High-resolution Photoluminescence Research Articles

Down and Upconversion NGQDs and CuInS/ZnS QDs Nanocomposite for Ascorbic Acid Sensing

Copper indium sulfide/zinc sulfide (CuInS/ZnS) QDs and Nitrogen graphene quantum dots (NGQDs) were synthesized via aqueous solution methods and facile hydrothermal, respectively. Herein, according to the photoluminescence (PL) properties of QDs, a fluorescent nanocomposite of CuInS/ZnS QDs and NGQDs was synthesized. This nanocomposite was characterized by high-resolution transmission electron microscopy (HRTEM) and PL spectroscopy. This fluorescent nanocomposite was developed as a highly sensitive and selective ascorbic acid optical biosensor based on the luminescent quenching in the range from 10 to 500 μM with a correlation coefficient (R2) of 0.9964 and limit of detection (LOD) of 16.8 µM. HRTEM micrographs confirmed the preparation of CuInS/ZnS QDs with an average diameter size of 3 nm and NGQDs with an average diameter size of 5 nm.

High-Performance Sol-Gel-Derived CNT-ZnO Nanocomposite-Based Photodetectors with Controlled Surface Wrinkles.

We investigate the effects of incorporating single-walled carbon nanotubes (CNTs) into sol-gel-derived ZnO thin films to enhance their optoelectronic properties for photodetector applications. ZnO thin films were fabricated on c-plane sapphire substrates with varying CNT concentrations ranging from 0 to 2.0 wt%. Characterization techniques, including high-resolution X-ray diffraction, photoluminescence, and atomic force microscopy, demonstrated the preferential growth of the ZnO (002) facet and improved optical properties with the increase in the CNT content. Electrical measurements revealed that the optimal CNT concentration of 1.5 wt% resulted in a significant increase in the dark current (from 0.34 mA to 1.7 mA) and peak photocurrent (502.9 µA), along with enhanced photoresponsivity. The rising and falling times of the photocurrent were notably reduced at this concentration, indicating improved charge dynamics due to the formation of a p-CNT/n-ZnO heterojunction. The findings suggest that the incorporation of CNTs not only modifies the structural and optical characteristics of ZnO thin films but also significantly enhances their electrical performance, positioning CNT-ZnO composites as promising candidates for advanced photodetector technologies in optoelectronic applications.

Development of hydrophilic carbon fiber textiles using seed-assisted hydrothermal deposition of ZnO nanostructures for enhanced interfacial interaction in CFRP composites

Two-step hydrothermal deposition of zinc-oxide (ZnO) nanorods was used to functionalize carbon fiber textiles in order to produce increased hydrophilicity on fiber surface. On carbon fiber textiles, tightly packed ZnO nanorods developed after five seed cycles and 5 h of growth treatment in a 30 mM precursor salt based on the hydrothermal synthesis. Extensive characterizations have been performed on field emission scanning electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, Energy-dispersive X-ray spectroscopy, High resolution transmission electron microscopy, Photoluminescence spectroscopy, and Raman spectroscopy to assess the different aspects such as structural, morphological, elemental, and wettability of the plain and ZnO-modified carbon fiber textiles. ZnO nanomaterial having hexagonal nanorods shape and wurtzite crystalline structure were uniformly deposited on the fabrics. Owing to the wettability study, ZnO prisms improved the hydrophilicity of virgin carbon fiber textiles to enable strong bonds with polymer matrix. The findings highlight the significant improvement in the static water contact angle as a result of the samples' ZnO coating's ability to reduce surface free energy. The improved hydrophilicity in carbon fiber may enhance the bonding between carbon fibers and matrix materials in composite materials. Hydrophilic carbon fibers are more easily wetted by the matrix materials, allowing for better penetration of the matrix into the fiber structure.

