RÉSUMÉ
Surface-enhanced Raman scattering is a practical, noninvasive spectroscopic technique that measures chemical fingerprints for varieties of molecules in multiple applications. However, synthesizing appropriate substrates for practical, long-term applications of this method has always been a challenging task. In the present study, we show that ZnO/Ag nanohybrid substrates may act as highly stable, sensitive, and recyclable substrates for surface-enhanced Raman scattering, as illustrated by the detection of methylene blue, selected as a test dye molecule with self-cleaning functionalities. Specifically, we demonstrate the detection enhancement factor of 3.7 × 107 along with exceptional long-term stability explained in terms of the localized surface plasmon resonance from the Ag nanocrystals embedded into the chemically inert ZnO nanoparticles, constituting the nanohybrid. Significantly, these substrates can be efficiently cleaned and regenerated while maintaining their high performance upon recycling. As a result, using these substrates, up to 10-12 M detection sensitivity has been demonstrated, enabling the accuracy required in modern environmental monitoring, bioassays, and analytical chemistry. Thus, ZnO nanoparticles with embedded Ag nanocrystals constitute a novel class of advanced nanohybrid substrates for use in multiple applications of surface-enhanced Raman scattering metrology.
RÉSUMÉ
Thin films of Bi3+ doped LaOCl and LaOF phosphors prepared via the pulsed laser deposition (PLD) technique in vacuum and different argon (Ar) pressures were compared in order to assess their luminescence properties. All peaks of the X-ray diffraction patterns of the films were consistent with the tetragonal structure of the LaOCl and LaOF, but in the case of LaOF the signal was weaker and not all peaks were present, suggesting some preferred orientation. Photoluminescence measurements revealed that the films exhibited emission around 344 nm for LaOCl:Bi and 518 nm for LaOF:Bi under excitations of 266 nm and 263 nm, respectively. The luminescence from the LaOF:Bi sample was less intense compared to the LaOCl:Bi sample prepared under the same conditions, which was also the case for the powder samples. The amount of ablated material present on the substrate was much less for LaOF:Bi compared to LaOCl:Bi, which is attributed to the greater bandgap and hence weaker absorption of the laser pulses for LaOF:Bi. Therefore phosphors based on LaOCl as the host material were found to be preferable over LaOF under the PLD conditions used in this study.
RÉSUMÉ
Solar heat management & green air-conditioning are among the major technologies that could mitigate heat islands phenomenon while minimizing significantly the CO2 global foot-print within the building & automotive sectors. Chromogenic materials in general, and thermochromic smart coatings especially are promising candidates that consent a noteworthy dynamic solar radiation Infrared (NIR-IR) regulation and hence an efficient solar heat management especially with the expected increase of the global seasonal temperature. Within this contribution, two major challenging bottlenecks in vanadium oxide based smart coatings were addressed. It is validated for the first time that the NIR-IR modulation of the optical transmission (∆TTRANS = T(TãTMIT) - T(TãTMIT) of Vanadium oxide based smart coatings can be controlled & tuned. This upmost challenging bottle-neck controllability/tunability is confirmed via a genuine approach alongside to a simultaneous drastic reduction of the phase transition temperature TMIT from 68.8 °C to nearly room temperature. More precisely, a substantial thermochromism in multilayered V2O5/V/V2O5 stacks equivalent to that of standard pure VO2 thin films but with a far lower transition temperature, is reported. Such a multilayered V2O5/V/V2O5 thermochromic system exhibited a net control & tunability of the optical transmission modulation in the NIR-IR (∆TTRANS) via the nano-scaled thickness' control of the intermediate Vanadium layer. In addition, the control of ∆TTRANS is accompanied by a tremendous diminution of the thermochromic transition temperature from the elevated bulk value of 68.8 °C to the range of 27.5-37.5 ºC. The observed remarkable and reversible thermochromism in such multilayered nano-scaled system of V2O5/V/V2O5 is likely to be ascribed to a noteworthy interfacial diffusion, and an indirect doping by alkaline ions diffusing from the borosilicate substrate. It is hoped that the current findings would contribute in advancing thermochromic smart window technology and their applications for solar heat management in glass windows in general, skyscraper especially & in the automotive industry. If so, this would open a path to a sustainable green air-conditioning with zero-energy input.
