Ni doping induced property enhancement in laser ablated BaSnO3 films suitable for optoelectronic applications.

Pulsed laser deposition is a straightforward approach for preparing films with superconducting to dielectric properties with atomic layer precision. The deep-seated mechanisms involved in the particle transport from target to substrate and subsequent film formation still need to be fully comprehended. This manuscript reports the property enhancement observed in laser ablated perovskite BaSnO3 films with Ni doping. Films' crystallinity improvement is observed, and an intensity enhancement of 1150% is observed on 3 mol% Ni-doping. The optimum Ni-doping concentration in BaSnO3 is found to be 3 mol%. Herein, Ni-doped BaSnO3 films deposited by PLD showed an unusual increase in film thickness (i.e., from 615 nm in the pure film to 1317 nm in the film with 7 mol% Ni-doping as revealed by lateral SEM analysis and spectroscopic ellipsometry). We propose an "Induced Magnetic field-assisted Particle Convergence (IMPC)" effect for this superficial growth enhancement. The film's optical properties are modified with an increased nickel doping level, and the bandgap energy shows renormalization. All the films show excellent transmittance (80-90%) in the Vis.-NIR region. Hall-effect measurement reveals the increased carrier concentration by three orders (2.98 × 1011 to 3.50 × 1014 cm-3). In addition, the enhancement in mobility from 3.13 to 20.93 cm2V-1s-1 and a decrease in electrical resistivity by six orders (i.e., from 4.05 × 109 to 1.13 × 103 Ω cm) are observed on 7 mol% Ni doping. XPS measurements reveals that the Ba, Sn and Ni ions are at 2+, 4+ and 2+ oxidation states. Using spectroscopic ellipsometric method, we estimated the optical constants of the films, the refractive index, dielectric constant, and extinction coefficient show a normal dispersion behavior. The high crystallinity, high transmittance, suitable surface topography, and improved electrical performances of the Ni-doped BaSnO3 films make them excellent candidates for optoelectronic devices and solar cells.

Tailoring the Emission Behavior of WO3 Thin Films by Eu3+ Ions for Light-Emitting Applications.

The article reports the successful fabrication of Eu3+-doped WO3 thin films via the radio-frequency magnetron sputtering (RFMS) technique. To our knowledge, this is the first study showing the tunable visible emission (blue to bluish red) from a WO3:Eu3+ thin film system using RFMS. X-ray diffractograms revealed that the crystalline nature of these thin films increased upto 3 wt% of the Eu3+ concentration. The diffraction peaks in the crystalline films are matched well with the monoclinic crystalline phase of WO3, but for all the films', micro-Raman spectra detected bands related to WO3 monoclinic phase. Vibrational and surface studies reveal the amorphous/semi-crystalline behavior of the 10 wt% Eu3+-doped sample. Valence state determination shows the trivalent state of Eu ions in doped films. In the 400-900 nm regions, the fabricated thin films show an average optical transparency of ~51-85%. Moreover, the band gap energy gradually reduces from 2.95 to 2.49 eV, with an enhancement of the Eu3+-doping content. The doped films, except the one at a higher doping concentration (10 wt%), show unique emissions of Eu3+ ions, besides the band edge emission of WO3. With an enhancement of the Eu3+ content, the concentration quenching process of the Eu3+ ions' emission intensities is visible. The variation in CIE chromaticity coordinates suggest that the overall emission color can be altered from blue to bluish red by changing the Eu3+ ion concentration.

Sm3+-doped strontium barium borate phosphor for white light emission: Spectroscopic properties and Judd-Ofelt analysis.

