown to be due to the defects introduced during implantation, rather than to local moments associated with the As ion. Rutherford Backscattering/Channeling and optical absorption measurements confirm that the implantation introduces more defect states in the O-polar films, while X-ray absorption near-edge structure measurements show that the environment of the arsenic ions was similar for both polarities. (C) 2014 Elsevier B.V. All rights reserved.

Doped ZnO↗

Lithium indium diselenide — An advanced material for neutron detection

Here, this paper describes the synthesis, crystal growth, detector fabrication, radiation hardening studies, MCNP modeling, and characterization of lithium indium diselenide or LiInSe 2 . This newly-developed room temperature thermal neutron detector has semiconducting and scintillating properties and it is suitable for neutron detection application. LiInSe 2 was synthesized starting from elemental Li, In, Se in two steps due to high reactivity of Li. A single crystal of LiInSe 2 was grown using the Vertical Bridgman method. The room temperature band gap was found to be 2.8 eV using optical absorption measurements. Bulk resistivity was measured at ∼5 × 10 11 Ωcm. Photoconductivity measurements of LiInSe 2 wafers identified a peak in the photocurrent around 445 nm. Nuclear radiation detectors were fabricated from single crystal wafer and the responses to alpha particles at various biases were measured. The mobility-lifetime product was estimated. Gamma irradiation studies were performed with calculated absorbed doses ranging from 0.2126 to 21,262 Gy. The characterization of the two wafers for their scintillator performance was conducted after each irradiation. The gamma irradiation produced a reduction of the light yield that translated to a lower channel number for the centroid of alpha detection spectra. It also showed a considerable reduction of the decay time after the first irradiation. These are the first studies on gamma radiation hardening with this material.

46 INSTRUMENTATION RELATED TO NUCLEAR SCIENCE AND ↗

A method to load tellurium in liquid scintillator for the study of neutrinoless double beta decay

Herein, a method has been developed to load tellurium into liquid scintillator so as to permit searches for neutrinoless double beta decay with high sensitivity. The approach involves the synthesis of an oil-soluble tellurium compound from telluric acid and an organic diol. The process utilises distillable chemicals that can be safely handled underground and affords low radioactive backgrounds, low optical absorption and high light yields at loading levels of at least several percent Te by weight.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗

Luminescence and scintillation properties of XPO 4 :Nd 3+ (X = Y, Lu, Sc, La) crystals

Due to their very fast short-wavelength emission, neodymium-doped materials are a subject of current interest as potential scintillators. Although the initial reports regarding neodymium-doped orthophosphates (in crystalline form) and their scintillation properties appeared almost twenty years ago, they remain an interesting class of materials since there is no in-depth understanding of their fundamental scintillation mechanism. In the present research, we focus on the crystalline systems: XPO 4 :Nd 3+ , where X = Y, Lu, La, Sc. The pulse height, optical absorption, radioluminescence and photoluminescence spectra were investigated and are reported here for various temperatures from 10 to 350 K. Here, results of both low and high temperature thermoluminescence measurements are reported in this communication.

36 MATERIALS SCIENCE↗

What is really extraordinary in cuprate superconductors?

Over the course of three decades of intense study, apart from the exceptionally high critical temperature, many unusual properties of cuprates have been discovered, notably including resistivity linear in temperature, electronic Raman continuum and optical absorption extending throughout the infrared region, pseudogap, hour-glass spin excitation spectrum, etc. However, each of these features have been also observed in other materials, including some that are not even superconducting at all. Here, we describe an extensive experiment in which over 2,000 films of the La 2-x Sr x CuO 4 have been synthesized and studied in detail over the course of the last twelve years. We argue here that, uniquely, in the cuprates an unusual superconducting state, that defies the standard BCS description, develops from an unusual metallic state, in which the rotational symmetry of the electron fluid is spontaneously broken.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Photo-oxidation of polymer-like amorphous hydrogenated carbon under visible light illumination

Amorphous hydrogenated carbon (a-C:H), a polymer-like network typically synthesized by plasma chemical vapor deposition, has long been understood to exhibit optical absorption of visible light (λ > 400 nm). In this report we explain that this absorption is accompanied by rapid photo-oxidation (within minutes) that behaves in most respects like classic polymer photo-oxidation with the exception that it occurs under visible light illumination rather than ultraviolet illumination.