RÉSUMÉ
Pulsed laser deposited films on glass substrate deposited at different substrate temperatures (Ts) and partial pressures of oxygen, Ho3+-doped Bi2O3 films were produced. The degradation capability of the Rhodamine B dye using the Bi2O3:Ho3+ films was explored. The impact of the Bi2O3:Ho3+ content on the dye degradation performance was analyzed. The X-ray powder diffraction patterns showed that the films deposited at 400 °C had an α-Bi2O3 phase. The impacts of various Ts and O2 partial pressures were correlated with the surface morphology and the thickness of the films using results of field emission scanning electron microscope. The thin films deposited at a low O2 partial pressure of 5-20 mTorr at Ts = 400 °C exhibited nano-needles with an average size of 80 nm and a length of â¼750 nm. The estimated band gap of the prepared films was found to vary between 2.6 and 3.0 eV. The photoluminescence (PL) of the Bi2O3:Ho3+ thin films excited at 450 nm showed an intense green band emission observed at 548 nm, and the feeble emissions at 654 and 753 nm were ascribed to the transitions of Ho3+. The nano-needle particles of the α-Bi2O3:Ho3+ exhibited a maximum PL intensity for the 20 mTorr O2 partial pressure thin film. The films prepared in vacuum and with an O2 partial pressure of 5 mTorr exhibited a 41 % dye degradation efficiency during a duration of 270 min of the photocatalysis experiment.
RÉSUMÉ
Visible and near-infrared (NIR) upconversion luminescence (UCL) emissions originating from the BaY2F8: Yb3+, Tm3+ systems were investigated under a laser excitation at 980 nm. The BaY2F8:20 mol% Yb3+, x mol% Tm3+ and BaY2F8: y mol% Yb3+, 0.5 mol% Tm3+ phosphors showed prominent UCL at 800 and 810 nm. The optimized doping concentrations of Yb3+ and Tm3+ in the BaY2F8 host matrix were evaluated, their spectroscopic properties were determined, and studies on their temperature-dependent behaviour were carried out. The temperature-sensing properties were studied by generating the fluorescence intensity ratio (FIR) of the UCL peaks originating from the thermally-coupled energy levels of the Tm3+ ions. The Stark sublevels of 1G4 level of Tm3+ ions were utilized to estimate the temperature-sensing abilities of the phosphor.
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ZnTiO3:Er3+,Yb3+ thin film phosphors were successfully deposited by pulsed laser deposition (PLD) at different substrate temperatures. The distribution of the ions in the films was investigated and the chemical analysis showed that the doping ions were homogeneously distributed in the thin films. The optical response of the phosphors revealed that the reflectance percentages of the ZnTiO3:Er3+,Yb3+ vary with the silicon substrate temperature due to the differences in the thickness and morphological roughness of the thin films. Under 980 nm diode laser excitation, the ZnTiO3:Er3+,Yb3+ film phosphors displayed up-conversion emission from the Er3+ electronic transitions, with violet, blue, green, and red emission lines at 410, 480, 525, 545 and 660 nm from 2H9/2 â 4I15/2, 4F7/2 â 4I15/2, 2H11/2 â 4I15/2, 4S3/2 â 4I15/2 and 4F9/2 â 4I15/2 transitions, respectively. The up-conversion emission was enhanced by increasing the silico (Si) substrate temperature during the deposition. Based on the photoluminescence properties and decay lifetime analysis, the energy level diagram was established and the up-conversion energy-transfer mechanism was discussed in detail.
