scholarly journals Electron Dynamics in Anatase TiO2 Nanoparticles by Ultrafast Broadband Deep-Ultraviolet Spectroscopy

2019 ◽  
Vol 205 ◽  
pp. 05017
Author(s):  
Edoardo Baldini ◽  
Tania Palmieri ◽  
Enrico Pomarico ◽  
Gerald Auböck ◽  
Majed Chergui

The optical bandgap of anatase TiO2 nanoparticles is dominated by bulk absorption bands in the deep-ultraviolet due to strongly bound excitons. These spectral features can be utilized as a sensitive probe of carrier and lattice dynamics inside the TiO2 nanoparticles. Here, we implement ultrafast broadband spectroscopy tuned to the exciton resonances in order to track the electron cooling in the conduction band of bare anatase nanoparticles and monitor the electron injection dynamics from an external dye in the case of sensitized anatase nanoparticles.

Author(s):  
Celeste Yunueth Torres López ◽  
Jose de Jesus Perez Bueno ◽  
Ildefonso Zamudio Torres ◽  
Maria Luisa Mendoza López ◽  
Abel Hurtado Macias ◽  
...  

The scope of this work shows novel experimental findings on preparing anatase TiO2 nanoparticles, first anodizing titanium into an organic media for obtaining TiO2 nanotubes, and using these as a photocatalytic active electrode in treating water polluted with organic contaminants. The substrates were grit blasted to obtain mechanical fixation of the generated nanotubular TiO2 structure. This was successfully achieved without diminishment of the nanotubes order and with a self-leveling of the outer surface. A new phenomenon has been investigated consisting of the process of oxidation of the nanotubes in water after anodizing. Along this process, methyl orange added to the aqueous solution was discolored as part of the redox reaction involved. The final state of the modified layer was composed of conglomerates of almost completely crystalline TiO2 nanoparticles, around 4 nm in size, consisting of anatase. SEM and TEM images show the transition of the amorphous nanotubes (atomic disorder/nanometric order) to crystalline disordered particles (atomic order/nanometric disorder).


2019 ◽  
Vol 4 (2) ◽  
pp. 26-44
Author(s):  
Celeste Yunueth Torres López ◽  
Jose de Jesus Perez Bueno ◽  
Ildefonso Zamudio Torres ◽  
Maria Luisa Mendoza López ◽  
Abel Hurtado Macias ◽  
...  

The scope of this work shows novel experimental findings on preparing anatase TiO2 nanoparticles, first anodizing titanium into an organic media for obtaining TiO2 nanotubes, and using these as a photocatalytic active electrode in treating water polluted with organic contaminants. The substrates were grit blasted to obtain mechanical fixation of the generated nanotubular TiO2 structure. This was successfully achieved without diminishment of the nanotubes order and with a self-leveling of the outer surface. A new phenomenon has been investigated consisting of the process of oxidation of the nanotubes in water after anodizing. Along this process, methyl orange added to the aqueous solution was discolored as part of the redox reaction involved. The final state of the modified layer was composed of conglomerates of almost completely crystalline TiO2 nanoparticles, around 4 nm in size, consisting of anatase. SEM and TEM images show the transition of the amorphous nanotubes (atomic disorder/nanometric order) to crystalline disordered particles (atomic order/nanometric disorder).


CrystEngComm ◽  
2015 ◽  
Vol 17 (36) ◽  
pp. 6868-6877 ◽  
Author(s):  
Jian-Li Mi ◽  
Kirsten M. Ø. Jensen ◽  
Christoffer Tyrsted ◽  
Martin Bremholm ◽  
Bo B. Iversen

The in situ PDF method provides detailed information about the formation and growth mechanisms of TiO2 anatase nanoparticles under hydrothermal conditions.


Nature ◽  
1994 ◽  
Vol 369 (6478) ◽  
pp. 296-298 ◽  
Author(s):  
B. H. Foing ◽  
P. Ehrenfreund

2010 ◽  
Vol 10 (8) ◽  
pp. 20193-20237
Author(s):  
C. M. Chen ◽  
R. P. Cageao ◽  
L. Lawrence ◽  
J. Stutz ◽  
R. J. Salawitch ◽  
...  

