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- ItemInvestigations of long-term trends in the ionosphere with world-wide ionosonde observations(München : European Geopyhsical Union, 2014) Bremer, J.Basing on model calculations by Roble and Dickinson (1989) for an increasing content of atmospheric greenhouse gases in the Earth’s atmosphere Rishbeth (1990) predicted a lowering of the ionospheric F2- and E-regions. Later Rishbeth and Roble (1992) also predicted characteristic longterm changes of the maximum electron density values of the ionospheric E-, F1-, and F2-layers. Long-term observations at more than 100 ionosonde stations have been analyzed to test these model predictions. In the E- and F1-layers the derived experimental results agree reasonably with the model trends (lowering of h'E and increase of ƒoE and ƒoF1, in the E-layer the experimental values are however markedly stronger than the model data). In the ionospheric F2-region the variability of the trends derived at the different individual stations for hmF2 as well as ƒoF2 values is too large to estimate reasonable global mean trends. The reason of the large differences between the individual trends is not quite clear. Strong dynamical effects may play an important role in the F2-region. But also inhomogeneous data series due to technical changes as well as changes in the evaluation algorithms used during the long observation periods may influence the trend analyses.
- ItemEvolution of the charge carrier plasmon in the one-dimensional metal TTF-TCNQ as a function of temperature and momentum(Bristol : Institute of Physics Publishing, 2019) Kovbasa, N.; Graf, L.; Knupfer, M.We have investigated the charge carrier plasmon in the quasi one-dimensional metal TTF-TCNQ using electron energy-loss spectroscopy. Our data reveal a negative plasmon dispersion with a slope that is independent of temperature, which is in agreement to predictions from model calculations and previous room temperature data. A plasmon energy shift upon temperature is observed, and we discuss possible contributions to this shift. The spectral width of the plasmon is rather temperature independent, but increases clearly above a momentum value of about 0.3 Å-1.
- ItemCarrier-envelope phase-tagged imaging of the controlled electron acceleration from SiO 2 nanospheres in intense few-cycle laser fields(Bristol : IOP, 2012) Zherebtsov, S.; Süßmann, F.; Peltz, C.; Plenge, J.; Betsch, K.J.; Znakovskaya, I.; Alnaser, A.S.; Johnson, N.G.; Kübel, M.; Horn, A.; Mondes, V.; Graf, C.; Trushin, S.A.; Azzeer, A.; Vrakking, M.J.J.; Paulus, G.G.; Krausz, F.; Rühl, E.; Fennel, T.; Kling, M.F.Waveform-controlled light fields offer the possibility of manipulating ultrafast electronic processes on sub-cycle timescales. The optical lightwave control of the collective electron motion in nanostructured materials is key to the design of electronic devices operating at up to petahertz frequencies. We have studied the directional control of the electron emission from 95 nm diameter SiO 2 nanoparticles in few-cycle laser fields with a well-defined waveform. Projections of the three-dimensional (3D) electron momentum distributions were obtained via single-shot velocity-map imaging (VMI), where phase tagging allowed retrieving the laser waveform for each laser shot. The application of this technique allowed us to efficiently suppress background contributions in the data and to obtain very accurate information on the amplitude and phase of the waveform-dependent electron emission. The experimental data that are obtained for 4 fs pulses centered at 720 nm at different intensities in the range (1-4)×10 13Wcm -2 are compared to quasi-classical mean-field Monte-Carlo simulations. The model calculations identify electron backscattering from the nanoparticle surface in highly dynamical localized fields as the main process responsible for the energetic electron emission from the nanoparticles. The local field sensitivity of the electron emission observed in our studies can serve as a foundation for future research on propagation effects for larger particles and field-induced material changes at higher intensities.
- ItemNo Evidence for a Significant Impact of Heterogeneous Chemistry on Radical Concentrations in the North China Plain in Summer 2014(Columbus, Ohio : American Chemical Society, 2020) Tan, Zhaofeng; Hofzumahaus, Andreas; Lu, Keding; Brown, Steven S.; Holland, Frank; Huey, Lewis Gregory; Kiendler-Scharr, Astrid; Li, Xin; Liu, Xiaoxi; Ma, Nan; Min, Kyung-Eun; Rohrer, Franz; Shao, Min; Wahner, Andreas; Wang, Yuhang; Wiedensohler, Alfred; Wu, Yusheng; Wu, Zhijun; Zeng, Limin; Zhang, Yuanhang; Fuchs, HendrikThe oxidation of nitric oxide to nitrogen dioxide by hydroperoxy (HO2) and organic peroxy radicals (RO2) is responsible for the chemical net ozone production in the troposphere and for the regeneration of hydroxyl radicals, the most important oxidant in the atmosphere. In Summer 2014, a field campaign was conducted in the North China Plain, where increasingly severe ozone pollution has been experienced in the last years. Chemical conditions in the campaign were representative for this area. Radical and trace gas concentrations were measured, allowing for calculating the turnover rates of gas-phase radical reactions. Therefore, the importance of heterogeneous HO2 uptake on aerosol could be experimentally determined. HO2 uptake could have suppressed ozone formation at that time because of the competition with gas-phase reactions that produce ozone. The successful reduction of the aerosol load in the North China Plain in the last years could have led to a significant decrease of HO2 loss on particles, so that ozone-forming reactions could have gained importance in the last years. However, the analysis of the measured radical budget in this campaign shows that HO2 aerosol uptake did not impact radical chemistry for chemical conditions in 2014. Therefore, reduced HO2 uptake on aerosol since then is likely not the reason for the increasing number of ozone pollution events in the North China Plain, contradicting conclusions made from model calculations reported in the literature. © 2020 American Chemical Society.