Effective removal of textile dye via synergy of adsorption and photocatalysis over ZnS nanoparticles: Synthesis, modeling, and mechanism

In this work, we prepared sulfur-zinc nanoparticles (ZnS-TGA) functionalized with thioglycolic acid by a hydrothermal method and tested their photodegradation ability by solar irradiation. ZnS-TGA were characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), high-resolution transmission electron microscope (HR-TEM), UV–Vis spectrophotometer and photoluminescence spectroscopy. In the characterization of these nanoparticles, thioglycolic acid proved to be a strong capping ligand, with a specific surface area of 36.82 m2/g and an average size of 7.15 nm. To test the photocatalytic degradability of the product, methylene blue (MB) was used as a model pollutant. Various operational variables were investigated, including pH, amount of nanoparticles, dye concentration, contact time and temperature. The equilibrium adsorption tests, and the statistical physical calculations allowed the analysis of the energetic and steric variables of the adsorption of MB dye molecules on the surface of these nanoparticles. The equilibrium data were well fitted with Langmuir-Freundlich (L-F) and the adsorption kinetics with pseudo-first order. The maximum adsorption capacity of the MB dye removal process was 30.92 mg g−1 at pH 7 and 298 K, and this process was spontaneous and exothermic. The dye molecules and the surface of the nanoparticles exhibited physical interactions with adsorption energies of 23.31–25.92 kJ/mol. The photocatalytic activity of these nanoparticles resulted in a dye degradation efficiency of 91.1 % in 180 min. The photocatalytic efficiency remained almost unchanged after five consecutive degradation cycles, resulting in a methylene blue degradation of 85 %. According to these results, these environmentally friendly nanoparticles have the potential to purify industrial and urban liquids contaminated with harmful organic compounds such as dye molecules.

Porphyrin-based carbon dots as fluorescence probe for sensing of Fe3+ ion and S2- anion in aqueous solution

In this work, a facile bottom-up approach was employed to synthesize the porphyrin-citric acid-derived fluorescent carbon dots (Por-CA-CDs) using a single-step hydrothermal method. As-prepared Por-CA-CDs were well characterized using spectroscopic techniques such as FT-IR, high-resolution transmission electron microscopy, P-XRD, UV-Vis absorption, and photoluminescence spectroscopy. The synthesized Por-CA-CDs exhibited blue fluorescence with excellent photostability and diameter ranging from 2.4 to 6.4 nm. Por-CA-CDs show excitation-dependent emission behavior, with a quantum yield of 26% and were used for sensing of Fe3+ and S2− ions in an aqueous solution. Por-CA-CDs demonstrated a robust and selective reaction to Fe3+ compared to the other cations utilized in this investigation. The sensing capability of Por-CA-CDs with Fe3+ ions was evaluated with fluorescence spectroscopy, and results show a “Turn-Off” emission mode upon binding of Fe3+ with Por-CA-CDs. In metal ion sensing studies, the fluorescence intensity of Por-CA-CDs exhibited significant quenching upon the addition of Fe3+ at concentrations ranging from 0 to 230 μM, with a detection limit (LOD) of 3.2 × 10−8 M. The quenching efficiency and Stern-Volmer quenching constant were computed as 99.45% and 4.4 × 106 M−1, respectively. Interestingly, fluorescence of Por-CA-CDs can be regained with the addition of S2− (0-160 µM) with LOD of 4.3 × 10−6 M and Stern-Volmer quenching constant of 6 × 105 M−1. Most importantly, the toxicity assay revealed good reliability for samples in deionized, tap, and river water, suggesting applications for Fe3+ monitoring in complex environments.

A stable and regenerative TiO2/Bi2MoO6 photocatalyst for highly effective degradation of Rhodamine B and Congo Red

ABSTRACT This research unravels a facile method for synthesising TiO2/Bi2MoO6 photocatalysts and their effective applications in degrading industrial dyes. Initially, Bi2MoO6 was prepared as the substrate, followed by the addition of TiO2 to form the TiO2/Bi2MoO6 composite. The photocatalyst was characterised by powder X-ray diffraction (XRD), scanning electron microscopy with energy-dispersive X-ray spectrometry (SEM-EDS), X-ray photoelectron spectroscopy (XPS), high-resolution transmission electron microscopy (HR-TEM), photoluminescence (PL), and UV-Vis diffuse reflectance spectroscopy (UV-Vis DRS). Its photocatalytic properties were evaluated by dye degradation under various conditions, including different dopant loading amounts, the reaction time, the initial concentration of the dye, and pH values. The results indicated that 50 mg of 15% TiO2/Bi2MoO6 achieved the highest photodegradation efficiency: 98.51% for 50 mL 10 mg L−1 Rhodamine B (RhB) within 100 min in a neutral buffer solution and 90.71% for 50 mL 10 mg L−1 Congo Red (CR) within 80 min in an aqueous solution. This material exerted effectiveness across a wide pH range, with removal rates of RhB exceeding 95.41% in both acidic and alkaline conditions. The degradation process conformed to the pseudo-first-order kinetic model. Radical trapping experiments revealed that the dye degradation mechanism involved ∙ O 2 − and h+. Notably, the synthesised TiO2/Bi2MoO6 photocatalyst demonstrated high stability and reusability, maintaining performance even after four degradation cycles. The TiO2/Bi2MoO6 photocatalyst, with TiO2 as the dopant and Bi2MoO6 as the substrate, demonstrated significant versatility and potential for practical dye degradation applications.