36 MATERIALS SCIENCE↗

Surface oxygen exchange kinetics of mixed conducting oxides: Dilatometric vs electrical conductivity relaxation study

The surface oxygen exchange kinetics of mixed ionic-electronic conducting (MIEC) oxides play a crucial role in a variety of applications, including solid oxide fuel/electrolysis cells (SOFCs/SOECs), permeation membranes and sensors. To date, a variety of methods, including isotope exchange, electrical conductivity, optical absorptivity and thermogravimetry relaxation, and impedance spectroscopy have been used to measure the oxygen exchange coefficient of MIEC oxides. Each of these methods have their advantages and limitations, depending on the physical and chemical properties of the investigated materials and their sample dimensions and densities. Here, we demonstrate the ability to precisely measure the surface oxygen exchange coefficient (k chem ) of MIEC model material Pr 0.1 Ce 0.9 O 2-δ (PCO) by use of dilatometric relaxation measurements, particularly of interest for materials that exhibit larger chemical expansion coefficients. This is achieved by use of porous bulk specimens to ensure that the contribution of oxygen exchange to the overall kinetics is dominant. We demonstrate that k chem values extracted from chemical expansion relaxation measurements on PCO are nearly identical to those derived from electrical conductivity relaxation measurements. As a result, this provides the opportunity to precisely investigate the oxygen exchange and chemical expansion kinetics of a wide range of materials used in high-temperature applications, particularly where more conventional methods are difficult or inappropriate to apply.

(Pr,Ce)O2-x↗

Revealing optoelectronic and transport properties of potential perovskites Cs 2 PdX 6 (X = Cl, Br): A probe from density functional theory (DFT)

Metal-halide perovskites are rapidly emerging crystalline materials that are reasonably preferred as leading aspirant for applications in optoelectronic and thermoelectric devices. In this paper, we have thoroughly reviewed and performed calculations to reveal optoelectronic and transport properties for a potential newcomer, Cs 2 PdX 6 (X = Cl, Br) termed as Cesium Palladium Halides (CPH). Outcome of present computations are compared with available results and a reasonable agreement is recorded. Energy band gap computations performed reveal indirect band gap of 2.29 eV for Cs 2 PdCl 6 , which substantially reduces to 1.22 eV when ‘Cl’ is replaced by ‘Br’. Optical absorption spectra investigations performed here, in the energy range from 3 to 5 eV confirms effective utilization of these compounds in solar cells and other optoelectronic applications. In addition, the transport properties computations performed using semi-classical Boltzmann theory, shows constant pattern of thermo power near ambient temperature range (200–500 K), which admits possible utilization of these compounds as low temperature thermoelectric materials. Performed ZT calculations demonstrates reasonably good thermoelectric performance for both materials, as there exist minor variation (0.1) in the values over wide temperature ranges i.e. from 100 to 800 K. Further, detailed analysis of transport properties predicts p-type semiconducting nature of the present series of materials.

Bhamu, K. C.↗

Self-regulated growth and tunable properties of CuSbS 2 solar absorbers

Polycrystalline thin film copper chalcogenide solar cells show remarkable efficiencies, and analogous but less-explored semiconducting materials may hold similar promise. With consideration of elemental abundance and process scalability, we explore the potential of the Cu–Sb–S material system for photovoltaic applications. Using a high-throughput combinatorial approach, Cu–Sb–S libraries were synthesized by magnetron co-sputtering of Cu 2 S and Sb 2 S 3 targets and evaluated by a suite of spatially resolved characterization techniques. The resulting compounds include Cu 1.8 S (digenite), Cu 12 Sb 4 S 13 (tetrahedrite), CuSbS 2 (chalcostibite), and Sb 2 S 3 (stibnite). Of the two ternary phases synthesized, CuSbS 2 was found to have the most potential, however, when deposited at low temperatures its electrical conductivity varied by several orders of magnitude due to the presence of impurities. To address this issue, we developed a self-regulated approach to synthesize stoichiometric CuSbS 2 films using excess Sb 2 S 3 vapor at elevated substrate temperatures. Theoretical calculations explain that phase-pure CuSbS2 is expected to be formed over a relatively wide range of temperatures and pressures, bound by the sublimation of Sb2S3 and decomposition of CuSbS2. The carrier concentration of CuSbS 2 films produced within this regime was tunable from 10 16 – 10 18 cm –3 through appropriate control of Sb 2 S 3 flux rate and substrate temperature. CuSbS 2 displayed a sharp optical absorption onset indicative of a direct transition at 1.5 eV and an absorption coefficient of 10 5 cm −1 within 0.3 eV of the onset. Furthermore, the results of this study suggest that CuSbS 2 holds promise for solar energy conversion due to its tolerant processing window, tunable carrier concentration, solar-matched band gap, and high absorption coefficient.

14 SOLAR ENERGY↗

Reactive ion etched, self-aligned, selective area poly-Si/SiO 2 passivated contacts

Front/back poly-Si/SiO 2 contact devices suffer from low short-circuit current density, J sc , due to parasitic optical absorption in the front poly-Si layer. Thin poly-Si (~20 nm) allows for high J sc but is not compatible with screen-printed fire-through contacts. We therefore study the effects of post-deposition etching of a thick poly-Si (200 nm) front layer by reactive ion etching (RIE) using the metal grid lines as a self-aligned mask. We show that passivation is maintained in the device during RIE and that J sc is increased by a gain in the blue quantum efficiency response. However, our specific etching parameters cause non-uniform etching of the poly-Si leading to premature loss of passivation without optimal gain in J sc . Etched, unpassivated layers can be re-passivated with a H-containing dielectric layer leading to a gain in Jsc, open circuit voltage, V oc , Fill-Factor, FF, and efficiency.