This study aims to explore the spectroscopic properties of a Sr1.0Ba2.0B6O12:0.5Sm3+ phosphor synthesized using the solid-state reaction method. The morphology and elemental composition of the phosphor were determined using scanning electron microscopy and energy-dispersive X-ray spectroscopy, respectively. Phase changes and crystallite phases in the phosphor were studied using differential-scanning calorimetry and X-ray diffraction, respectively. Raman and Fourier-transform infrared spectra were used to identify the molecular vibrations in the phosphor. The energy bandgap and bonding nature of the phosphor were analyzed using the absorption spectrum. The nephelauxetic ratios determined from the absorption peaks revealed the presence of both ionic and covalent bonding in the phosphor. Judd-Ofelt parameters, along with radiative properties of the phosphor, were evaluated using the peaks in the absorption spectrum. Colorimetric analysis using the photoluminescence spectrum showed that the Sr1.0Ba2.0B6O12:0.5Sm3+ phosphor emits a cool-white light. The higher values of the spectroscopic quality factor, stimulated-emission cross-section, quantum efficiency, and the white-light emission of the phosphor suggest that Sr1.0Ba2.0B6O12:0.5Sm3+ is useful for display and lighting applications.

Simultaneous detection of different probe molecules using silver nanowires as SERS substrates.

Metallic silver nanowires with high yield were synthesized using a modified seed mediated approach at room temperature. Ribbon-like nanostructures were obtained when the concentration of NaOH was lower and further increase of NaOH transformed it into long nanowires. These nanowires possess high aspect ratio, with length and diameter ~6.5 µm and 17 nm respectively. The surface enhanced Raman scattering activity of these nanowires was tested with three different probe molecules viz., crystal violet, malachite green and nile blue chloride using visible (514.4 nm) and near-infrared (784.8 nm) excitation lines. The minimum detection limits for crystal violet and nile blue chloride molecules were found to be down to 10-7 M with good linear responses, as evidenced by values of correlation coefficients, indicating their potential for a variety of applications such as sensing. Principal component analysis was performed with the surface enhanced Raman spectra in order to discriminate the dye molecules and their mixture, simultaneously. The first two principal components, which provided 69.80 and 27.93% of the total data variance, could be conveniently represented as a two dimensional PCA score plot. The score plot showed clear clustering of probe molecules and their mixture. The relative contribution of wavenumbers to each of the two principal components was identified by plotting the PCA loading matrix. These results further promote possibilities of quantification of multiplexed SERS detection and analysis.

Plasmonic photocatalytic activity of ZnO:Au nanostructures: Tailoring the plasmon absorption and interfacial charge transfer mechanism.

ZnO:Au nanostructures with tunable surface Plasmon band were synthesizedvia co-precipitation method. X-ray diffraction analysis, high resolution transmission electron microscopy and Raman spectra confirmed the hexagonal wurtzite phase for these ZnO:Au nanostructures with preferential growth along the (101) plane. The selective enhancement in the intensity of Raman band due to the excited free electrons of Au nanoparticles confirmed the incorporation of Au in ZnO matrix. Scanning electron microscopic images showed the transformation of morphology of these nanostructures from rod geometry to rose flower and then to marigold flower-like structures with increase in the Au content. Detailed investigations were carried out to understand the role of plasmons present in the ZnO:Au nanostructures on the photocatalytic degradation of sulforhodamine B under sunlight. It is found that ZnO:Au nanostructures with plasmon band in the close approximation of solar maximum ˜550 nm as catalysts exhibit ultra-fast degradation of the dye. This highly efficient photocatalytic activity of these nanostructures is attributed to the electron scavenging action of Au due to its high electronegativity, enhanced absorption of sunlight due to plasmons, the enhanced surface area of ZnO:Au nanostructures and the formation of Schottky barrier between the Au and ZnO interface. The reusability and photostability of these catalysts were tested through repetitive cycles and demonstrated that these nanostructures can form excellent reusable photocatalysts for the degradation of toxic organic waste in water.

Au-Ag hollow nanostructures with tunable SERS properties.

Fabrication of hollow Au-Ag nanoparticles is done by the sequential action of galvanic replacement and Kirkendall effect. Polyol synthesized silver nanoparticles were used as templates and the size of cavities is controlled by the systematic addition of the HAuCl4. Au-Ag nanoparticles carved in different depths were tested for application as substrates for surface enhanced Raman scattering. Two medically important Raman active analytes-Nile blue chloride and Crystal violet were used in the surface enhanced Raman scattering (SERS) performance analysis. A systematic study has been made on the Raman enhancement of hollow nanoparticles fabricated with different cavity dimensions and compared with that of the silver templates used. The enhancement observed for these hollow substrates with cavities is of interest since Au protected hollow nanostructures are vital and an active area of interest in drug delivery systems.

