Paramagnetism in Microwave-Synthesized Metal-Free Nitrogen-Doped Graphene Quantum Dots.

Nitrogen-doped graphene quantum dots (NGQDs) have gained significant attention due to their various physical and chemical properties; however, there is a gap in the study of NGQDs' magnetic properties. This work adds to the efforts of bridging the gap by demonstrating the room temperature paramagnetism in GQDs doped with Nitrogen up to 3.26 at.%. The focus of this experimental work was to confirm the paramagnetic behavior of metal free NGQDs resulting from the pyridinic N configuration in the GQDs host. Metal-free nitrogen-doped NGQDs were synthesized using glucose and liquid ammonia as precursors by microwave-assisted synthesis. This was followed by dialysis filtration. The morphology, optical, and magnetic properties of the synthesized NGQDs were characterized carefully through atomic force microscopy (AFM), transmission electron microscopy (TEM)), UV-VIS spectroscopy, fluorescence, X-ray photon spectroscopy (XPS), and vibrating sample magnetometer (VSM). The high-resolution TEM analysis of NGQDs showed that the NGQDs have a hexagonal crystalline structure with a lattice fringe of ~0.24 nm of (1120) graphene plane. The N1s peak using XPS was assigned to pyridinic, pyrrolic, graphitic, and oxygenated NGQDs. The magnetic study showed the room-temperature paramagnetic behavior of NGQDs with pyridinic N configuration, which was found to have a magnetization of 20.8 emu/g.

Ellipsometry Study of CdSe Thin Films Deposited by PLD on ITO Coated Glass Substrates.

Cadmium selenide (CdSe) thin films were deposited on indium tin oxide (ITO) coated glass substrates using pulsed laser deposition (PLD) technique under different growth temperatures. Samples were investigated for their structural, morphological, and optical properties through X-ray diffraction (XRD), atomic force microscopy (AFM), and UV-Vis-NIR spectroscopy. AFM analysis revealed that the surface roughness of the as-grown CdSe thin films increased with the increase in deposition temperature. The optical constants and film thickness were obtained from spectroscopic ellipsometry analysis and are discussed in detail. The optical band gap of the as-grown CdSe thin films, calculated from the Tauc plot analysis, matched with the ellipsometry measurements, with a band gap of ~1.71 eV for a growth temperature range of 150 °C to 400 °C. The CdSe thin films were found to have a refractive index of ~3.0 and extinction coefficient of ~1.0, making it a suitable candidate for photovoltaics.

Magnetic Control of the Manganese Photoluminescence in Fe3O4/l-Cys ZnS:Mn Nanocomposites.

We investigated the magnetic control of the Mn photoluminescence (PL) in iron oxide/l-cysteine-capped zinc sulfide (Fe3O4/l-cys ZnS:Mn) nanocomposites via temperature- and field-dependent PL intensity studies. Fe3O4/l-cys ZnS:Mn was synthesized following a wet chemical deposition route and then its physicochemical, morphological, and magnetic properties were characterized. X-ray diffraction analysis indicates the formation of a semiconducting composite material with coexisting phases with high crystalline quality and purity. Electron microscopy reveals that the surfaces of the nanoparticles are clean and smooth, sized between 15 and 30 nm, without any sheathed amorphous phase. Vibrating sample magnetometry and UV light excitation show a clear superparamagnetic behavior and an optical response of Fe3O4/l-cys ZnS:Mn, which revealed its bifunctional nature. Magnetoluminescent coupling at 1.0 T is seen in the form of PL suppression in Fe3O4/l-cys ZnS:Mn from low temperature (10 K) to room temperature, with a PL intensity drop of ∼5% at 10 K and a maximum drop of 10% at room temperature. This observation can be explained by restriction of the energy transfer to Mn orbitals through magnetic ordering and Jahn-Teller distortions. Fe3O4/l-cys ZnS:Mn shows promise as a bifunctional biocompatible compound that can be applied as a theranostic agent and a quantum computational element. A deeper understanding behind the magnetic control of the optical response in bifunctional materials brings forth new arenas in diagnostics and drug delivery.

Synthesis, Characterization and Fabrication of Graphene/Boron Nitride Nanosheets Heterostructure Tunneling Devices.