Abstract. The column abundance of NO3 was measured over Table Mountain Facility, CA (34.4° N, 117.7° W) from May 2003 through September 2004, using lunar occultation near full moon with a grating spectrometer. The NO3 column retrieval was performed with the differential optical absorption spectroscopy (DOAS) technique using both the 623 and 662 nm NO3 absorption bands. Other spectral features such as Fraunhofer lines and absorption from water vapor and oxygen were removed using solar spectra obtained at different airmass factors. We observed a seasonal variation, with nocturnally averaged NO3 columns between 5–7×1013 molec cm−2 during October through March, and 5–22×1013 molec cm−2 during April through September. A subset of the data, with diurnal variability vastly different from the temporal profile obtained from one-dimensional stratospheric model calculations, clearly has boundary layer contributions; this was confirmed by simultaneous long-path DOAS measurements. However, even the NO3 columns that did follow the modeled time evolution were often much larger than modeled stratospheric partial columns constrained by realistic temperatures and ozone concentrations. This discrepancy is attributed to substantial tropospheric NO3 in the free troposphere, which may have the same time dependence as stratospheric NO3.


2018 ◽  
Vol 73 (6) ◽  
pp. 601-609 ◽  
Author(s):  
Alyssa B. Zrimsek ◽  
Sergei V. Bykov ◽  
Sanford A. Asher

We demonstrate deep ultraviolet (UV) photoacoustic spectroscopy (PAS) of trace explosives using a sensitive microphone at meter standoff distances. We directly detect 10 µg/cm2 of pentaerythritol tetranitrate (PETN), 2,4,6-trinitrotoluene (TNT), and ammonium nitrate (AN) with 1 s accumulations from a 3 m standoff distance. Large PAS signals for standoff detection are achieved by exciting into the absorption bands of the explosives with a 213 nm laser. We also investigate the impact of the deep UV photochemistry of AN on the PAS signal strength and stability. We find that production of gaseous species during photolysis of AN enhances the PAS signal strength. This deep UV photochemistry can, however, limit the PAS signal lifetimes when detecting trace quantities.


1984 ◽  
Vol 32 ◽  
Author(s):  
R. E. Riman ◽  
D. M. Haaland ◽  
C.J.M. Northrup ◽  
H. K. Bowen ◽  
A. Bleier

ABSTRACTA Sr/Ti bimetallic isopropoxide complex was synthesized by two methods. The complex served as a precursor to the production of homogeneous SrTiO3 powders via alkoxide hydrolysis. Infrared spectra were obtained for Sr(OPri)2, Ti(OPri)4, and the product of the syntheses. In addition, the IR spectra of the solutions of each of the alkoxides were followed as hydrolysis reactions proceeded. Detailed analysis of the spectral features support the existence of a 1:1 Sr/Ti bimetallic alkoxide. The new Sr/Ti compound exhibits characteristic absorption bands at (1017, 993, 972, 961 cm−1), (844, 838, 827 cm−1) and (620, 596, and 572 −1). A band at 819−1 might also be associated with the new Sr/Ti bimetallic alkoxide. The infrared spectra suggest that the isopropoxide ligands in the bimetallic alkoxide are in at least three separate local environments. This information offers insight into possible structures for the complex.


2011 ◽  
Vol 11 (3) ◽  
pp. 963-978 ◽  
Author(s):  
C. M. Chen ◽  
R. P. Cageao ◽  
L. Lawrence ◽  
J. Stutz ◽  
R. J. Salawitch ◽  
...  

