Erik D. Emmons

Bio: Erik D. Emmons is an academic researcher from Edgewood Chemical Biological Center. The author has contributed to research in topics: Photoionization & Raman spectroscopy. The author has an hindex of 23, co-authored 57 publications receiving 1193 citations. Previous affiliations of Erik D. Emmons include Science Applications International Corporation & Business International Corporation.

Photoexcitation of a volume plasmon in C60 ions.

Abstract: Neutral C60 is well known to exhibit a giant resonance in its photon absorption spectrum near 20 eV. This is associated with a surface plasmon, where delocalized electrons oscillate as a whole relative to the ionic cage. Absolute photoionization cross-section measurements for C+60, C2+60, and C3+60 ions in the 17-75 eV energy range show an additional resonance near 40 eV. Time-dependent density functional calculations confirm the collective nature of this feature, which is characterized as a dipole-excited volume plasmon made possible by the special fullerene geometry.

Photoexcitation of a Volume Plasmon in C$_{60}$ Ions

Abstract: Neutral C60 is well known to exhibit a giant resonance in its photon absorption spectrum near 20 eV. This is associated with a surface plasmon, where delocalized electrons oscillate as a whole relative to the ionic cage. Absolute photoionization cross-section measurements for C+60, C2+60, and C3+60 ions in the 17-75 eV energy range show an additional resonance near 40 eV. Time-dependent density functional calculations confirm the collective nature of this feature, which is characterized as a dipole-excited volume plasmon made possible by the special fullerene geometry.

Semi-Automated Detection of Trace Explosives in Fingerprints on Strongly Interfering Surfaces with Raman Chemical Imaging:

Abstract: We have previously demonstrated the use of wide-field Raman chemical imaging (RCI) to detect and identify the presence of trace explosives in contaminated fingerprints. In this current work we demonstrate the detection of trace explosives in contaminated fingerprints on strongly Raman scattering surfaces such as plastics and painted metals using an automated background subtraction routine. We demonstrate the use of partial least squares subtraction to minimize the interfering surface spectral signatures, allowing the detection and identification of explosive materials in the corrected Raman images. The resulting analyses are then visually superimposed on the corresponding bright field images to physically locate traces of explosives. Additionally, we attempt to address the question of whether a complete RCI of a fingerprint is required for trace explosive detection or whether a simple non-imaging Raman spectrum is sufficient. This investigation further demonstrates the ability to nondestructively identify explosives on fingerprints present on commonly found surfaces such that the fingerprint remains intact for further biometric analysis.

Raman chemical imaging of explosive-contaminated fingerprints.

Abstract: Raman chemical imaging (RCI) has been used to detect and identify explosives in contaminated fingerprints Bright-field imaging is used to identify regions of interest within a fingerprint, which can then be examined to determine their chemical composition using RCI and fluorescence imaging Results are presented where explosives in contaminated fingerprints are identified and their spatial distributions are obtained Identification of explosives is obtained using Pearson's cosine cross-correlation technique using the characteristic region (500–1850 cm−1) of the spectrum This study shows the ability to identify explosives nondestructively so that the fingerprint remains intact for further biometric analysis Prospects for forensic examination of contaminated fingerprints are discussed

Kinetics and Reaction Mechanisms of Thiophenol Adsorption on Gold Studied by Surface-Enhanced Raman Spectroscopy

Abstract: Thiophenol is commonly used as a model system for surface-enhanced Raman scattering (SERS) of molecules due to the strong affinity of the −SH group toward noble metal surfaces. By performing time-, temperature-, and pH-dependent measurements of thiophenol adsorption on commercial nanostructured gold SERS substrates, we have observed both physisorption and chemisorption processes. These two distinct adsorption regimes were found dependent on the pH which controlled the ionization state of thiophenol in an aqueous medium. At low pH the sulfhydryl proton remains bound, and the kinetic adsorption profile obtained from the SERS intensity follows a sigmoid-shaped curve with an initially slow adsorption rate that deviates from a Langmuir profile. In addition, from temperature-dependent measurements, a near zero value for the activation energy is obtained, indicating that physisorption is the rate-limiting step. At high pH, where the sulfhydryl proton becomes detached, the kinetic adsorption profile follows a cla...