Various types of 2D/2D prototype devices based on graphene (G) and boron nitride nanosheets (BNNS) were fabricated to study the charge tunneling phenomenon pertinent to vertical transistors for digital and high frequency electronics. Specifically, G/BNNS/metal, G/SiO2, and G/BNNS/SiO2 heterostructures were investigated under direct current (DC-bias) conditions at room temperature. Bilayer graphene and BNNS were grown separately and transferred subsequently onto the substrates to fabricate 2D device architectures. High-resolution transmission electron microscopy confirmed the bilayer graphene structure and few layer BNNS sheets having a hexagonal B3-N3 lattice. The current vs voltage I(V) data for the G/BNNS/Metal devices show Schottky barrier characteristics with very low forward voltage drop, Fowler-Nordheim behavior, and 10-4 Ω/sq. sheet resistance. This result is ascribed to the combination of fast electron transport within graphene grains and out-of-plane tunneling in BNNS that circumvents grain boundary resistance. A theoretical model based on electron tunneling is used to qualitatively describe the behavior of the 2D G/BNNS/metal devices.

T1- and T2-weighted Magnetic Resonance Dual Contrast by Single Core Truncated Cubic Iron Oxide Nanoparticles with Abrupt Cellular Internalization and Immune Evasion.

Conventional T1- or T2-weighted single mode contrast-enhanced magnetic resonance imaging (MRI) may produce false results. Thereby, there is a need to develop dual contrast agents, T1- and T2-weighted, for more accurate MRI imaging. The dual contrast agents should possess high magnetic resonance (MR) relaxivities, targeted tumor linking, and minimum recognition by the immune system. We have developed nitrodopamine-PEG grafted single core truncated cubic iron oxide nanoparticles (ND-PEG-tNCIOs) capable of producing marked dual contrasts in MRI with enhanced longitudinal and transverse relaxivities of 32 ± 1.29 and 791 ± 38.39 mM-1 s-1, respectively. Furthermore, the ND-PEG-tNCIOs show excellent colloidal stability in physiological buffers and higher cellular internalization in cancerous cells than in phagocytic cells, indicating the immune evasive capability of the nanoparticles. These findings indicate that tNCIOs are strong candidates for dual contrast MRI imaging, which is vital for noninvasive real-time detection of nascent cancer cells in vivo and for monitoring stem cells transplants.

Effect of laser speckle on light from laser diode-pumped phosphor-converted light sources.

Laser diode (LD) pumped white light sources are being developed as an alternative to light-emitting diode-pumped sources for high efficiency and/or high brightness applications. While several performance metrics of laser-pumped phosphor-converted light sources have been investigated, the effect of laser speckle has not been sufficiently explored. This paper describes our experimental studies on how laser speckle affects the behavior of light from laser-excited phosphor lamps. A single LD pumping a phosphor plate was the geometry explored in this work. Overall, our findings are that the down-converted light did not exhibit any speckle, whereas speckle was present in the residual pump light but much reduced from that in direct laser light. Furthermore, a thicker coating of small-grained phosphors served to effectively reduce speckle through static pump light diffusion in the phosphor coating. Our investigations showed that speckle is not of concern in illumination from LD-pumped phosphor-converted light sources.

Preparation of balanced trichromatic white phosphors for solid-state white lighting.

High quality white light-emitting diodes (LEDs) employ multi-component phosphor mixtures to generate light of a high color rendering index (CRI). The number of distinct components in a typical phosphor mix usually ranges from two to four. Here we describe a systematic experimental technique for starting with phosphors of known chromatic properties and arriving at their respective proportions for creating a blended phosphor to produce light of the desired chromaticity. This method is applicable to both LED pumped and laser diode (LD) pumped white light sources. In this approach, the radiometric power in the down-converted luminescence of each phosphor is determined and that information is used to estimate the CIE chromaticity coordinate of light generated from the mixed phosphor. A suitable method for mixing multi-component phosphors is also described. This paper also examines the effect of light scattering particles in phosphors and their use for altering the spectral characteristics of LD- and LED-generated light. This is the only approach available for making high efficiency phosphor-converted single-color LEDs that emit light of wide spectral width.

Laser-driven phosphor-converted white light source for solid-state illumination.

Energy efficiency and lighting quality considerations are driving research into laser-pumped white light sources. Laser diodes as pump sources for downconversion phosphors promise freedom from "droop" that adversely affects the efficiency of light-emitting diodes (LEDs). High-intensity laser diode-pumped light sources for applications such as search lights and automobile headlights have been demonstrated recently. Our paper describes the design and construction of a domestic/office-type solid-state luminaire driven by light from an integrated violet laser-diode module. A trichromatic phosphor made from a blend of separate europium-containing rare-earth phosphors was used as the downconversion medium. Mechanical and optical design of the reflector and the phosphor plate are described. Characteristics of both the pump light and the downconverted light are also described. Our studies also looked at the variation of chromaticity coordinates with variation in pump power and the effect of laser speckle on the lamp's light output. Finally, there is a brief discussion of energy conversion efficiency and longevity considerations, comparing pumping with LEDs versus pumping with laser diodes.