14 SOLAR ENERGY↗

Damping of the Franz–Keldysh oscillations in the presence of disorder

Franz–Keldysh oscillations of the optical absorption in the presence of short-range disorder are studied theoretically. The magnitude of the effect depends on the relation between the mean-free path in a zero field and the distance between the turning points in electric field. As is adopted in the literature, turning points are the points where the net energy is equal to potential energy. Damping of the Franz–Keldysh oscillations by the disorder develops at high absorption frequency. Effect of damping is amplified by the fact that, that electron and hole are most sensitive to the disorder near the turning points. This is because, near the turning points, velocities of electron and hole turn to zero.

71 CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSIC↗

Two-Dimensional Copper Iodide-Based Inorganic–Organic Hybrid Semiconductors: Synthesis, Structures, and Optical and Transport Properties

A group of copper iodide-based hybrid semiconductors with the general formula of 2D-CuI(L) 0.5 (L = organic ligands) are synthesized and structurally characterized. All compounds are two-dimensional (2D) networks made of one-dimensional (1D) copper iodide staircase chains that are interconnected by bidentate nitrogen-containing ligands. Results from optical absorption and emission experiments and density functional theory (DFT) calculations reveal that their photoluminescence (PL) can be systematically tuned by adjusting the lowest unoccupied molecular orbital (LUMO) energies of the organic ligands. Charge carrier transport measurements were carried out for the first time on single crystals of selected 2D-CuI(L) 0.5 structures, and the results show that they possess p-type conductivity with a Hall mobility of ~1 cm 2 V -1 s -1 for 2D-CuI(pm) 0.5 and 0.13 cm 2 V -1 s -1 for 2D-CuI(pz) 0.5 , respectively. These values are comparable to or higher than the mobilities of typical highly luminescent organic semiconductors. Finally, this work suggests that robust, high-dimensional copper iodide hybrid semiconductors are promising candidates to be considered as a new type of emissive layer for light-emitting diode (LED) devices.

36 MATERIALS SCIENCE↗

Hybrid and Inorganic Vacancy-Ordered Double Perovskites A 2 WCl 6

We report hybrid and all-inorganic, vacancy-ordered double perovskites of d 2 W 4+ with the formula A 2 WCl 6 (A = CH 3 NH 3 + , Rb + , and Cs + ). These compounds, which are reddish in color, can be distinguished from structurally similar compounds obtained by hydrothermal methods on the basis of structure, spectroscopic, and magnetic properties. The latter are green and incorporate oxygen, with the actual formula Cs 2 WO x Cl 6–x and distinct optical absorption and emission behavior. Furthermore, the local-moment magnetism of the pure-red d 2 compounds reported here does not correspond to the appropriate Kotani model, suggesting as-yet undiscovered physics in these systems.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Layered and Low-Dimensional Lead, Silver, and Bismuth Halide Perovskites Directed by Halogen-Substituted Spacer Cations

Hybrid organic–inorganic metal halides provide a diverse parameter space in which the optoelectronic properties can be tuned through the composition. The compositional tunability extends to the metal site, which can be expanded from single valent metals (e.g., Pb 2+ ) to multivalent metals (e.g., Ag + and Bi 3+ ), and the dimension (2D, 1D, or 0D). However, a deeper understanding of how the organic cations template these metal halide structures is needed. Here, we synthesize and study the structures of a series of new layered and low-dimensional metal (Pb, Ag, and Bi) halides templated by the halogenated aryl spacer cations 2-chlorobenzylammonium (2ClBZ) and 3-chloro-2-fluorobenzylammonium (3Cl2FBZ). We report new lead perovskites, (3Cl2FBZ) 2 PbBr 4 , (2ClBZ) 3 PbI 5 , and (3Cl2FBZ) 2 PbI 4 , and compare them to their silver and/or bismuth analogs (2ClBZ) 4 AgBiBr 8 , (3Cl2FBZ) 4 AgBiBr 8 , (2ClBZ) 3 Bi 2 I 9 , and (3Cl2FBZ) 4 Bi 2 I 10 . In all structures, the halogen-substituted cations result in 2D or “pseudo-2D” layering, but the different halogen substituents introduce different distortions (tilting, octahedral distortion) and dimensional reduction to 1D or 0D depending on the metal and halide compositions. Optical absorption measurements reveal the bandgaps are tunable through metal sites, dimension, and cations to different extents. Furthermore, the 1D (3Cl2FBZ) 4 Bi 2 I 10 crystallizes in the noncentrosymmetric space group Cmc2 1 and exhibits second-harmonic generation (SHG). Furthermore, the organic–inorganic interactions and resultant structural distortions examined here provide insights toward the engineering of noncentrosymmetry and dimensional control in hybrid metal halide perovskites.

Cations↗