Enhanced luminescence of Eu3+ doped β-PbF2 oxyfluoride glass ceramics for a new optical thermometry by charge compensation and local lattice symmetry breaking

Eu3+ doped β-PbF2 oxyfluoride glass ceramics (GCs) were synthesized via conventional melt-quenching method. The micro-morphology and luminescence properties of the fabricated GCs were characterized by X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM) and photoluminescence (PL) spectra. A new temperature sensing mechanism based on fluorescence intensity ratio (FIR) between 5D0 → 7FJ (1, 2, 3, 4) and 5D0 → 7F0 transitions of Eu3+ ion was proposed. Such new mechanism is due to strong thermal coupling of 7FJ (J = 0, 1, 2, 3, 4) states because of their small energy gap. With the increase of temperature, more and more population reaches high states 7FJ (J = 1, 2, 3, 4) from 7F0 state through thermalization process leading to different temperature-dependent transitions of 5D0 → 7FJ (J = 0, 1, 2, 3, 4). Furthermore, lattice distortion around Eu3+ ions caused by co-doped K+ ions resulting in distinct enhancement of emission of Eu3+ ion and violent splitting of 7FJ (J = 2, 3, 4) states. Meanwhile, narrowing of energy gap between 7FJ (J = 0, 1, 2, 3, 4) states resulting from the violent splitting of 7FJ (J = 2, 3, 4) states facilitated thermalization process between 7FJ (J = 0, 1, 2, 3, 4) states and then enhanced sensitivity of temperature measurement was obtained. We believe that this preliminary study will provide an important advance in exploring other innovative optical thermometry.

Effect of multi-walled carbon nanotubes on the visible light photocatalytic activity of AgInS2 for Rhodamine B degradation

Visible-light responsive AgInS2 (AIS) nanoparticles modified with either pristine multi-walled carbon nanotubes (p-MWCNTs) or mixed-acid (H2SO4 and HNO3) oxidized multi-walled carbon nanotubes (o-MWCNTs) were synthesized using a low-temperature liquid phase method. The resulting nanocomposites are denoted as p-MWCNTs/AIS or o-MWCNTs/AIS. The structure, morphology, and optical properties of the samples were characterized using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), high-resolution transmission electron microscopy (HRTEM), photoluminescence spectroscopy (PL), and ultraviolet-visible diffuse reflectance spectroscopy (UV–Vis DRS). The photocatalytic activity of p/o-MWCNTs/AIS towards the degradation of Rhodamine B (RhB) was investigated, and the optimal proportion of p/o-MWCNTs introduced on AIS was determined. A possible degradation mechanism of RhB over p/o-MWCNTs/AIS was proposed. The results demonstrated that p/o-MWCNTs were successfully incorporated into AIS, and the addition of an appropriate amount of p/o-MWCNTs improved the visible-light photocatalytic activity of AIS. Among the samples, 2 % o-MWCNTs/AIS exhibited the highest visible-light catalytic activity, achieving a degradation efficiency of 95 % within 40 min. The·⋅O2− species were identified as the main active species during the photocatalytic degradation process. The introduction of o-MWCNTs not only facilitated the separation of photogenerated electron-hole pairs (e−/h+) in AIS but also enhanced the visible-light absorption of AIS, leading to a significant improvement in its photocatalytic performance. Furthermore, the incorporation of o-MWCNTs greatly enhanced the cycling stability of AIS for reuse.

Dual-Functional Manganese-Doped ZnO-MOF Hybrid Material with Enhanced Hydrolytic Stability: A Fluorescent Photoinduced Electron Transfer Sensor for the Ultraselective Detection of Acetic Acid and Chromium (VI).