Novel magneto-luminescent effect in LSMO/ZnS:Mn nanocomposites at near-room temperature.

We report the tuning of the internal Mn photoluminescence (PL) transition of magnetically-ordered Sr-doped lanthanum manganite (LSMO)/Mn-doped zinc sulfide (ZnS:Mn) nanocomposites (NCs) by applying a static magnetic field in the range of 0-1 T below the critical temperature of ∼225 K. To do that, we have systematically fabricated LSMO/ZnS:Mn at different concentrations (1:1, 1:3, 1:5 and 1:10 wt%) via a straightforward solid-state reaction. X-ray diffraction and Raman analyses reveal that both phases coexist with a high degree of crystallinity and purity. Electron microscopy indicates that the NCs are almost spherical with an average crystal size of ∼6 nm, and that their surfaces are clean and smooth. The bifunctional character of LSMO/ZnS:Mn was evidenced by vibrating sample magnetometry and PL spectroscopy analyses, which show a marked ferromagnetic behavior and a broad, intense Mn orange emission band at room temperature. Moreover, the LSMO/ZnS:Mn at 1:3 wt% exhibits magneto-luminescent (ML) coupling below 225 K, and reaches the largest suppression of Mn-band PL intensity (up to ∼10%) at 150 K, when a magnetic field of 1.0 T is applied. The ML effect persists at magnetic fields as low as 0.2 T at 8 K, which can be explained by evoking a magnetic-ordering-induced spin-dependent restriction of the energy transfer to Mn states. No ML effect was observed in bare ZnS:Mn nanoparticles under the same experimental parameters. Our findings suggest that this NC can be considered as a new ML compound, similar to FeCo/InGaN-GaN and LSMO/ZnO NCs, useful as q-bits for quantum computation. The results presented here bring forth new avenues to better understand the interaction between semiconductors and perovskites, and exploit their synergistic effects in magneto-optics, spintronics and nanoelectronics.

Nanoscale structure study of boron nitride nanosheets and development of a deep-UV photo-detector.

In this communication, we report on the synthesis of few atomic-layer boron nitride nanosheets (BNNSs) and their application for deep ultraviolet photo-detection. Synthesis of BNNSs is carried out by using the short-pulse plasma beam deposition technique. High-resolution tunneling electron microscopy, cathodoluminescence spectroscopy and photo-stimulated measurements are conducted and linked to characterize the BNNS morphology. The obtained BNNSs are flat with a typical size of 50 × 50 µm(2) and are optically transparent down to 210 nm. Nanoscale studies by transmission electron microscopy revealed that these nanosheets are composed of a densely packed honeycomb crystal lattice structure of covalently bonded boron and nitrogen atoms. Cathodoluminescence spectroscopy of these nanosheets revealed a single sharp excitonic peak centered at 233 nm at 300 K. The synthesized BNNSs are used to demonstrate applicability of BNNSs for detecting ultraviolet photons. The initial experimental tests of the developed prototype BNNSs based deep-ultraviolet photo-detector show that it is blind to photons with an energy less than 4 eV. The calculated output power of the detector is approximately 2 µW and the ratio between the output electrical power and the input optical power is ∼1%.

Single-crystal γ-MnS nanowires conformally coated with carbon.

We report for the first time the fabrication of single-crystal metastable manganese sulfide nanowires (γ-MnS NWs) conformally coated with graphitic carbon via chemical vapor deposition technique using a single-step route. Advanced spectroscopy and electron microscopy techniques were applied to elucidate the composition and structure of these NWs at the nanoscale, including Raman, XRD, SEM, HRTEM, EELS, EDS, and SAED. No evidence of α-MnS and ß-MnS allotropes was found. The γ-MnS/C NWs have hexagonal cross-section and high aspect ratio (∼1000) on a large scale. The mechanical properties of individual γ-MnS/C NWs were examined via in situ uniaxial compression tests in a TEM-AFM. The results show that γ-MnS/C NWs are brittle with a Young's modulus of 65 GPa. The growth mechanism proposed suggests that the bottom-up fabrication of γ-MnS/C NWs is governed by vapor-liquid-solid mechanism catalyzed by bimetallic Au-Ni nanoparticles. The electrochemical performance of γ-MnS/C NWs as an anode material in lithium-ion batteries indicates that they outperform the cycling stability of stable micro-sized α-MnS, with an initial capacity of 1036 mAh g(-1) and a reversible capacity exceeding 503 mAh g(-1) after 25 cycles. This research advances the integration of carbon materials and metal sulfide nanostructures, bringing forth new avenues for potential miniaturization strategies to fabricate 1D core/shell heterostructures with intriguing bifunctional properties that can be used as building blocks in nanodevices.