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Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

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At least 163 records · Page 9

Temperature dependence of the ozone obsorption spectrum over the wavelength range 410 to 760 nm

The ozone, O3, absorption cross sections between 410 and 760 nm, the Chappuis band, were measured at 220, 240, 260, and 280 K relative to that at room temperature using a diode array spectrometer. The measured cross sections varied very slightly, less than 1%, with decreasing temperature between 550 and 660 nm, near the peak of the Chappuis band. At wavelengths away from the peak, the absorption cross sections decreased with decreasing temperature; e.g., about 40% at 420 nm between 298 and 220 K. These results are compared with previous measurements and the impact on atmospheric measurements are discussed.

Burkholder, James B.↗

Mixed halide bulk perovskite triplet sensitizers: Interplay between band alignment, mid-gap traps, and phonons

Photon upconversion, particularly via triplet-triplet annihilation (TTA), could prove beneficial in expanding the efficiencies and overall impacts of optoelectronic devices across a multitude of technologies. The recent development of bulk metal halide perovskites as triplet sensitizers is one potential step toward the industrialization of upconversion-enabled devices. In this work, we investigate the impact of varying additions of bromide into a lead iodide perovskite thin film on the TTA upconversion process in the annihilator molecule rubrene. We find an interplay between the bromide content and the overall device efficiency. In particular, a higher bromide content results in higher internal upconversion efficiencies, enabled by more efficient charge extraction at the interface, likely due to a more favorable band alignment. However, the external upconversion efficiency decreases, as the absorption cross section in the near infrared is reduced. The highest upconversion performance is found in our study for a bromide content of 5%. This result can be traced back to a high absorption cross section in the near infrared and higher photoluminescence quantum yield in comparison to the iodide-only perovskite, as well as an increased driving force for charge transfer.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

The measurement of O2 number density by absorption of Lyman alpha

Measurements of O2 number density obtained from rocket observations of the absorption profile of solar Lyman alpha (1216 A) have been compared with values derived from nearly simultaneous measurements of atmospheric density from other rocket techniques: grenades, falling sphere, and Pitot tube. All launches were from Wallops Island, Virginia. The atmospheric density derived from the absorption spectroscopy data is found to be about 20% less than that from the other techniques when a constant value of the absorption cross section of 1.0 times 10 to the minus 20th sq cm is used. The agreement is worse when the cross section is allowed to vary across the width of the solar line. The data in the altitude range 70-90 km are interpreted as showing that the effective value of the absorption cross section at Lyman alpha for O2 at 200 K and negligible pressure is about 0.8 times 10 to the minus 20th sq cm.

Smith, L. G.↗

Temperature dependence of the ClONO2 UV absorption spectrum

The temperature dependence of the ClONO2 absorption spectrum has been measured between 220 and 298 K and between 195 and 430 nm using a diode array spectrometer. The absorption cross sections were determined using both: (1) absolute pressure measurements at 296 K and (2) measurements at various temperatures relative to 296 K using a dual absorption cell arrangement. The temperature dependence of the ClONO2 absorption spectrum shows very broad structure. The amplitude of the temperature dependence relative to that at 296 K is weak at short wavelengths, less than 2% at 215 nm and 220 K, but significant at the wavelengths important in the stratosphere, about 30% at 325 nm and 220 K. Our ClONO2 absorption cross section data are in good general agreement with the previous measurements of Molina and Molina (1979).

Burkholder, James B.↗

Radiometric remote sensing of mesospheric and stratospheric water vapor

The remote sensing of stratospheric and mesospheric water vapor by microwave and millimeter radiometry is described. The received radiation is emitted by and interacts with all levels of the atmosphere. The pressure dependence of the linewidth for the absorption cross section of water vapor permits retrieval of vapor mixing ratios. The 183.31-GHz line of water vapor can also be used for remote sensing of the water vapor concentration in the upper atmosphere, but due to the much stronger absorption cross section for this line, ground-based observations are difficult. To date all measurements at 183 GHz have been made from platforms above the troposphere.

Croskey, Charles L.↗

Photoabsorption cross sections of OH at 115-183 nm

The absorption spectrum for OH was obtained in the 115-183 nm region. The OH radicals were produced by a pulse discharge of trace H2O in few torr of Ar. Absorption cross sections were obtained by calibration with absorption of the OH (X 2 Pi to A 2 Sigma +) transition. The features in the absorption spectrum are correlated with the excited states 1 2 Sigma -, D 2 Sigma -, 1 2 Delta, B 2 Sigma + and possibly others calculated by van Dishoeck, Langhoff, and Dalgarno. The measured cross sections are comparable with the calculated values.

Nee, J. B.↗

An experimental determination of the cross section of the Swings band system of C3

The spectral absorption cross section of the Swings band of C3 was determined from measurements behind incident shock waves that heated a gas mixture of argon and acetylene. These measurements spanned the spectral region between 300 and 540 nm, and were obtained at temperatures between 3200 and 4000 K. An electronic oscillator strength of 0.033 was deduced from the measurements.

