Pure and doped C
60
:
Organic Conductors, Superconductors and Magnets
Laszlo Mihaly
SUNY@Stony Brook
Outline
Method: IR spectroscopy
Mix of tabletop and large scale experiments
Measuring optical transmission, reflection as the function of frequency.
Two fundamental aspects:
molecular vibrations (Example:
linear molecule
, like CO
2
or CS
2
)
free electron excitations
Materials: Fullerenes and fullerides
Fullerenes discovered in 1985 by
Curl, Kroto and Smalley
The most abundant fullerene, the C
60
molecule has icosahedral molecular symmetry, and it can modified by
endohedral and on-site doping
.
Solid C
60
forms an approximate face centered cubic
fcc
structure
The fullerene molecule forms a variety of interesting
bonded structures
Solid C
60
can be
doped with alkali and alkali earth metals
, other elements and molecules.
Modes in pure C
60
Four IR allowed
modes
Spectrum of pure C
60
single crystal looks
a bit more complex....
temperature dependence
pressure dependence
comparing the natural and C
13
enriched single crystals
Model system:
Liquid CS
2
Model calculation:
Perturbed linear molecule
Two sources of "extra" modes:
Many more modes than the four "allowed" IR active modes:
symmetery breaking
Modes extend to high frequencies:
anharmonicity
Not sensitive to C
13
, except for slight line broadening
Pressure dependence and temperature dependence suggests intramolecular coupling.
All 46 fundamental vibrational modes can be deduced.
Superconductivity in K
3
C
60
What is the magnitude of the gap?
Optical and tunneling studies.
Applications