In recent years, the synthesis of metal-organic framework (MOF)─nanocomposites has received wide attention from the scientific fraternity due to the presence of a tunable hierarchical architecture and invasive versatility in applications. The present work focuses on the solvothermal synthesis of a novel hybrid MOF-nanocomposite through the impregnation of Mn-doped ZnO nanoparticles onto the matrix of a pioneer metal-organic framework that is composed of zinc metal connected with terephthalic acid linkers (MOF-5). The hierarchical arrangements of the prepared material were further assessed by Fourier-transform infrared spectroscopy (FTIR), powder X-ray diffraction (PXRD), high-resolution transmission electron microscopy (HR-TEM), UV-visible, photoluminescence (PL), and dynamic light scattering (DLS) measurements. The porosity analysis via nitrogen sorption measurements at 77 K showed that the material is porous with hierarchical micro-, wide micro-, and mesopores. The SAED pattern confirms the polycrystallinity of the material, which is in good agreement with the data obtained from PXRD analysis. Effective integration of Mn-doped ZnO onto the MOF structure was confirmed by XPS analysis, and the study further identified the oxidation state of the elements present. The synthesized analyte is an efficient fluorescent chemosensor for the detection of acetic acid, which can find further potential applications in intracellular imaging. Interestingly, the same compound also selectively detects the presence of Cr(VI) ions, thereby acting as a dual sensor, which finds applications in the sensing and removal of environmental contaminants. The material showed a sharp and intense emission at 569 nm at an excitation wavelength of 320 nm, and it exhibits high quenching efficiencies of 99.87 and 71.43% toward the sensing of μM level concentration of acetic acid and Cr2O72-, respectively. The highly efficient fluorescent sensing of pollutants, even at a shorter linear range, discarded the possibility of sensing the pollutants at higher concentration ranges. The Ksv value for the detection of acetic acid and Cr(VI) is found to be 3.7017 × 106 and 11.0324 × 106 M-1, respectively, which further confirms the higher sensing ability of the synthesized fluorophore. The mechanistic studies and density functional theory calculations of Mn-doped ZnO@MOF-5 reveal that photoinduced electron transfer plays a significant role in the turn-off response toward acetic acid and Cr2O72- ions. In the case of acetic acid, in addition to photoinduced electron transfer, hydrogen bonding interactions may also lead to fluorescence quenching. To the best of our knowledge, no precedent work has been reported for the sensing of acetic acid in the solution state. All other fluorescent sensing reports put forward the sensing and adsorption of acetic acid in the gaseous state, which makes this material a pioneer among others for the detection of acetic acid in the solution phase.

High-resolution photoluminescence study on donor-acceptor pair (DAP) recombination in silicon crystals co-doped with phosphorous and gallium

Before lower purity, lower cost silicon (Si) materials, such as compensated Si, can play a role in the terawatt-level (TW) capacity of photovoltaics, a better understanding of the fundamental properties of impurities in compensated Si is essential. In this work, high-resolution photoluminescence (PL) has been used to study the charge carrier radiative recombination through Donor-Acceptor pairs (DAPs) in phosphorus (P) and gallium (Ga) co-doped Si material grown for solar cell applications. The high spectral resolution of our PL system, 0.06 meV, enables us to overcome hitherto prior issues of overlapping spectral lines, giving access to extremely fine structures associated with DA pair (DAP) recombination. Our results confirm the presence of three broad bands and a discrete line structure related to DAP luminescence. The comparison of the discrete line structure due to DAPs recombination in the PL spectra with the theoretically predicted one allows the accurate determination of the Ga ionization energy. Temperature-dependent PL is then used to understand the thermally-induced changes in the DAP luminescence. In particular, we observe that the radiative recombination channel remains active for distant DAPs up to ∼40 K, unlike that for close-range DAPs for which the radiative channel is quenched after only slight increases in the temperature range 10–25 K. Furthermore, the analysis of the temperature dependent changes in the PL intensity of the broad DAP bands up to ∼200 K is used to derive the ionization energy of P donors in compensated Si material. In light of this important information, the significance of using high resolution PL to analyse spectral features in compensated Si is demonstrated.