RÉSUMÉ
Liquefied petroleum gas (LPG), which is mainly composed of hydrocarbons, such as propane and butane, is a flammable gas that is considered a clean source of energy. Currently, the overwhelming use of LPG as fuel in vehicles, domestic settings, and industry has led to several incidents and deaths globally due to leakage. As a result, the appropriate detection of LPG is vital; thus, gas-sensing devices that can monitor this gas rapidly and accurately at room temperature, are required. This work reviews the current advances in LPG gas sensors, which operate at room temperature. The influences of the synthesis methods and parameters, doping, and use of catalysts on the sensing performance are discussed. The formation of heterostructures made from semiconducting metal oxides, polymers, and graphene-based materials, which enhance the sensor selectivity and sensitivity, is also discussed. The future trends and challenges confronted in the advancement of LPG room temperature operational gas sensors, and critical ideas concerning the future evolution of LPG gas sensors, are deliberated. Additionally, the advancements in the next-generation gas sensors, such as the wireless detection of LPG leakage, self-powered sensors driven by triboelectric/piezoelectric mechanisms, and artificial intelligent systems are also reviewed. This review further focuses on the use of smartphones to circumvent the use of costly instruments and paves the way for cost-efficient and portable monitoring of LPG. Finally, the approach of utilizing the Internet of Things (IoT) to detect/monitor the leakage of LPG has also been discussed, which will provide better alerts to the users and thus minimize the effects of leakages.
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Luminescence properties of CaF2:Tb3+ nanoparticles were studied in order to investigate the effect of CaF2 native defects on the photoluminescence dynamics of Tb3+ ions. Incorporation of Tb ions into the CaF2 host was confirmed by X-ray diffraction and X-ray photoelectron spectroscopy. Cross-relaxation energy transfer was observed from the photoluminescence spectra and decay curves upon excitation at 257 nm. However, the unusual long lifetime of the Tb3+ ion as well as the decreasing trend of emission lifetime of the 5D3 level suggested the involvement of traps, which were further investigated by using temperature-dependent photoluminescence measurements, thermoluminescence and lifetime measurements at different wavelengths. This work highlights the critical role that the CaF2 native defects play in the photoluminescence dynamics of Tb3+ ions incorporated in a CaF2 matrix. The sample doped with 10 mol% of Tb3+ ions was found to be stable under prolonged 254 nm ultraviolet irradiation.
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Colloidal synthesis of CsPbBr3 nanoparticles (NPs) is often carried out by involving polar solvents that threaten the chemical stability of the NPs. Here, we report a polar-solvent-free synthesis of all-inorganic CsPbBr3 NPs by employing an ultrasonic bath approach. The phase evolution of the CsPbBr3 NPs strongly depended on the duration of ultrasonication. A secondary phase of Cs4PbBr6 was also found to evolve, which emitted narrow blue-emission bands. For the longest period of ultrasonication (12 h), the CsPbBr3 and Cs4PbBr6 phases co-existed to produce blue and green emission bands with a photoluminescence quantum yield (PLQY) of 53%. The purest form of CsPbBr3 phases was observed for the NPs produced by sonicating the precursors for 8 h. They exhibited narrow green emission bands with a PLQY of 50%. The power-conversion efficiency of a silicon solar cell was remarkably increased when coated with the CsPbBr3 NPs, thus, proving its potential to be used as a spectral downshifter for Si solar cells.
RÉSUMÉ
Plasmonic nanostructures exhibiting high optical nonlinearities are widely used in the rapidly growing modern nanotechnology of nonlinear optics including biomedical applications due to their tunable plasmonic behavior. In this work, we investigate the nonlinear optical properties of uniformly distributed Au nanoparticles (NPs) embedded in pre-synthesized sodium-zinc borate glass by the well-known ion-exchange technique for optical limiting (OL) applications. Various techniques such as optical absorption spectroscopy, x-ray photoelectron spectroscopy, Transmission Electron Microscope (TEM), Photoluminescence, Time of Flight secondary mass spectroscopy and the Z scan technique were used for the characterization of these NPs. TEM confirmed spherically shaped Au NPs with varying sizes of up to 16 nm, in agreement with optical absorption spectroscopy. Nonlinear optical (NLO) properties of these Au NPs were investigated by using an open as well as close aperture Z scan technique which exhibited enhanced optical nonlinearities. The two-photon absorption (2PA) coefficients demonstrated an increasing trend while the OL threshold values demonstrated a decreasing trend as a function of heat treatment. The improved 2PA coefficients and decreased OL threshold values endorsed the Au NPs containing glasses as contending materials for the fabrication of promising optical limiters for the protection of eyes and other sensitive instruments from laser induced damages.
