Microspectroscopies
Raman and infrared spectroscopies are used in
the micro-sampling mode to obtain vibrational spectra in the microscopic
domain. These spectra furnish molecular or compound information and
complement the elemental composition data obtained from other microprobe
techniques.
In the laser Raman microprobe (LRM),
a continuous laser beam is micro-focussed on the sample. The photons
interact with the molecules of the sample by the phenomenon of Raman
scattering, in which the largely vibrational modes of the molecules are
detected by characteristic energy transfers to and from the photon.
The optical spectrum of the scattered photons, called the (Stokes-) Raman
spectrum, is highly diagnostic of the compound(s) present in the sample
region analyzed. The analytical sample can be a bulk solid or a
single particle of micrometer size. Both organic and inorganic
compounds can be detected and identified by their characteristic spectra.
Detection limits for most scattering molecules are typically of the order
of 1-3 wt% in a non-interfering matrix. Raman microprobe
spectroscopy can be made quantitative when analysis is carried out by
means of working curves determined from standards similar in makeup and
concentration. As a molecular microprobe, the Raman microprobe
greatly complements both the electron- and ion-beam microprobes that
furnish elemental microanalysis data. Applications of Raman
microspectroscopy include the characterization of environmental particles,
a broad range of high-technology materials (e.g., ceramic coatings and
films, superconductors, synthetic diamond), and biological/pathological
microanalysis of thin sections of tissue. Recently, the Surface and
Microanalysis Science Division has been collaborating with other divisions
in the Chemical Science and Technology Laboratory to develop luminescent
glass standards for the calibration of Raman spectral intensity.
Fourier-transform infrared (FT-IR)
microspectroscopy is a second molecular microanalysis technique that
furnishes a unique vibrational spectrum whose information content allows
the characterization and often unequivocal identification of the sample,
or microscopic sampling region, under study. Thus, in the FT-IR
microscope, an apertured sample region is typically subjected to a
transmission measurement by the collimated infrared beam which, upon
subtraction of the background spectrum, leads to the
“fingerprint” sample spectrum. For most samples, the minimum
sample size is approx. 10 micrometers for analytical quality spectra to be
obtained, and here also, successful quantitation can be obtained through
the use of standards. In cases where a transmission measurement of the
sample is not possible, such as for thin films supported by an interfering
substrate, the FT-IR microscope can be operated in the
absorption-reflection mode to yield a good IR spectrum. Extensive
infrared spectral libraries exist, typically computer-based, to permit the
rapid identification of organics and polymers. These library
reference spectra generally cover the mid-infrared range where inorganic
compounds and materials usually do not show much of an infrared spectrum.
Applications of infrared microspectroscopy include the study of polymeric
fiber samples, the elucidation of conformational structure of biomolecules,
and the spectral characterization of high explosives and that of closely
related chemical agents.
Near-Field Microspectroscopy circumvents
the diffraction limit to far-field optical microspectroscopy by scattering
the near-field components of light confined by optimal wave-guide and
antenna structures. The Division has significant efforts in developing
both vibrational spectroscopy and dielectric spectroscopy as contrast
mechanisms for near-field optical microscopes. |