A Unipolar Quantum Dot Diode Structure for Advanced Quantum Light Sources.

Triggered, indistinguishable single photons are crucial in various quantum photonic implementations. Here, we realize a novel n+-i-n++ diode structure embedding semiconductor quantum dots: the gated device enables spectral tuning of the transitions and deterministic control of the charged states. Blinking-free single-photon emission and high two-photon indistinguishability are observed. The line width's temporal evolution is investigated across over 6 orders of magnitude time scales, combining photon-correlation Fourier spectroscopy, high-resolution photoluminescence spectroscopy, and two-photon interference (visibility of VTPI,2ns = (85.8 ± 2.2)% and VTPI,9ns = (78.3 ± 3.0)%). Most of the dots show no spectral broadening beyond ∼9 ns time scales, and the photons' line width ((420 ± 30) MHz) deviates from the Fourier-transform limit by a factor of 1.68. The combined techniques verify that most dephasing mechanisms occur at time scales ≤2 ns, despite their modest impact. The presence of n-doping implies higher carrier mobility, enhancing the device's appeal for high-speed tunable, high-performance quantum light sources.

Correlative Imaging of Individual CsPbBr3 Nanocrystals: Role of Isolated Grains in Photoluminescence of Perovskite Polycrystalline Thin Films.

We report on the optical properties of a CsPbBr3 polycrystalline thin film on a single grain level. A sample composed of isolated nanocrystals (NCs) mimicking the properties of the polycrystalline thin film grains that can be individually probed by photoluminescence spectroscopy was prepared. These NCs were analyzed using correlative microscopy allowing the examination of structural, chemical, and optical properties from identical sites. Our results show that the stoichiometry of the CsPbBr3 NCs is uniform and independent of the NCs' morphology. The photoluminescence (PL) peak emission wavelength is slightly dependent on the dimensions of NCs, with a blue shift up to 9 nm for the smallest analyzed NCs. The magnitude of the blueshift is smaller than the emission line width, thus detectable only by high-resolution PL mapping. By comparing the emission energies obtained from the experiment and a rigorous effective mass model, we can fully attribute the observed variations to the size-dependent quantum confinement effect.

Study on the photoelectrocatalytic activity of reduced TiO2 nanotube films for removal of methyl orange

Abstract The reduced TiO2 film on which a photoelectrocatalytic (PEC) process had occurred was created from TiO2 nanotube film electrodes by the electrochemical reduction method. The obtained samples’ structure and morphology were characterized using UV-Vis diffuse reflectance spectroscopy, scanning electron microscopy, high-resolution transmission electron microscopy, photoluminescence, and X-ray diffraction. Cyclic voltammetry, linear sweep voltammetry, electrochemical impedance spectroscopy, chronoamperometry, UV-Vis absorbance spectroscopy, and Mott–Schottky plots were employed to examine the electrochemical and photoelectrochemical activities of the prepared electrodes. The results showed that the optimal conditions of cathodic polarization were a potential of −1.4 V for 60 min. The reduced TiO2 nanotube film electrode had better photoelectrochemical activities than pristine TiO2 under UV light due to the higher photocurrent density (13.7 mA‧cm−2) at 1.5 V (vs Ag/AgCl, sat. KCl reference electrode) compared to pristine TiO2 achieving 7.3 mA‧cm−2, indicating more effective charge separation and transport. The degradation of methyl orange (MO) on pristine TiO2 and reduced TiO2 electrodes was carried out in electrocatalytic (EC) and PEC conditions. The PEC process on the reduced TiO2 electrode had the highest MO processing efficiency (98.4%), and the EC process for MO removal on reduced TiO2 had higher efficiency (95.1%) than the PEC process on pristine TiO2 (89.2%).