RÉSUMÉ
A BaY2 F8 :Yb3+ ,Ho3+ phosphor was synthesized using a simple precipitation method. The temperature-sensing properties of BaY2 F8 :Yb3+ ,Ho3+ phosphor were investigated using the fluorescence intensity ratio (FIR) of the thermally coupled energy levels (5 F4 and 5 S2 ) of Ho3+ . Energy transitions 5 F4 â5 I8 and 5 S2 â5 I8 gave rise to emission peaks at 538 nm and 549 nm, respectively. The areas under these two emission peaks were used to calculate the FIR. Temperature-dependent upconversion luminescence was recorded in the temperature range 303-623 K using a 980 nm laser excitation source. The results suggested that the BaY2 F8 :Yb3+ , Ho3+ phosphor has the potential to be used as a non-contact optical temperature sensor.
Sujet(s)
Thermométrie , Ytterbium , Baies (géographie) , Luminescence , TempératureRÉSUMÉ
In this work, we report on the synthesis of pure and Rb doped ZnO (ZnO:Rb) nanoparticles by a simple combustion technique followed by thermal treatment in an open-air atmosphere. The prepared samples were characterized using UV-vis spectroscopy, X-ray diffraction, Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), photoluminescence, Raman spectroscopy and scanning electron microscopy. The wurtzite hexagonal phase structure of ZnO and a secondary phase of Rb2ZnO2 was observed after doping ZnO with Rb. FTIR and DSC confirmed the functional groups and the thermal stability of the ZnO samples. Field emission scanning electron microscope showed an irregular shaped agglomerated morphology for the ZnO:Rb samples. The chemical states of the undoped and Rb doped samples were identified using X-ray photoelectron spectroscopy for both pure and ZnO:Rb samples. In addition, ZnO:Rb samples exhibit good antimicrobial activities against Bacillus subtilis with a change in antibacterial behaviour as compared to pure ZnO structures indicating their multifunctional applications.
Sujet(s)
Antibactériens/pharmacologie , Bacillus subtilis/effets des médicaments et des substances chimiques , Nanostructures/composition chimique , Composés organométalliques/pharmacologie , Rubidium/pharmacologie , Oxyde de zinc/pharmacologie , Antibactériens/synthèse chimique , Antibactériens/composition chimique , Tests de sensibilité microbienne , Structure moléculaire , Composés organométalliques/synthèse chimique , Composés organométalliques/composition chimique , Taille de particule , Rubidium/composition chimique , Propriétés de surface , Température , Oxyde de zinc/synthèse chimique , Oxyde de zinc/composition chimiqueRÉSUMÉ
Y2 O3 :Tm3+ and Li+ co-doped Y2 O3 :Tm3+ nanopowders were synthesized using the solution combustion method for possible application in ultraviolet (UV) light dosimetry. X-ray diffraction revealed the crystallite sizes to be in the range 21-44 nm and 30-121 nm using the Scherrer equation and the W-H plot relationship, respectively. Field emission scanning electron microscopy confirmed that, after co-doping with 4 mol% concentration of Li+ , the particles were spherical in nature with an average size of ~30 nm. Fourier transformed infrared spectroscopy results showed bands at wavenumbers of 556, 1499, 1704, 2342, 2358, 2973, 3433, and 3610 cm-1 that corresponded to the stretching and bending vibrations of Y-O, C=O and O-H. Thermoluminescence (TL) glow peaks for Y2 O3 :Tm3+ nanophosphors observed at 399 and 590 K were attributed to oxygen defects caused using UV irradiation. These oxygen defects firstly resulted in an increased prominent peak TL intensity for up to 270 min of irradiation and then a decrease. This was attributed to the presence of oxygen defect clusters that caused a reduction in recombination centres. The Li+ co-doped sample showed peaks at 356, 430, and 583 K and its intensity sublinearly increased up to 90 min and then thereafter decreased. The TL trapping parameters were calculated using computerized glow curve deconvolution methods. The Li+ co-doped sample exhibited less fading and high trap density under the UV radiation.
