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We study structural and bonding changes in molecular
solids under applied pressure using optical (Raman and IR absorption)
spectroscopy in the Diamond Anvil Cell. The two techniques are complementary
in the following ways: |
FT-IR Spectroscopy
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Fourier transform infrared (FT-IR) spectroscopy measures
dominantly vibrations of functional groups and highly polar
bonds..
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FT-IR spectrometers record the interaction of IR radiation
with the sample, measuring the frequencies at which the
sample absorbs the radiation and the intensities of the
absorptions.
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Sensitive to hetero-nuclear functional group vibrations
especially OH stretch in water
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Method imposes constraints on sample thickness, uniformity
and dilution to avoid saturation.
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Requires N2 purging or vacuum to avoid strong absorption
by atmospheric water vapor.
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Good sensitivity
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More difficult to use microscopic techniques for DAC measurements
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Raman Spectroscopy
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Raman spectroscopy depends on a change in the induced
dipole moment or polarization to produce Raman scattering
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When a beam of photons strikes a molecule the photons
are scattered elastically (Rayleigh scattering) and inelastically
(Raman scattering) generating Stoke's and anti-Stokes lines.
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Sensitive to homo-nuclear molecular bonds: for example,
it can distinguish between C-C, C=C and C≡C bonds
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Useful for studying the external vibrations in condensed
molecular systems
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Requires little sample prep
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Presence of fluorescence can prohibit a spectrum being
taken, not a major problem with FT-Raman
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Fair sensitivity
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Good microscopic technique
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Optical spectroscopy measurements in the DAC reveal bonding changes
in CO2 from a molecular O=C=O to a single bonded tetrahedrally
coordinated extended solid (similar to SiO2): |
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Samples above 2000K emit a large amount of Planck
radiation. The broad thermal background generated from high temperatures
easily overwhelms any signal generated by classical Raman spectroscopy.
However, CARS (Coherent Anti-Stokes Raman Spectroscopy) provides
us with a means of generating a Raman signal that is largely spatially
and temporally isolated from this incandescent background. Thus,
we have constructed a laser system capable of providing the two
colors necessary for broadband CARS for any Raman active vibration
of interest. This has been accomplished by the construction of two
cavity dumped dye lasers which are synchronously pumped by a mode
locked Q-switched Nd:YAG laser. One of the dye lasers is set up
to be broadband, while the other is narrow band and tunable. The
two pulses (one broadband plus one narrow band from either the other
dye laser or the frequency doubled Nd:YAG) must overlap in the sample
spatially and temporally to be effective. The typical time scale
of the pulses used in our CARS experiment is ~100 ps for the frequency
doubled Nd:YAG pulses and 30 ps for the dye pulses. This means that
we have subnanosecond time resolution that can be used with a Q-switched
Nd:YAG pulse (typical duration of 100 ns) for heating. However,
it must be noted that for CARS to work a sample must be transparent
and have a significant third order polarizability. Fortunately,
diamond, hydrogen, methane and nitrogen have these properties. |
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Direct cw laser heating with either a Nd:YAG or CO2
laser is ineffective for most samples. There are no electronic or
vibronic absorption bands for most of the molecules listed above
in the region that those two lasers operate. Some molecules, such
as N2 and H2, have no dipole moment and absorb
only in the vacuum UV (which is opaque to diamond). Although they
cannot be heated directly, we can fabricate a target for laser heating
a sample indirectly. By using EDM (Electric Discharge Machining)
we have made toroids composed of tantalum or tungsten metal. These
toroids typically have an outer diameter of 90 microns and an inner
diameter of 40 microns while being only 15 microns thick. These
dimensions are slightly smaller than that of a typical sample at
20 GPa. The toroid must be placed so as not to touch either diamond
culet. By focusing the laser on the toroid, the part of the sample
inside the toroid aperture will be heated to the same temperature
as the inner toroid wall. The result is a finite sample volume of
a measurable uniform temperature. This setup allows for the laser
beams of a CARS experiment to cross inside the aperture. The toroids
can withstand temperatures well in excess of 3000K at high pressure.
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