2005 36th Meeting of the Division of Atomic, Molecular and Optical Physics
Tuesday–Saturday, May 17–21, 2005;
Lincoln, Nebraska
Session B1: Matter Optics and Atom Chips
10:30 AM–12:54 PM,
Wednesday, May 18, 2005
Burnham Yates Conference Center
Room: Ballroom I
Chair: Herman Batelaan, University of Nebraska
Abstract ID: BAPS.2005.DAMOP.B1.4
Abstract: B1.00004 : Novel methods for matter interferometry with nanosized objects
12:18 PM–12:54 PM
Preview Abstract
Abstract
Author:
Markus Arndt
(Experimentalphysik, Universit\"at Wien)
We discuss the current status and prospects for novel
experimental methods
for coherence$^{1,2}$ and decoherence$^{3}$ experiments with large
molecules. Quantum interferometry with nanosized objects is
interesting for
the exploration of the quantum-classical transition. The same
experimental
setup is also promising for metrology applications and molecular
nanolithography.
Our coherence experiments with macromolecules employ a Talbot-Lau
interferometer. We discuss some modifications to this scheme,
which are
required to extend it to particles with masses in excess of
several thousand
mass units.
In particular, the detection in all previous interference
experiments with
large clusters and molecules, was based on either laser
ionization$^{1}$
(e.g. Fullerenes) or electron impact ionization$^{2}$ (e.g.
Porphyrins
etc.). However, most ionization schemes run into efficiency
limits when the
mass and complexity of the target particle increases.
Here we present experimental results for an interference detector
which is
truly scalable, i.e. one which will even improve with increasing
particle
size and complexity. ``Mechanically magnified fluorescence
imaging'' (MMFI),
combines the high spatial resolution, which is intrinsic to
Talbot Lau
interferometry with the high detection efficiency of fluorophores
adsorbed
onto a substrate.
In the Talbot Lau setup a molecular interference pattern is
revealed by
scanning the 3$^{rd}$ grating across the molecular beam$^{1}$.
The number of
transmitted molecules is a function of the relative position
between the
mask and the molecular density pattern. Both the particle
interference
pattern and the mechanical mask structure may be far smaller than
any
optical resolution limit. After mechanical magnification by an
arbitrary
factor, in our case a factor 5000, the interference pattern can
still be
inspected in fluorescence microscopy. The fluorescent molecules are
collected on a surface which is scanned collinearly and
synchronously behind
the 3rd grating. The resulting image of the interference pattern
is by far
large enough to be easily seen by the unaided eye. High contrast
interference fringes could be recorded with dyes molecules.
$^{1}$B. Brezger et al. , Phys. Rev. Lett. \textbf{88}, 100404
(2002).
$^{2}$L. Hackerm\"{u}ller et al. Phys. Rev. Lett \textbf{91},
90408 (2003).
$^{3}$L. Hackerm\"{u}ller et al. Nature 427, 711 (2004).
To cite this abstract, use the following reference: http://meetings.aps.org/link/BAPS.2005.DAMOP.B1.4