Abstract. The column abundance of NO3 was measured over Table Mountain Facility, CA (34.4° N, 117.7° W) from May 2003 through September 2004, using lunar occultation near full moon with a grating spectrometer. The NO3 column retrieval was performed with the differential optical absorption spectroscopy (DOAS) technique using both the 623 and 662 nm NO3 absorption bands. Other spectral features such as Fraunhofer lines and absorption from water vapor and oxygen were removed using solar spectra obtained at different airmass factors. We observed a seasonal variation, with nocturnally averaged NO3 columns between 5−7 × 1013 molec cm−2 during October through March, and 5−22 × 1013 molec cm−2 during April through September. A subset of the data, with diurnal variability vastly different from the temporal profile obtained from one-dimensional stratospheric model calculations, clearly has boundary layer contributions; this was confirmed by simultaneous long-path DOAS measurements. However, even the NO3 columns that did follow the modeled time evolution were often much larger than modeled stratospheric partial columns constrained by realistic temperatures and ozone concentrations. This discrepancy is attributed to substantial tropospheric NO3 in the free troposphere, which may have the same time dependence as stratospheric NO3.


2021 ◽  
Author(s):  
Stephane Boubanga Tombet ◽  
Jean-Philippe Gagnon ◽  
Holger Eichstaedt ◽  
Joanne Ho

<p>The use of airborne remote sensing techniques for geological mapping offers many benefits as it allows coverage of large areas in a very efficient way.  While hyperspectral imaging from airborne/spaceborne platforms is now a well-established method applied to resolve many geological problems, it has mostly been developed only in the Visible-Near Infrared (VNIR, 0.4–1.0 mm) and Shortwave Infrared (SWIR, 1.0–2.5 mm) regions of the electromagnetic spectrum. However, the reflectance spectral features measured in the VNIR and SWIR spectral ranges are generally overtones and combination bands from fundamental absorption bands at longer wavelengths, such as in the Longwave Infrared (LWIR, 8–12 mm). The single absorption bands in the VNIR and SWIR spectral ranges are often very closely spaced so that the reflectance features measured by common spectrometers in this spectral region are typically broad and/or suffer from strong overlapping, which raises selectivity issues for mineral identification in some cases.</p><p>The inherent self-emission associated with LWIR under ambient conditions allows airborne mineral mapping in various weather (cloudy, partly cloudy or clear sky) and illumination (day or night) conditions. For this reason, LWIR often refers to the thermal infrared (TIR) spectral range. Solid targets such as minerals not only emit but also reflect TIR radiation. Since the two phenomena occur simultaneously, they end-up mixed in the radiance measured at the sensor level. The spectral features observed in a TIR spectrum of the sky and the atmosphere mostly correspond to ozone, water  vapor, carbon dioxide, methane and nitrous oxide with pretty sharp and narrow features compared with the infrared signature of solid materials such as minerals. The sharp spectral features of atmospheric gases are mixed up with broad minerals features in the collected geological mapping data, to unveil the spectral features associated with minerals from TIR measurements, the respective contributions of self-emission and reflection in the measurement must be «unmixed» and the atmospheric contributions must be compensated. This procedure refers to temperature-emissivity separation (TES). Therefore, to achieve an efficient TES and atmospheric compensation, the collection time and conditions of LWIR airborne hyperspectral data is of importance. Data of a flight mission in Southern Spain collected systematically at different times of the day (morning, mid-day and night) and in different altitudes using the Telops Hyper-Cam airborne system, a passive TIR hyperspectral sensor based on Fourier transform spectroscopy, were analyzed. TES was carried out on the hyperspectral data using<strong> two</strong> different approaches: a) Telops Reveal FLAASH IR software and b) DIMAP In-scene atmospheric compensation algorithm in order to retrieve thermodynamic temperature map and spectral emissivity data. Spectral analysis of the emissivity data with different mineral mapping methods based on commercial spectral libraries was used to compare results obtained during the different flight times and altitudes using the two post-processing methodologies. The results are discussed in the light of optimizing LWIR-based airborne operations in time and altitude to achieve best results for routine field mineral mapping applications such as in mining, soil science or archaeology, where the spatial analysis of mineral and chemical distribution is essential</p>


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