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排序方式: 共有57条查询结果,搜索用时 31 毫秒
1.
Pascher W. Den Besten J. H. Caprioli D. Leijtens X. Smit M. van Dijk R. 《Optical and Quantum Electronics》2003,35(4-5):453-464
Based on a rigorous vectorial analysis, a fast travelling-wave Mach–Zehnder modulator is modelled and designed. The cross-section of the semiconductor layer stack and the lossy electrodes are carefully modelled using the method of lines in order to investigate propagation characteristics, velocity and losses. This yields an accurate microwave and optical field distribution to explain the behaviour of the component. In order to enhance the modulation efficiency, design curves are derived and the cross-sectional dimensions for minimum microwave loss are determined. The loss of the optimized modulator agrees very well with small-signal measurements up to 40 GHz and HFSS simulations. The layerstack of the fabricated device is suitable for integration with InP multi-wavelength lasers. 相似文献
2.
Jakob Heller Tobias F. Pascher Dr. Christian van der Linde Dr. Milan Ončák Prof. Dr. Martin K. Beyer 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(66):16367-16376
Hydrated aluminium cations have been investigated as a photochemical model system with up to ten water molecules by UV action spectroscopy in a Fourier transform ion cyclotron resonance (FT-ICR) mass spectrometer. Intense photodissociation was observed starting at 4.5 eV for two to eight water molecules with loss of atomic hydrogen, molecular hydrogen and water molecules. Quantum chemical calculations for n=2 reveal that solvation shifts the intense 3s–3p excitations of Al+ into the investigated photon energy range below 5.5 eV. During the photochemical relaxation, internal conversion from S1 to T2 takes place, and photochemical hydrogen formation starts on the T2 surface, which passes through a conical intersection, changing to T1. On this triplet surface, the electron that was excited to the Al 3p orbital is transferred to a coordinated water molecule, which dissociates into a hydroxide ion and a hydrogen atom. If the system remains in the triplet state, this hydrogen radical is lost directly. If the system returns to singlet multiplicity, the reaction may be reversed, with recombination with the hydroxide moiety and electron transfer back to aluminium, resulting in water evaporation. Alternatively, the hydrogen radical can attack the intact water molecule, forming molecular hydrogen and aluminium dihydroxide. Photodissociation is observed for up to n=8. Clusters with n=9 or 10 occur exclusively as HAlOH+(H2O)n-1 and are transparent in the investigated energy range. For n=4–8, a mixture of Al+(H2O)n and HAlOH+(H2O)n-1 is present in the experiment. 相似文献
3.
Erik Barwa Tobias F. Pascher Milan On
k Christian van der Linde Martin K. Beyer 《Angewandte Chemie (International ed. in English)》2020,59(19):7467-7471
We investigate activation of carbon dioxide by singly charged hydrated magnesium cations Mg .+(H2O)n, through infrared multiple photon dissociation (IRMPD) spectroscopy combined with quantum chemical calculations. The spectra of [MgCO2(H2O)n].+ in the 1250–4000 cm?1 region show a sharp transition from n=2 to n=3 for the position of the CO2 antisymmetric stretching mode. This is evidence for the activation of CO2 via charge transfer from Mg .+ to CO2 for n≥3, while smaller clusters feature linear CO2 coordinated end‐on to the metal center. Starting with n=5, we see a further conformational change, with CO2.? coordination to Mg2+ gradually shifting from bidentate to monodentate, consistent with preferential hexa‐coordination of Mg2+. Our results reveal in detail how hydration promotes CO2 activation by charge transfer at metal centers. 相似文献
4.
Optical four-wave mixing due to the resonant spin nonlinearity in n-InSb was observed in magnetic fields up to 1.4 T. The mixing of two CO-laser frequencies ω1 and ω2 = ω1 - Δω yields radiation with frequencies ω1 + 2Δω, ω1 + Δω, ω1 - 2Δω, and ω1 - 3Δω. We found the resonant contribution to the third order nonlinear susceptibility arising from the spin-flip interaction to increase by more than two orders of magnitude when ω1 is varied from 1760 cm-1 to 1896 cm-1. With the lasers working simultaneously Q-switched we observed radiation at ω1 + Δω and ω1 - 2Δω due to the mixing caused by the nonparabolicity of the conduction electrons even without an external magnetic field. At the resonant magnetic field the intensity of the mixed radiation is increased by more than one order of magnitude and is also observed when the laser pulses do not hit the sample simultaneously as long as the time difference between the two pulses does not exceed 450 ns. This points to a spin dephasing time T2 of about 100 ns. 相似文献
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7.
H. J. Höfling H. Pascher H. G. Häfele 《Applied Physics A: Materials Science & Processing》1983,31(4):195-199
We report on measurements of spin-flip Raman gain inn-Hg1?x Cd x Te (x=0.23, carrier density 1.0×1015cm?3) as a function of the magnetic field up to 1.6T. The measurements were carried out by a small signal gain technique at a temperature of 1.8 K. Furthermore, the measurements yield lineshapes and linewidths of the spontaneous scattering and allow a precise determination of the effectiveg-value. The highest gain observed is 0.2 cm/W. The band edge value of the effectiveg-value is ?93.2 and the widths of the symmetric lines are between 18 and 120 G, depending on the magnetic field. 相似文献
8.
Applying optimal control to photoinduced trans-cis isomerization in condensed phase, the dynamics of bond-twisting motion of 1,1'-diethyl-4,4'-cyanine in methanol and propanol is revealed. The shape of the optimized pulse resulting from minimization of the photoisomer formation can be directly related to the initial excited-state dynamics in close proximity to the Franck-Condon point. The solvent viscosity-dependent ultrafast wavepacket motion is reflected in the prominent down-chirp of the optimized pulses and reveals a detailed picture of the control mechanism: The reduction of the isomer production is achieved by most efficient dumping of excited population back to the trans ground state. In the higher-viscosity solvent, propanol, wavelength-dependent oscillatory features are superimposed to the overall chirp structure pointing to the importance of excited-state vibrational coherences for the dumping process. 相似文献
9.
Dietzek B Brüggemann B Pascher T Yartsev A 《Journal of the American Chemical Society》2007,129(43):13014-13021
Using optimal control as a spectroscopic tool we decipher the details of the molecular dynamics of the essential multidimensional excited-state photoisomerization - a fundamental chemical reaction of key importance in biology. Two distinct nuclear motions are identified in addition to the overall bond-twisting motion: Initially, the reaction is dominated by motion perpendicular to the torsion coordinate. At later times, a second optically active vibration drives the system along the reaction path to the bottom of the excited-state potential. The time scales of the wavepacket motion on a different part of the excited-state potential are detailed by pump-shaped dump optimal control. This technique offers new means to control a chemical reaction far from the Franck-Condon point of absorption and to map details of excited-state reaction pathways revealing unique insights into the underlying reaction mechanism. 相似文献
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