Effect of Hydrothermal Conditions on Kenaf-Based Carbon Quantum Dots Properties and Photocatalytic Degradation

The development of biomass-based CQD is highly attentive to enhancing photocatalytic performance, especially in secondary or ternary heterogeneous photocatalysts by allowing for smooth electron-hole separation and migration. In this study, kenaf-based carbon quantum dots (CQD) were prepared. The main objective of the current work was to investigate temperature, precursor mass and time in hydrothermal synthesis treatment to improve the CQD properties and methylene blue photocatalytic degradation. Optimization of kenaf-based CQD for inclusion in hydrothermal treatment was analyzed. The as-prepared CQDs were characterized in detail by Fourier transform infrared (FTIR) spectroscopy, using a Hitachi TEM System (HT7830, RuliTEM, Tokyo, Japan), by photoluminescence (PL), and by ultraviolet-visible (UV-Vis) spectroscopy. It was found that C200-0.5-24 exhibits a higher photocatalytic activity of the methylene blue dye and optimized hydrothermal conditions of 200 °C, 0.5 g and 24 h. Therefore, novel kenaf-based CQD was synthesized for the first time and was successfully optimized in the as-mentioned conditions. During the hydrothermal treatment, precursor mass controls the size and the distribution of CQD nanoparticles formed. The C200-0.5-24 showed a clearly defined and well-distributed CQD with an optimized nanoparticle size of 8.1 ± 2.2 nm. Indeed, the C200-0.5-24 shows the removal rate of 90% of MB being removed within 120 min.

Dislocation reduction mechanism os GaN films on vicinal sapphire substrates

<sec>GaN materials are widely used in optoelectronic devices, high-power devices and high-frequency microwave devices because of their excellent characteristics, such as wide frequency band, high breakdown electric field, high thermal conductivity, and direct band gap. Owing to the large lattice mismatch and thermal mismatch brought by the heterogeneous epitaxy of GaN material, the GaN epitaxial layer will produce a great many dislocations in the growth process, resulting in the poor crystal quality of GaN material and the difficulty in further improving the device performance. Therefore, researchers have proposed the use of vicinal substrate to reduce the dislocation density of GaN material, but the dislocation annihilation mechanism in GaN film on vicinal substrate has not been sufficiently studied. Therefore, in this paper, GaN thin films are grown on vicinal sapphire substrates at different angles by using metal organic chemical vapor deposition technique. Atomic force microscope, high resolution X-ray diffractometer, photoluminescence testing, and transmission electron microscopy are used to analyze in detail the effects of vicinal substrates on GaN materials. The use of vicinal substrates can significantly reduce the dislocation density of GaN materials, but lead to degradation of their surface morphology morphologies. And the larger the substrate vicinal angle, the lower the dislocation density of the sample is. The dislocation density of the sample with a 5º bevel cut on the substrate is reduced by about one-third compared to that of the sample with a flat substrate. The special dislocation termination on the mitered substrate is observed by transmission electron microscopy, which is one of the main reasons for the reducing the dislocation density on the mitered substrate. The step merging on the vicinal sapphire substrate surface leads to both transverse growth and longitudinal growth of GaN in the growth process. The transverse growth region blocks the dislocations, resulting in an abrupt interruption of the dislocations during propagation, which in turn reduces the dislocation density.</sec><sec>Based on the above phenomena, a model of GaN growth on vicinal substrate is proposed to explain the reason why the quality of GaN crystal can be improved by vicinal substrate.</sec>

Analysis of site symmetries of Er3+ doped CaF2 and BaF2 crystals by high resolution photoluminescence spectroscopy

The understanding of complex relationships between luminescent properties, local symmetry of an emitting center, and the host crystal structure provides a better insight into optical properties of materials. In this work, the alkaline earths CaF2 and BaF2 fluoride crystals doped with 0.1 mol% ErF3 were investigated. The crystals structure has been studied using a synchrotron and laboratory X-ray diffraction. The C3v and C4v sites symmetry were determined using erbium probed high resolution emission spectroscopy (HRPL) at low temperature (LT) of 10 K. The considerable difference in room temperature (RT) optical properties for CaF2 compared to BaF2 crystals was observed. Such difference in absorption intensity of 4.7 times of erbium 4G11/2 manifold in UV, and 7.5 times in green emission from 4S3/2 manifold, could be due to the distinction in the host crystals cationic radius (ΔrCa,Ba) and the dopant-host ionic radius (ΔrCa-Er, ΔrBa-Er). Those Δr differences influence the structure and lead to the following symmetry formation: In CaF2, the C4v and C3v isolated centers were identified, with the determined Er3+- F−i bond lengths of 2.734 Å and 4.735 Å respectively; In BaF2, only C3v isolated centers were identified with the determined Er3+- F−i bond lengths of 5.380 Å. The present work is the first study that takes into account correlations of optical properties, the local symmetry and the structure in mentioned fluorides crystals, and it could be a step forward in the lanthanide doped optical materials systematics.

