aktualisiertes pdf - DPG-Tagungen
aktualisiertes pdf - DPG-Tagungen
aktualisiertes pdf - DPG-Tagungen
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Fachsitzungen<br />
– Fach-, Kurzvorträge und Posterbeiträge –<br />
MO 1 Experimentelle Techniken<br />
Zeit: Montag 11:00–11:30 Raum: HS 332<br />
Fachvortrag MO 1.1 Mo 11:00 HS 332<br />
Autler-Townes effect as a probe of properties of excited<br />
molecular states. — •R. Garcia Fernandez 1 , A. Ekers 1 , J.<br />
Klavins 2 , L.P. Yatsenko 3 , N.N. Bezuglov 4 , O. Kaufmann 1 ,<br />
B.W. Shore 1 , and K. Bergmann 1 — 1 FB Physik, TU Kaiserslautern.<br />
— 2 Dept. of Physics, University of Latvia, Riga. — 3 Inst. of Physics of<br />
the Academy of Sciences, Kiev, Ukraine. — 4 V.A. Fock Inst. of Physics,<br />
Univ. St.Petersburg, Russia<br />
A novel method for the characterization of highly excited molecular<br />
states utilizing the Autler-Townes splitting is demonstrated for Na2<br />
molecule. The experiment employs a supersonic beam and a cascade<br />
scheme X1Σ + g → A1Σ + u → 51Σ + g (or 61Σ + g ), with a cw probe laser in<br />
the first step and a cw dressing laser in the second step. The variation of<br />
the fluorescence intensities from the intermediate and upper levels with<br />
the frequency of the pump and probe lasers contains information about<br />
the lifetime and branching ratio of the upper state. These quantities can<br />
be easily accessed by a proper choice of the detuning of pump laser from<br />
the resonance and the intensity of the probe laser. The lifetime of the<br />
51Σ + g state is measured to be about the same as that of the intermediate<br />
A 1 Σ + u state, while for 61 Σ + g it is twice as large. The 51 Σ + g<br />
state decays<br />
almost exclusively to the A 1 Σ + u state, but decay of the 6 1 Σ + u occurs predominantly<br />
through other channels.<br />
MO 2 Experimentelle Techniken, Kalte Moleküle<br />
Zeit: Montag 11:30–12:45 Raum: HS 332<br />
MO 2.1 Mo 11:30 HS 332<br />
Laser Spectroscopy of Ultracold Molecular Hydrogen Ions<br />
in a Linear RF-Trap — •Ulf Fröhlich 1 , Bernhard Roth 1 ,<br />
Thomas Fritsch 1 , Claus Lämmerzahl 2 , and Stephan Schiller 1<br />
— 1 Heinrich-Heine-Universität Düsseldorf, D-40225 Düsseldorf —<br />
2 Universität Bremen, D-28359 Bremen<br />
We present an experiment aimed at high-resolution spectroscopy of the<br />
ro-vibrational level structure of HD + . As one of the simplest molecules,<br />
HD + is particularly suitable to test theories of molecular structure.<br />
The HD + molecular ions will be confined in a linear rf-trap and cooled<br />
via Coulomb interaction by laser cooled Be + atomic ions confined in the<br />
same trap (sympathetic cooling). At sufficient high cooling rates, the<br />
laser cooled Be + ions undergo a phase transition to an ordered structure<br />
(Coulomb crystal). Numerical simulations show, that one can expect the<br />
HD + ions to be embedded in such a Be + ionic crystal. In this way, an<br />
ultra-cold ensemble of HD + molecular ions can be prepared for highresolution<br />
laser spectroscopy.<br />
So far, we have prepared and characterized Be + ionic crystals of different<br />
size and shape suitable for embedding HD + ions. Currently we are<br />
trying to optimize the process of loading HD + and Be + ions into the<br />
trap. Furthermore, we are now building up a stabilized laser system for<br />
high-resolution spectroscopy of the (ν = 0, N = 4) - (ν = 4, N = 4)<br />
transition of HD + at 1.4µm.<br />
MO 2.2 Mo 11:45 HS 332<br />
COOL MOLECULAR MICRO-BEAMS, FRIGID CLUSTERS,<br />
AND GELID MOLECULAR DIFFRACTION IMAGES —<br />
•Bretislav Friedrich — Fritz-Haber-Institut der MPG, Faradayweg<br />
4-6, D-14195 Berlin<br />
I will describe a versatile molecular beam source, employing supersonic<br />
flow, pulsing, and ablation in a way that minimizes size and pumping requirements.<br />
The performance of the source is exemplified by producing a<br />