Ag@Au core-shell nanoparticles synthesized by pulsed laser ablation in water: Effect of plasmon coupling and their SERS performance.

Ag@Au core-shell nanoparticles are synthesised by pulsed laser ablation in water using low energy laser pulses. The plasmon characteristics of these core-shell nanoparticles are found to be highly sensitive to the thickness of Au coating. In the synthesis, at first silver nanocolloid was prepared by ablating Ag target and then it is followed by ablation of Au target for different time durations to form Ag@Au core-shell nanostructures. The effect of plasmon-plasmon coupling on the absorption spectra is investigated by decreasing the effective distance between the nanoparticles. This is achieved by reducing the total volume of the colloidal suspension by simple evaporation of water, the solvent used. The suitability of these core-shell nanostructures for application as surface enhanced Raman scattering substrates are tested with crystal violet as probe molecules. Influence of plasmon coupling on the enhancement of Raman bands is found to be different for different bands.

Surface enhanced Raman scattering, antibacterial and antifungal active triangular gold nanoparticles.

Shape controlled syntheses of gold nanoparticles have attracted a great deal of attention as their optical, electronic, magnetic and biological properties are strongly dependent on the size and shape of the particles. Here is a report on the surface enhanced Raman scattering (SERS) activity of Cinnamomum zeylanicum leaf broth reduced gold nanoparticles consisting of triangular and spherical like particles, using 2-aminothiophenol (2-ATP) and crystal violet (CV) as probe molecules. Nanoparticles prepared with a minimum leaf broth concentration, having a greater number of triangular like particles exhibit a SERS activity of the order of 10(7). The synthesized nanoparticles exhibit efficient antibacterial activity against the tested gram negative bacterium Escherichia coli and gram positive bacterium Staphylococcus aureus. Investigations on the antifungal activity of the synthesized nanoparticles against Aspergillus niger and Fusarium oxysporum positive is also discussed.

Gold nanorods with finely tunable longitudinal surface plasmon resonance as SERS substrates.

Advances in nanophotonics have shown the potential of colloidal metal nanoparticles with sharp tips, such as rods, to focalize plasmonic electromagnetic fields. We report on the synthesis of Au nanorods via a seed mediated approach and the influence of silver ions on the aspect ratio of the Au nanorods. The longitudinal surface plasmon resonance (LSPR) of the Au nanorods was successfully tuned with the concentration of silver ions. The surface enhanced Raman scattering (SERS) effect of 2-aminothiophenol (2-ATP) as a probe molecule on Au nanorods was systematically studied by varying the longitudinal surface plasmon resonance of the nanorods. The highest electromagnetic enhancement was observed when the longitudinal surface plasmon resonance of the Au nanorods overlapped with the laser excitation wavelength. The variation of the SERS enhancement factor with the longitudinal surface plasmon resonance and laser excitation lines is also discussed in detail.

Green synthesis of gold nanoparticles using Cinnamomum zeylanicum leaf broth.

Development of biologically inspired experimental processes for the synthesis of nanoparticles is an important branch of nanotechnology. The synthesis of gold nanoparticles using Cinnamomum zeylanicum leaf broth as the reducing agent is reported. The morphology of the particles formed consists of a mixture of gold nanoprisms and spheres with fcc (111) structure of gold. At lower concentrations of the extract, formation of prism shaped Au particles dominates, while at higher concentrations almost spherical particles alone are observed. Good crystallinity of the nanoparticles with fcc phase is evident from XRD patterns, clear lattice fringes in the high resolution TEM image and bright circular rings in the SAED pattern. Au nanoparticles grown are observed to be photoluminescent and the intensity of photoemission is found to increase with increase in leaf broth concentration. The ability to modulate the shape of nanoparticles as observed in this study for gold nanoparticles opens up the exciting possibility of developing further synthetic routes employing ecofriendly sources.

