Confinement of electrons and ions in a combined trap with the potential for antihydrogen production

Experiments with electrons and ions in a combined trap are reported. The unique capability to confine particles with opposite charge and very different mass simultaneously in the same spatial region makes the combined trap a promising device for future synthesis of antihydrogen.     

Femtosecond dynamics of secondary radiation formation from quantum well excitons

The time-resolved secondary emission of resonantly created excitons in GaAs quantum wells is studied using femtosecond up-conversion spectroscopy. The behaviour of the rise and decay of the secondary emission and reflectivity in quantum wells is strongly dependent upon the disorder at the interfaces, the exciton density and the temperature. In the case of low densities and temperatures the emission is independent of the exciton density and rises quadratically in time, in excellent agreement with recent theory for Rayleigh scattering from two-dimensional excitons subjected to disorder. These rise times are compared directly with times measured by time-integrated four-wave mixing (FWM). The comparison of the dynamics displayed in time-resolved secondary radiation and time-integrated FWM provide a clear understanding of the coherence properties of QW excitons in the first few picoseconds after excitation. High-contrast oscillations that are due to quantum beats between the heavy- and light-hole 1s-states are seen. The visibility decay at very low densities is long ps and is related to the action of potential fluctuations on the scattering of heavy-hole and light-hole excitons.     

Accurate determination of wavenumbers for iodine molecular lines in the red spectral region

The hyperfine structure of various absorption lines of molecular iodine with wavenumbers between 12980 and 13890 cm^–1 has been resolved using Doppler-free polarization spectroscopy. The wavenumbers of theo-component of 17 rovibrational lines of I₂ due to the transitionB ³ _ou ⁺ –X¹ _g ⁺ with even rotational quantum numbers have been determined with an accuracy of 0.001 cm^–1. A comparison of the centers of gravity of these 17 lines with the values of the iodine atlas of Gerstenkorn et al. yields a difference of thus corroborating the data of the iodine atlas in the red region within limits of error.     

Binding of single nucleotides to H+-ATP synthases observed by fluorescence resonance energy transfer

F(0)F(1)-ATP synthases couple proton translocation with the synthesis of ATP from ADP and phosphate. The enzyme has three catalytic nucleotide binding sites, one on each beta-subunit; three non-catalytic binding sites are located mainly on each alpha-subunit. In order to observe substrate binding to the enzyme, the H(+)-ATP synthase from Escherichia coli was labelled selectively with the fluorescence donor tetramethylrhodamine (TMR) at position T106C of the gamma-subunit. The labelled enzymes were incorporated into liposomes and catalysed proton-driven ATP synthesis. The substrate ATP-Alexa Fluor 647 was used as the fluorescence acceptor to perform intermolecular fluorescence resonance energy transfer (FRET). Single molecules are detected with a confocal set-up. When one ATP-Alexa Fluor 647 binds to the enzyme, FRET can be observed. Five stable states with different intermolecular FRET efficiencies were distinguished for enzyme-bound ATP-Alexa Fluor 647 indicating binding to different binding sites. Consecutive hydrolysis of excess ATP resulted in stepwise changes of the FRET efficiency. Thereby, gamma-subunit movement during catalysis was directly monitored with respect to the binding site with bound ATP-Alexa Fluor 647.     

Zur Bestimmung von Submikromengen von Kohlenstoff in organischen Verbindungen

Analytical and Bioanalytical Chemistry -