Sujet(s)
Lithium/composition chimique , Nanoparticules/composition chimique , Oxydes/composition chimique , Dosimétrie par thermoluminescence , Thulium/composition chimique , Ytterbium/composition chimique , Ions/composition chimique , Taille de particule , Propriétés de surface , Rayons ultravioletsRÉSUMÉ
Development of room-temperature operating gas sensors, utilizing p-type CuO nanoplatelets for air quality monitoring with excellent response, high sensitivity and good reliability, is highly desirable. Therefore, in this work, we investigated both the influence of synthesis reaction temperature and time on the sensitivity, selectivity, and response of CuO nanoplatelets prepared through the hydrothermal synthetic method, in the presence of NaOH as base, without the support of any surfactant. The gas sensing findings revealed that the CuO nanoplatelets NO2 sensitivity and selectivity can be controlled and tuned by adjusting the synthesis reaction temperature and time, while maintaining the morphology. The CuO-based sensors revealed a remarkable response of 14.5 to 20â¯ppm NO2, with a sensitivity of 0.47â¯ppm-1 at room temperature. A decrease in sensing performance was observed at higher operating temperatures. The findings affirmed that such sensor response/sensitivity is not dependent on the specific surface area and is relatively interrelated to the adsorption sites, the average crystallite size, and low charge carrier concentration, giving rise to a more pronounced change in CuO sensor resistance. The influence of relative humidity (RH) was also investigated to have an understanding of the sensor performance in real testing conditions. Additionally, the stability analyses to four cycles of different humidity percentages and gas concentration-related repeatability conditions were carried out, and the sensor revealed a slight drifting when increasing the number of testing cycles.
RÉSUMÉ
The gas-detecting ability of nanostructured ZnO has led to significant attention being paid to the development of a unique and effective approach to its synthesis. However, its poor sensitivity, cross-sensitivity to humidity, long response/recovery times and poor selectivity hinder its practical use in environmental and health monitoring. In this context, the addition of noble metals, as dopants or catalysts to modify the ZnO surface has been examined to enhance its sensing performance. Herein, we report preparation of Pd-loaded ZnO nanoparticles via a chemical precipitation approach. Various Pd loadings were employed to produce surface-modified ZnO nanostructure sensors, and their resulting NH3 sensing capabilities both in dry and humid environments were investigated. Through a comparative gas sensing study between the pure and Pd-loaded ZnO sensors upon exposure to NH3 at an optimal operating temperature of 350 °C, the Pd-loaded ZnO sensors were found to exhibit enhanced sensor responses and fast response/recovery times. The influence of Pd loading and its successful incorporation into ZnO nanostructure was examined by X-ray diffraction, high resolution-transmission electron microscopy, and X-ray photoelectron spectroscopy. XPS studies demonstrated that in all samples, Pd existed in two chemical states, namely Pd° and Pd2+. The possible sensing mechanism related to NH3 gas is also discussed in detail.
RÉSUMÉ
Oxide materials (ZnO, TiO2) doped with noble metals were synthesized using the combustion technique. The results of the addition of Ag, Au, and Pd up to a concentration of 2 mol% on the structural, optical, morphological and antimicrobial properties was considered. X-ray diffraction experiments revealed that the crystal structure of the host materials remained unaltered despite doping with noble metals. From the scanning electron microscopy results, it was evident that the doped nanoparticles aggregated in clusters of different sizes in the host matrix. The plasmonic effect was also observed in the absorbance spectra of the different doped materials. The obtained materials have shown promising antimicrobial features. All ZnO materials exhibited a high antimicrobial activity, with very low minimum inhibitory concentration values, against the planktonic growth of all tested Gram-positive and Gram-negative bacterial strains. All doped materials exhibited very good anti-biofilm activity, the lowest minimal biofilm eradication concentration values being registered for ZnO doped with Au and Pd toward Escherichia coli and for ZnO doped with Ag against Candida albicans. These results indicate the potential that these materials have for antimicrobial applications in the fields of biomedicine and environmental protection.