cool pulsed supersonic molecular beam of CaF radicals, essentially without<br />
recourse to pumping. About 10 12 CaF molecules cooled to a terminal<br />
temperature of about 140 K are obtained per ablation pulse.<br />
We have developed a general technique for orienting molecules,<br />
amenable to a wide variety of species and applications. The key aspect<br />
is to endow a polar molecule with a pseudo-first-order Stark effect. I will<br />
describe how this effect comes about and discuss its use in the detection<br />
of gas-phase HXeI clusters, generated by the photolysis of HI embedded<br />
in the outer shells of large Xen clusters.<br />
I will also describe a versatile imaging detector for neutral atoms and<br />
molecules based on reactions with a vacuum-deposited silver surface. The<br />
detector is endowed with the Fellgett advantage, has a demonstrated<br />
sensitivity of several monolayers of molecules, and a dynamic range of<br />
at least 100:1. One of the immediate applications of the detector in our<br />
47<br />
cold-molecule effort will be to determining the velocity distributions of<br />
slow/cold molecules. These are convoluted in a diffraction pattern and<br />
can be extracted with a high accuracy from an observed diffraction image.<br />
MO 2.3 Mo 12:00 HS 332<br />
Anwendung kalter, langsamer Moleküle zur hochauflösenden<br />
Spektroskopie: Die Hyperfeinstruktur von 15 ND3. — Jacqueline<br />
van Veldhoven 1 , •Jochen Küpper 2 , Boris Sartakov 3 , Hendrick<br />
L. Bethlem 1 und Gerard Meijer 2 — 1 FOM Instituut voor Plasmafysica<br />
“Rijnhuizen”, Nieuwegein, Die Niederlande — 2 Fritz-Haber-Institut<br />
der MPG, Abt. Molekülphysik, Berlin — 3 Russian Academy of Science,<br />
Inst. Gen. Phys., Moskau 119991, Rußland<br />
Ultimativ ist die Auflösung jedes spektroskopischen Experiments durch<br />
die Interaktionszeit zwischen untersuchtem Objekt und Messgerät limitiert.<br />
In den letzten Jahren sind verschiedene Methoden zur Erzeugung<br />
kalter, langsamer Moleküle entwickelt worden. In unserer Gruppe erzeugen<br />
wir aus einem Überschallstrahl mit Hilfe geschalteter elektrischer<br />
Felder Bündel langsamer und kalter Moleküle [1]. In dieser Arbeit haben<br />
wir 15 ND3 im |11〉-Zustand auf 50 m/s abgebremst und an den langsamen<br />
Molekülen Mikrowellen-UV Doppelresonanzspektroskopie durchgeführt.<br />
Wir präsentieren Ergebnisse zum Inversionstunnelübergang von 15 ND3<br />
bei 1, 59 GHz mit einer Linienbreite von etwa 1 kHz. Die gegenüber den<br />
bisher höchstauflösenden Messungen [2] deutlich verringerte Linienbreite<br />
ermöglicht es einzelne Hyperfeinübergänge aufzulösen und die Hyperfeinstruktur<br />
von 15 ND3 präzise auszuwerten.<br />
[1] H.L. Bethlem und G. Meijer, Int. Rev. Phys. Chem. 22, 73 (2003)<br />
[2] J. van Veldhoven, R.T. Jongma, B. Sartakov, W.A. Bongers, und G.<br />
Meijer, Phys. Rev. A 66, 032501 (2002).<br />
MO 2.4 Mo 12:15 HS 332<br />
Generation of cold atoms and molecules by a rotating nozzle:<br />
recent progress — •D.H. Meyer, N.-N. Liu, and H.J. Loesch —<br />
Fakultaet fuer Physik, Universitaet Bielefeld, Universitaetsstrasse 25, D-<br />
33615 Bielefeld<br />
The rotating nozzle is an universal mechanical device to create a (quasi)<br />
continuous beam of cold atoms and molecules. To date we have achieved<br />
a Xe-beam featuring a most probable velocity of 40 m/s at a parallel<br />
translational temperature of T(par) =10.4 K and 20 at 20 m/s. Similar<br />
results have been obtained also for Kr. Modifications of the apparatus<br />
are being realized presently with the aim to lower the peak velocity further<br />
and to exploit the cold atoms as carrier gases for polar molecules.<br />
We will report on the results of these activities and on first experiments<br />
about the manipulation of the cold molecules by inhomogeneous electric<br />
fields. The applicability of the rotating nozzle for the continuous storage<br />
of molecules in a ring trap will be discussed.