4,495 research outputs found

    Upper limit for the D2H+ ortho-to-para ratio in the prestellar core 16293E (CHESS)

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    The H3+ ion plays a key role in the chemistry of dense interstellar gas clouds where stars and planets are forming. The low temperatures and high extinctions of such clouds make direct observations of H3+ impossible, but lead to large abundances of H2D+ and D2H+, which are very useful probes of the early stages of star and planet formation. The ground-state rotational ortho-D2H+ 111-000 transition at 1476.6 GHz in the prestellar core 16293E has been searched for with the Herschel/HIFI instrument, within the CHESS (Chemical HErschel Surveys of Star forming regions) Key Program. The line has not been detected at the 21 mK km/s level (3 sigma integrated line intensity). We used the ortho-H2D+ 110-111 transition and para-D2H+ 110-101 transition detected in this source to determine an upper limit on the ortho-to-para D2H+ ratio as well as the para-D2H+/ortho-H2D+ ratio from a non-LTE analysis. The comparison between our chemical modeling and the observations suggests that the CO depletion must be high (larger than 100), with a density between 5e5 and 1e6 cm-3. Also the upper limit on the ortho-D2H+ line is consistent with a low gas temperature (~ 11 K) with a ortho-to-para ratio of 6 to 9, i.e. 2 to 3 times higher than the value estimated from the chemical modeling, making it impossible to detect this high frequency transition with the present state of the art receivers.Comment: Accepted in A&

    Polar optical phonon scattering and negative Kromer-Esaki-Tsu differential conductivity in bulk GaN

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    Cataloged from PDF version of article.GaN is being considered as a viable alternative semiconductor for high-power solid-state electronics. This creates a demand for the characterization of the main scattering channel at high electric fields. The dominant scattering mechanism for carriers reaching high energies under the influence of very high electric fields is the polar optical phonon (POP) emission. To highlight the directional variations, we compute POP emission rates along high-symmetry directions for the zinc-blende and wurtzite crystal phases of GaN. Our treatment relies on the empirical pseudopotential energies and wave functions. The scattering rates are efficiently computed using the Lehmann-Taut Brillouin zone integration technique. For both crystal phases, we also consider the negative differential conductivity possibilities associated with the negative effective mass part of the band structure. (C) 2001 Elsevier Science B.V. All rights reserved

    Analysis of particulate emissions from tropical biomass burning using a global aerosol model and long-term surface observations

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    We use the GLOMAP global aerosol model evaluated against observations of surface particulate matter (PM₂⋅₅) and aerosol optical depth (AOD) to better understand the impacts of biomass burning on tropical aerosol over the period 2003 to 2011. Previous studies report a large underestimation of AOD over regions impacted by tropical biomass burning, scaling particulate emissions from fire by up to a factor of 6 to enable the models to simulate observed AOD. To explore the uncertainty in emissions we use three satellite-derived fire emission datasets (GFED3, GFAS1 and FINN1). In these datasets the tropics account for 66-84% of global particulate emissions from fire. With all emission datasets GLOMAP underestimates dry season PM₂⋅₅ concentrations in regions of high fire activity in South America and underestimates AOD over South America, Africa and Southeast Asia. When we assume an upper estimate of aerosol hygroscopicity, underestimation of AOD over tropical regions impacted by biomass burning is reduced relative to previous studies. Where coincident observations of surface PM₂⋅₅ and AOD are available we find a greater model underestimation of AOD than PM₂⋅₅, even when we assume an upper estimate of aerosol hygroscopicity. Increasing particulate emissions to improve simulation of AOD can therefore lead to overestimation of surface PM₂⋅₅ concentrations. We find that scaling FINN1 emissions by a factor of 1.5 prevents underestimation of AOD and surface PM₂⋅₅ in most tropical locations except Africa. GFAS1 requires emission scaling factor of 3.4 in most locations with the exception of equatorial Asia where a scaling factor of 1.5 is adequate. Scaling GFED3 emissions by a factor of 1.5 is sufficient in active deforestation regions of South America and equatorial Asia, but a larger scaling factor is required elsewhere. The model with GFED3 emissions poorly simulates observed seasonal variability in surface PM₂⋅₅ and AOD in regions where small fires dominate, providing independent evidence that GFED3 underestimates particulate emissions from small fires. Seasonal variability in both PM₂⋅₅ and AOD is better simulated by the model using FINN1 emissions. Detailed observations of aerosol properties over biomass burning regions are required to better constrain particulate emissions from fires

    Comparative analysis of zinc-blende and wurtzite GaN for full-band polar optical phonon scattering and negative differential conductivity