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Eu/Yb co-doped NaYF4 phosphors have been synthesized by the combustion method. The Eu doping was fixed and the effect of Yb doping concentration on the structural, morphological and luminescence properties has been investigated. X-ray diffraction analysis revealed that the phosphors consisted of mixed α- and ß-phases, but the ß-phase was dominant. All elements of the host and dopants, as well as adventitious C, were detected using X-ray photoelectron spectroscopy. The surface morphology showed a microrod-like structure with sharp hexagonal edges. Energy dispersive X-ray spectroscopy spectra proved the formation of the desired materials. The photoluminescence spectra illustrated the optical emission properties of Eu3+ in the red region when excited at 394â¯nm, while, under the same excitation, Yb3+ ions gave emission at 980â¯nm. The up-conversion (UC) emission of Eu/Yb co-doped NaYF4 produced a white color at the higher concentration of Yb excited by a 980â¯nm laser, which was made possible by green emission of Er contamination (from Yb source) and blue emission of Eu2+ ions. The lifetime of the Eu3+ UC luminescence at 615â¯nm was also affected by the Yb doping concentration. The temperature sensitivity associated with the Er3+ peaks at 520 and 542â¯nm was assessed as a function of temperature and the maximum of 0.0040â¯K-1 occurred at 463â¯K.
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CdO : ZnO hexagonal particles were synthesized by a sol-gel precipitation method at different annealing temperatures. A mixed crystal phase of cubic and wurtzite structures was observed from X-ray diffraction patterns. The micrographs showed hexagonal shapes of the CdO : ZnO nanocomposites particles. The energy dispersive X-ray spectroscopy mapping images showed a uniform distribution of the Cd and Zn. The CdO : ZnO nanocomposite pallet annealed at 550 °C has an electrical resistance of 0.366 kΩ at room temperature. The nanocomposites showed an excellent sensing response against oxygen gas with a sensing response of 47% at 200 °C for the CdO : ZnO particles annealed at 550 °C. The sensor response and recovery times were found to be 43s and 45s, respectively. The sensor response was due to the sorption of oxygen ions on the surfaces of the CdO : ZnO hexagonal particles.
RÉSUMÉ
Bismuth doped ZnO (BZO) phosphors have been synthesized by the combustion method. The effect of Bi doping up to 4mol% on the structural, morphological, optical and photoluminescence (PL) properties have been investigated. X-ray diffraction analysis revealed that the BZO phosphors had the hexagonal wurtzite structure. The nanocrystallite size decreased from 75 to 38nm as the Bi concentration increased up to 3mol%, but then increased slightly for 4mol% Bi. The chemical states of the synthesized BZO phosphors were investigated using X-ray photoelectron spectroscopy and revealed the presence of both Bi3+ and Bi2+ charge states. The surface morphology showed spherical grains with some small particle agglomeration. The grain agglomeration and irregular shapes increased with increasing Bi concentration in the BZO phosphor. The absorption spectra were calculated from the reflection spectra using the Kubelka-Munk function and a blue shift in the absorption was obtained. The optical bandgap varied from 3.08 to 3.11eV for increasing Bi doping concentration. The PL spectra showed a blue emission at 410-500nm and a broad red peak at 650nm. These peaks are attributed to oxygen related defects in the ZnO host. The addition of Bi decreased the red emission and enhanced the blue emission.
RÉSUMÉ
The Ag doped ZnO (ZnO:Ag) NPs with a hexagonal wurtzite structure were synthesized by a solution combustion method. X-ray absorption near edge structure (XANES) and X-ray photoelectron spectroscopy (XPS) were used to study the defects, local electronic and atomic structures before and after Ag doping. XPS and XANES studies confirmed the deficiency of concentration of defects in ZnO after Ag doping. The photoluminescence study showed the deep level emission in the orange-red region in addition to the band to band emission. It was also found that the defect related emission of ZnO was decreased with an increasing in Ag concentration. The antibacterial behaviour of ZnO and ZnO:Ag NPs was studied against the gram positive and gram negative bacteria. The role of Ag doping and defects in the ZnO NPs were discussed for the observed antibacterial and photoluminescence behaviour.