

Laser-Induced
Breakdown Spectroscopy (LIBS) is an
extremely powerful and
flexible elemental analysis technique that utilizes the energy in a
short, intense laser pulse to vaporize or “ablate” a small volume of
sample material. The ablated target material (whether solid,
liquid, or gas) absorbs enough energy to vaporize and then ionize the
constituent atoms, creating a small cloud of plasma (free ions and
electrons) that expands rapidly. As the cloud expands and cools,
a significant fraction of the ions recombine to form excited atoms,
which eventually decay via spontaneous emission to the atomic ground
state (the state of lowest energy in the atom). The photons given
off during spontaneous emission can be collected and spectrally
analyzed which provides a “spectral fingerprint” of all the constituent
elements of the target and the plasma. Since each element has a
unique spectral fingerprint, relative and absolute elemental
concentrations within the target material can be determined.
Theoretically, this measurement can be accomplished with one laser
pulse (about 10 ns), resulting in a very rapid analysis of the target
(total measurement time less than one second). Because the target
material is interrogated by a laser beam and the plasma is analyzed by
“all–optical” techniques, the analysis can be performed remotely or on
hazardous materials.

1)
LIBS as a tool to detect and identify
bacteria. The BIOMAS
Project: Bacterial Identification by Optical, Molecular, and Atomic
Spectroscopy. (Prof. Rehse/Jonathan Diedrich
/Narmatha Jeyasingham/Qassem Mohaidat/Khozima Hamasha).
In just the
last three years, it has been determined that LIBS can be utilized to
discriminate between bacterial strains on the basis of the atomic
spectrum alone. This summer will see initial investigations into
the ability to discriminate between two very common non-pathogenic
bacteria strains: Escherichia coli
and Pseudomonas aeruginosa.
Eventually, we wish to apply the technique as a clinical diagnostic
tool for the identification of such dangerous pathogens as Vibrio
cholerae (which causes cholera) and EHEC which causes kidney
damage in
children.

4)
LIBS will be used to determine the
relative concentrations of Fe in magnetic nanoparticle samples (Emmett
Brown). Iron oxide nanoparticles are prepared in a
bio-compatible alginate matrix by another research group in our
department (Lawes). This bio-compatible matrix can be introduced
into the human body and it is hoped that the magnetic nanoparticles
will provide unique behavior of medicinal value. These samples
are prepared in a chemical process, with the percent concentration of
iron being completely unknown. It is our intention to use LIBS to
measure the fractional percentage of iron in these samples, yielding a
quick and inexpensive assay of the material.
5) We are
testing the ability of LIBS to
detect trace concentrations of aluminum in a simulated tissue matrix
(Marian Adamson). This project has relevance to the
Wayne
State University Smart Sensors and Integrated Microsystems neurological
implant program. It is believed that aluminum atoms can diffuse
out of a sapphire matrix into human tissue in which an
integrated-circuit implant has been placed. This diffusion of
aluminum out of what is supposed to be an "inert" substrate is bad for
the subject and the implant. We are trying to determine whether
LIBS can be used as a sensitive probe to detect this process.
Initial investigations will begin by identifying suitable tissue
"simulants" which can be used to safely test the technique. We
will then try to determine what the limit of detection (LOD) is for Al
in such systems. Lastly, we will explore the delivery of the
laser and collection of the light via a single optical fiber to
simulate actual in vivo use of the technique.
6) Molecular
evolution in laser-created
plasmas at the air/water interface (Arathi Padmanabhan).
We are currently studying the temporal evolution and power dependence
of various molecular species in our LIBS plasmas created by ablating
the surface of water. The molecules, which result from
combination of liberated atoms in the plasma, emit detectable light to
well after 40 microseconds after the laser pulse - whereas the emission
from atomic species is gone after nearly 5 microseconds. We are
also investigating the effect of using different "bath gases" on this
behavior by performing our ablation in argon, nitrogen, and helium.
Recent Research Papers
20. E. Surdutovich, G. Setzler, W.E. Kauppila, S.J. Rehse, and T.S. Stein, “Measurements of total cross sections for positron scattering by uracil molecules,” Phys. Rev. A 77, 054701 (2008).
8. Laser Collimation of an Atomic Gallium Beam, S.J. Rehse, K.M. Bockel, and S.A. Lee, Phys. Rev. A 69, 063404 (2004)
7. Steven J. Rehse, Light Force Manipulation of Gallium Atoms, Dissertation (Ph.D.), Colorado State University, 2002
6. Generation of 125 mW Frequency Stabilized Continuous-wave Tunable Laser Light at 295 nm by Frequency Doubling in a BBO Crystal, S.J. Rehse and S.A. Lee, Opt. Comm. 213, 347 (2002)
5. Light force manipulation of an atomic gallium beam, S.J. Rehse, K. Bockel, and S.A. Lee, in Technical Digest. Summaries of papers presented at the Quantum Electronics and Laser Science Conference, 218, (IEEE 2001)
4. Measurement of the Hyperfine Structure of the 4d2D3/2,5/2 Levels and Isotope Shifts of the 4p2P3/2 - 4d2D3/2 and 4p2P3/2 - 4d2D5/2 Transitions in Gallium 69 and 71, S.J. Rehse, W.M. Fairbank Jr., and S.A. Lee, JOSA B 18, 1 (2001)
3. Optical Manipulation of Group III Atoms, S.J. Rehse, R.W. McGowan and S.A. Lee, Appl. Phys. B 70, 657 (2000)
2. Light force manipulation of group III atoms, S.J. Rehse and S.A. Lee, in Laser Spectroscopy. 14th International Conference. ICOLS99, 316, 1999
1. Nanolithography
With Metastable Neon Atoms: Enhanced Rate of Contamination Resist
Formation for Nanostructure Fabrication, S.J. Rehse, A. D. Glueck, S.A.
Lee, A.B. Goulakov, C.S. Menoni, D.C. Ralph, K.S. Johnson and M.
Prentiss, Appl. Phys. Lett. 71, 1427, (1997)
Last updated on
12/02/08