Recoil-ion and electron momentum spectroscopy: reaction-microscopes

Abstract: Recoil-ion and electron momentum spectroscopy is a rapidly developing technique that allows one to measure the vector momenta of several ions and electrons resulting from atomic or molecular fragmentation. In a unique combination, large solid angles close to 4π and superior momentum resolutions around a few per cent of an atomic unit (a.u.) are typically reached in state-of-the art machines, so-called reaction-microscopes. Evolving from recoil-ion and cold target recoil-ion momentum spectroscopy (COLTRIMS), reaction-microscopes—the `bubble chambers of atomic physics'—mark the decisive step forward to investigate many-particle quantum-dynamics occurring when atomic and molecular systems or even surfaces and solids are exposed to time-dependent external electromagnetic fields. This paper concentrates on just these latest technical developments and on at least four new classes of fragmentation experiments that have emerged within about the last five years. First, multi-dimensional images in momentum space brought unprecedented information on the dynamics of single-photon induced fragmentation of fixed-in-space molecules and on their structure. Second, a break-through in the investigation of high-intensity short-pulse laser induced fragmentation of atoms and molecules has been achieved by using reaction-microscopes. Third, for electron and ion-impact, the investigation of two-electron reactions has matured to a state such that the first fully differential cross sections (FDCSs) are reported. Fourth, comprehensive sets of FDCSs for single ionization of atoms by ion-impact, the most basic atomic fragmentation reaction, brought new insight, a couple of surprises and unexpected challenges to theory at keV to GeV collision energies. In addition, a brief summary on the kinematics is provided at the beginning. Finally, the rich future potential of the method is briefly envisaged.

Impact of hollow-atom formation on coherent x-ray scattering at high intensity

Abstract: X-ray free-electron lasers (FELs) are promising tools for structural determination of macromolecules via coherent x-ray scattering. During ultrashort and ultraintense x-ray pulses with an atomic-scale wavelength, samples are subject to radiation damage and possibly become highly ionized, which may influence the quality of x-ray scattering patterns. We develop a toolkit to treat detailed ionization, relaxation, and scattering dynamics for an atom within a consistent theoretical framework. The coherent x-ray scattering problem including radiation damage is investigated as a function of x-ray FEL parameters such as pulse length, fluence, and photon energy. We find that the x-ray scattering intensity saturates at a fluence of $~$${10}^{7}$ photon/\AA{}${}^{2}$ per pulse but can be maximized by using a pulse duration much shorter than the time scales involved in the relaxation of the inner-shell vacancy states created. Under these conditions, both inner-shell electrons in a carbon atom are removed, and the resulting hollow atom gives rise to a scattering pattern with little loss of quality for a spatial resolution $g1$ \AA{}. Our numerical results predict that in order to scatter from a carbon atom 0.1 photon per x-ray pulse, within a spatial resolution of 1.7 \AA{}, a fluence of $1\ifmmode\times\else\texttimes\fi{}{10}^{7}$ photons/\AA{}${}^{2}$ per pulse is required at a pulse length of 1 fs and a photon energy of 12 keV. By using a pulse length of a few hundred attoseconds, one can suppress even secondary ionization processes in extended systems. The present results suggest that high-brightness attosecond x-ray FELs would be ideal for single-shot imaging of individual macromolecules.

Atomic cluster collisions

Abstract: Atomic cluster collisions are a field of rapidly emerging research interest by both experimentalists and theorists. The international symposium on atomic cluster collisions (ISSAC) is the premier forum to present cutting-edge research in this field. It was established in 2003 and the most recent conference was held in Berlin, Germany in July of 2011. This Topical Issue presents original research results from some of the participants, who attended this conference. This issues specifically focuses on two research areas, namely Clusters and Fullerenes in External Fields and Nanoscale Insights in Radiation Biodamage.

Developments in spontaneous and coherent Raman scattering microscopic imaging for biomedical applications

Abstract: First, the potential role of Raman-based techniques in biomedicine is introduced. Second, an overview about the instrumentation for spontaneous and coherent Raman scattering microscopic imaging is given with a focus of recent developments. Third, imaging strategies are summarized including sequential registration with laser scanning microscopes, line imaging and global or wide-field imaging. Finally, examples of biomedical applications are presented in the context of single cells, laser tweezers, tissue sections, biopsies and whole animals.