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    Cataloged from PDF version of article.For high-power electronics applications, GaN is a promising semiconductor. Under high electric fields, electrons can reach very high energies where polar optical phonon (POP) emission is the dominant scattering mechanism. So, we undertake a full-band analysis of POP scattering of conduction-band electrons based on an empirical pseudopotential band structure. To uncover the directional variations, we compute POP emission rates along high-symmetry directions for the zinc-blende (ZB) crystal phase of GaN. We also compare the results with those of the wurtzite phase. In general, the POP scattering rates in the zinc-blende phase are lower than the wurtzite phase. Our analysis also reveals appreciable directional dependence, with the Gamma-L direction of ZB GaN being least vulnerable to POP scattering, characterized by a scattering time of 11 fs. For both crystal phases, we consider the negative differential conductivity possibilities driven by the negative effective mass part of the band structure. According to our estimation, for the ZB phase the onset of this effect requires fields above similar to 1 MV/cm. (C) 2000 American Institute of Physics. [S0003-6951(00)02743-1]

    Suppression of electron relaxation and dephasing rates in quantum dots caused by external magnetic fields

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    An external magnetic field has been applied in laterally coupled dots (QDs) and we have studied the QD properties related to charge decoherence. The significance of the applied magnetic field to the suppression of electron-phonon relaxation and dephasing rates has been explored. The coupled QDs have been studied by varing the magnetic field and the interdot distance as other system parameters. Our numerical results show that the electron scattering rates are strongly dependent on the applied external magnetic field and the details of the double QD configuration.Comment: 13 pages, 6 figure

    Screening effects in the electron-optical phonon interaction

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    We show that recently reported unusual hardening of optical phonons renormalized by the electron-phonon interaction is due to the neglect of screening effects. When the electron-ion interaction is properly screened optical phonons soften in three dimension. It is important that for short-wavelength optical phonons screening is static while for long-wavelength optical phonons screening is dynamic. In two-dimensional and one-dimensional cases due to crossing of the nonperturbed optical mode with gapless plasmons the spectrum of renormalized optical phonon-plasmon mode shows split momentum dependence.Comment: 7 page

    Photochemistry in the arctic free troposphere: NOx budget and the role of odd nitrogen reservoir recycling

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    The budget of nitrogen oxides (NOx) in the arctic free troposphere is calculated with a constrained photochemical box model using aircraft observations from the Tropospheric O3 Production about the Spring Equinox (TOPSE) campaign between February and May. Peroxyacetic nitric anhydride (PAN) was observed to be the dominant odd nitrogen species (NOy) in the arctic free troposphere and showed a pronounced seasonal increase in mixing ratio. When constrained to observed acetaldehyde (CH3CHO) mixing ratios, the box model calculates unrealistically large net NOx losses due to PAN formation (62pptv/day for May, 1-3km). Thus, given our current understanding of atmospheric chemistry, these results cast doubt on the robustness of the CH3CHO observations during TOPSE. When CH3CHO was calculated to steady state in the box model, the net NOx loss to PAN was of comparable magnitude to the net NOx loss to HNO3 (NO2 reaction with OH) for spring conditions. During the winter, net NOx loss due to N2O5 hydrolysis dominates other NOx loss processes and is near saturation with respect to further increases in aerosol surface area concentration. NOx loss due to N2O5 hydrolysis is sensitive to latitude and month due to changes in diurnal photolysis (sharp day-night transitions in winter to continuous sun in spring for the arctic). Near NOx sources, HNO4 is a net sink for NOx; however, for more aged air masses HNO4 is a net source for NOx, largely countering the NOx loss to PAN, N2O5 and HNO3. Overall, HNO4 chemistry impacts the timing of NOx decay and O3 production; however, the cumulative impact on O3 and NOx mixing ratios after a 20-day trajectory is minimal. © 2003 Elsevier Science Ltd. All rights reserved

    Photochemistry in the arctic free troposphere: Ozone budget and its dependence on nitrogen oxides and the production rate of free radicals

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    Abstract. Local ozone production and loss rates for the arctic free troposphere (58–85 ◩ N, 1–6 km, February–May) during the Tropospheric Ozone Production about the Spring Equinox (TOPSE) campaign were calculated using a constrained photochemical box model. Estimates were made to assess the importance of local photochemical ozone production relative to transport in accounting for the springtime maximum in arctic free tropospheric ozone. Ozone production and loss rates from our diel steady-state box model constrained by median observations were first compared to two point box models, one run to instantaneous steady-state and the other run to diel steady-state. A consistent picture of local ozone photochemistry was derived by all three box models suggesting that differences between the approaches were not critical. Our model-derived ozone production rates increased by a factor of 28 in the 1–3 km layer and a factor of 7 in the 3–6 km layer between February and May. The arctic ozone budget required net import of ozone into the arctic free troposphere throughout the campaign; however, the transport term exceeded the photochemical production only in the lower free troposphere (1–3 km) between February and March. Gross ozone production rates were calculated to increase linearly with NOx mixing ratios up to ∌300 pptv in February and for NOx mixing ratio

    An empirical model of the ionospheric electric potential

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    Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/95360/1/grl12685.pd
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