Aqueous synthesis and characterization of CdS, CdS:Zn(2+) and CdS:Cu(2+) quantum dots.

CdS quantum dots of different sizes approximately 3-5nm were prepared using aqueous solutions of CdSO(4) and Na(2)S(2)O(3) at 303K with thioglycerol as stabilizing agent and catalyst. The broad X-ray diffraction pattern and SAED pattern with bright circular spots and clear lattice fringes in the high-resolution TEM image indicate cubic phase of the nanocrystals. Band gap changes from the bulk value of 2.4 to 3.16eV in the nanoparticles indicating quantum size effect. The photoluminescence (PL) spectrum is blue-shifted to 528nm. The PL emission band is blue/red-shifted on doping with Zn(2+)/Cu(2+). In the case of Cu(2+), the PL intensity is found to be maximum at 10wt% doping and almost completely quenched at 15wt% doping. On doping with Zn(2+), the intensity and blue-shift of PL are found to be maximum at 2 and 6wt% doping, respectively.

Studies on optical absorption and photoluminescence of thioglycerol-stabilized CdS quantum dots.

Nanoparticles of CdS were prepared at 303 K by aqueous precipitation method using CdSO4 and (NH4)2S in presence of the stabilizing agent thioglycerol. Adjustment of the thioglycerol (T) to ammonium sulphide (A) ratio (T:A) from 1:25 to 1:3.3 was done during synthesis and nanoparticles of different size were obtained. The prepared colloids were characterized by UV-vis and photoluminescence (PL) spectroscopic studies. Prominent first and second excitonic transitions are observed in the UV-vis spectrum of the colloid prepared with a T:A ratio of 1:3.3. Particle size analysis was done using XRD, high resolution TEM and dynamic light scattering and found to be approximately 3 nm. UV-vis and PL spectral features also agree with this particle size in colloid with T:A of 1:3.3. The band gap of CdS quantum dots has increased from the bulk value 2.4-2.9 eV. PL spectra show quantum size effect and the peak is shifted from 628 to 556 nm when the ratio of T:A was changed from 1:25 to 1:3.3. Doping of CdS with Zn2+ and Cu2+ is found to enhance the PL intensity. PL band shows blue-shift and red-shift on doping with Zn2+ and Cu2+, respectively. UV and PL spectral features of the CdS/Au hybrid nanoparticles obtained by a physical mixing of CdS and Au nanoclusters in various volume ratios is also discussed. Au red-shifts and rapidly quenches the PL of CdS. An additional low energy band approximately 650 nm is observed in the UV visible spectrum of the hybrid nanoparticles.

Studies on surface plasmon resonance and photoluminescence of silver nanoparticles.

Silver nanoparticles of different sizes were prepared by citrate reduction and characterized by UV-vis absorbance spectra, TEM images and photoluminescence spectra. The morphology of the colloids obtained consists of a mixture of nanorods and spheres. The surface plasmon resonance (SPR) and photoemission properties of Ag nanoparticles are found to be sensitive to citrate concentration. A blue shift in SPR and an enhancement in photoluminescence intensity are observed with increase in citrate concentration. Effect of addition of KCl and variation of pH in photoluminescence was also studied.

Synthesis, characterization and SERS activity of Au-Ag nanorods.

The formation mechanism and morphology of Au-Ag bimetallic colloidal nanoparticles depend on the composition. Ag coated Au colloidal nanoparticles have been prepared by deposition of Ag through chemical reduction on performed Au colloid. The composition of the Au100-x-Agx particles was varied from x=0 to 50. The obtained colloids were characterized by UV-vis spectroscopy and transmission electron microscopy (TEM). The Au80-Ag20 colloid consists of alloy nanorods with dimension of 25nm x 100nm. The activity of these nanorods in surface enhanced Raman spectroscopy (SERS) was checked by using sodium salicylate as an adsorbate probe. Intense SERS bands are observed indicating its usefulness as a SERS substrate in near infrared (NIR) laser excitation.