Cooper, D. M.↗

Small scale H I structure and the soft X-ray background

The observed anticorrelation between diffuse soft X-ray flux and H I column density has been explained as absorption of soft X-rays produced in a hot galactic halo, assuming that the neutral interstellar material is sufficiently clumped to reduce the soft X-ray absorption cross section by a factor of two to three. A 21 cm emission line study of H I column density variations at intermediate and high galactic latitudes to 10' spatial resolution has been done. The results confirm conclusions from preliminary work at coarser resolution, and in combination with other data appear to rule out the hypothesis that clumping of neutral interstellar matter on any angular scale significantly reduces X-ray absorption cross sections in the 0.13 - 0.28 keV energy range. It is concluded therefore that the observed anticorrelation is not primarily a consequence of absorption of soft X-rays produced in a hot galactic halo.

Jahoda, K.↗

Small-scale H I structure and the soft X-ray background

The observed anticorrelation between diffuse soft X-ray flux and H I column density has been explained as absorption of soft X-rays produced in a hot Galactic halo, assuming that the neutral interstellar material is sufficiently clumped to reduce the soft X-ray absorption cross section by a factor of two to three. A 21-cm emission-line study of H I column density variations at intermediate and high Galactic latitudes is extended to 10 arcmin spatial resolution. The results confirm conclusions from preliminary work at coarser resolution, and, in combination with other data, appear to rule out, on any angular scale, the hypothesis that clumping of neutral interstellar matter significantly reduces X-ray absorption cross sections in the 0.13-0.28 keV energy range. It is concluded therefore that the observed anticorrelation is not primarily a consequence of absorption of soft X-rays produced in a hot Galactic halo.

Jahoda, Keith↗

The Role of Spin–Orbit Coupling in the Linear Absorption Spectrum and Intersystem Crossing Rate Coefficients of Ruthenium Polypyridyl Dyes

The successful use of molecular dyes for solar energy conversion requires efficient charge injection, which in turn requires the formation of states with sufficiently long lifetimes (e.g., triplets). The molecular structure elements that confer this property can be found empirically, however computational predictions using ab initio electronic structure methods are invaluable to identify structure-property relations for dye sensitizers. The primary challenge for simulations to elucidate the electronic and nuclear origins of these properties is a spin-orbit interaction which drives transitions between electronic states. Here, in this work, we present a computational analysis of the spin-orbit corrected linear absorption cross sections and intersystem crossing rate coefficients for a derivative set of phosphonated tris(2,2'-bipyridine)ruthenium(2+) dye molecules. After sampling the ground state vibrational distributions, the predicted linear absorption cross sections indicate that the mixture between singlet and triplet states plays a crucial role in defining the line shape of the metal-to-ligand charge transfer bands in these derivatives. Additionally, an analysis of the intersystem crossing rate coefficients suggests that transitions from the singlet into the triplet manifolds are ultrafast with rate coefficients on the order of 10 13 s -1 for each dye molecule.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Ultraviolet absorption spectrum of HOCl

The room temperature UV absorption spectrum of HOCl was measured over the wavelength range 200 to 380 nm with a diode array spectrometer. The absorption spectrum was identified from UV absorption spectra recorded following UV photolysis of equilibrium mixtures of Cl2O/H2O/HOCl. The HOCl spectrum is continuous with a maximum at 242 nm and a secondary peak at 304 nm. The measured absorption cross section at 242 nm was (2.1 +/- 0.3) x 10 exp -19/sq cm (2 sigma error limits). These results are in excellent agreement with the work of Knauth et al. (1979) but in poor agreement with the more recent measurements of Mishalanie et al. (1986) and Permien et al. (1988). An HOCl nu2 infrared band intensity of 230 +/- 35/sq cm atm was determined based on this UV absorption cross section. The present results are compared with these previous measurements and the discrepancies are discussed.

Burkholder, James B.↗

Role of small ice crystals in radiative properties of cirrus: A case study, FIRE II, November 22, 1991

Aircraft observations of cirrus cloud were made near Coffeyville, Kansas, during November 1991 as part of the First ISCCP Regional Experiment II (FIRE II) project. Cloud ice particle spectra measurements were made using both a particle measuring system (PMS) 2DC probe and an ice particle replicator. Particles larger than 200 micrometers were column rosettes. The replicator shows the presence of large numbers of ice crystals smaller than 66 micrometers (two PMS size bins) that are not recorded by the PMS 2DC probe. Calculations based on the replicator data of the geometrical blocked area and absorption cross section of the cloud per unit volume show that small particles can contribute significantly to and sometimes dominate both the solar extinction and the infrared emission. Intercomparison is made of the ice particle size, area, and mass distributions determined by these different instruments. Power law relationships for area occluded by a crystal as a function of crystal maximum dimension were computed from the PMS 2DC data. The wavelength-dependent infrared absorption cross section per volume was computed using a simple model based on anomalous diffraction and area and mass dimensional relationships for the ice crystals.

Arnott, W. Patrick↗

Study of sulfur-containing molecules in the EUV region. I - Photoabsorption cross section of SO2

Using synchrotron radiation as a continuum background, the absorption cross sections of SO2 have been measured using a double ionization chamber. The cross sections range from 10 to a maximum value of 56 Mb in the 175-760 A region. A possible window resonance series was observed and tentatively assigned to a Ryberg series converging to the (6a sub 1) to the -1st ion state. From the fluorescence excitation function the vibrational progressions of the SO2(+) ion states have been measured and found in good agreement with those observed from photoelectron spectroscopy. The same correspondence between peaks in the fragment fluorescence excitation function and the photoelectron spectrum suggests that these ion states of SO2 are dissociative in nature.

Wu, C. Y. R.↗