Effects of the diameter of thermally generated nanopits on carrier dynamics in AlGaN/GaN heterostructures

The size and density of nanopits, generated at the surface of their top layer, strongly affect the electrical and optical properties of AlGaN-based structures. Therefore, the control of the layer quality evolution as a function of the nanopits size/density is a crucial issue to enhance the device performance. In this paper, the effects of the nanopits diameter observed at the surface of AlGaN on carrier dynamics are systematically investigated. The variation of nanopits diam-eter is achieved through thermal annealing of a set of AlGaN/GaN heterostructures at different temperatures. The samples are characterized using the scanning electron microscope (SEM), energy-dispersive x-ray, high-resolution x-ray diffraction, photoluminescence (PL), and time-resolved PL spectroscopies. SEM images have revealed an increase in the nanopits diameter with increasing annealing temperature. In addition, we observed a linear development in the yellow luminescence intensity, accompanied by a deterioration in the PL decay times due to an increase in the density of point-defect complexes that act as nonradiative recombination centers. We also performed temperature-dependent PL measurements to study the impact of the nanopits diameter on electron–phonon scattering processes. Both electron-acoustic- and electron-longitudinal optical phonon interactions enhance with increasing nanopits diameter.

Disorder and wave-function intermixing effects in the luminescence spectra of LiYF4:Ho in external magnetic fields

On the basis of the high-resolution low-temperature photoluminescence spectra of LiYF4:Ho crystals we discuss spectral manifestations of disorder caused by random distribution of either the lithium isotopes or defects in the crystal lattice. A peculiar discrete spectral structure of a different nature was found in the magnetic-field-dependent spectra. We show that it arises due to mixing of the wave functions at the anticrossings of hyperfine levels in a magnetic field.

Exhaustive characterization of modified Si vacancies in 4H-SiC

Abstract The negatively charged silicon vacancy V S i − $\left({\mathrm{V}}_{\mathrm{S}\mathrm{i}}^{-}\right)$ in silicon carbide is a well-studied point defect for quantum applications. At the same time, a closer inspection of ensemble photoluminescence and electron paramagnetic resonance measurements reveals an abundance of related but so far unidentified signals. In this study, we search for defects in 4H-SiC that explain the above magneto-optical signals in a defect database generated by automatic defect analysis and qualification (ADAQ) workflows. This search reveals only one class of atomic structures that exhibit silicon-vacancy-like properties in the data: a carbon antisite (CSi) within sub-nanometer distances from the silicon vacancy only slightly alters the latter without affecting the charge or spin state. Such a perturbation is energetically bound. We consider the formation of V S i − + C S i ${\mathrm{V}}_{\mathrm{S}\mathrm{i}}^{-}+{\mathrm{C}}_{\mathrm{S}\mathrm{i}}$ up to 2 nm distance and report their zero phonon lines and zero field splitting values. In addition, we perform high-resolution photoluminescence experiments in the silicon vacancy region and find an abundance of lines. Comparing our computational and experimental results, several configurations show great agreement. Our work demonstrates the effectiveness of a database with high-throughput results in the search for defects in quantum applications.

Non-invasive and non-destructive characterization of MBE-grown CdZnTe/CdTe superlattice-based dislocation filtering layers

We report on the structural and optical properties of heteroepitaxial II–VI CdTe (211)B buffer layers with strained CdZnTe/CdTe superlattice layers, investigated by employing non-destructive methods including high-resolution x-ray diffraction, cathodoluminescence, and photoluminescence spectroscopy. X-ray diffraction reciprocal space mapping measurements revealed that the superlattice layers are coherently strained, leading to a spread in x-ray double-crystal rocking curve full-width at half-maximum values but better in-plane lattice-matching with HgCdTe. Both cross-sectional cathodoluminescence and photoluminescence measurements confirm the coherent growth of superlattice layers and their dislocation filtering effects. Both these techniques in CdTe layers are found to be well correlated with the dislocation density as determined by etch pit density measurements. The results indicate the potential of these non-destructive methods to be further developed into general-purpose techniques capable of characterizing the defect evolution in semiconductor heteroepitaxy.