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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.

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