Biomedical subjects

Stephen R Leone

Publications and source records attributed to Stephen R Leone.

24 records · Page 2Linked to original sources

PubMed2005

Direct determination of the ionization energies of FeO and CuO with VUV radiation.

Photoionization efficiency curves were measured for gas-phase FeO and CuO using tunable vacuum-ultraviolet radiation at the Advanced Light Source. The molecules are prepared using laser ablation of a metal-oxide powder in a novel high-repetition-rate source and are thermally moderated in a supersonic expansion. These measurements provide the first directly measured ionization energy for CuO, IE(CuO)=9.41 +/- 0.01 eV. The direct measurement also gives a greatly improved ionization energy for FeO, IE(FeO) = 8.56 +/- 0.01 eV. The ionization energy connects the dissociation energies of the neutral and cation, leading to a refined bond strength for the FeO cation: D0(Fe(+)-O)=3.52 +/- 0.02 eV. A dramatic increase in the photoionization cross section at energies of 0.36 eV above the threshold ionization energy is assigned to autoionization and direct ionization involving one or more low-lying quartet states of FeO+. The interaction between the sextet ground state and low-lying quartet states of FeO+ is key to understanding the oxidation of hydrogen and methane by FeO+, and these experiments provide the first experimental observation of the low-lying quartet states of FeO+.

Computer Simulation↗

PubMed2005

Ultrafast wavelength-dependent lasing-time dynamics in single ZnO nanotetrapod and nanowire lasers.

The ultrafast lasing dynamics of single zinc oxide nanotetrapods and nanowires are investigated by two-color femtosecond excitation/optical injection spectroscopy. The transient spectral gain induced by time-delayed optical injection pulses (400 nm) is used to investigate the spectrally and temporally resolved lasing properties in a single tetrapod or nanowire laser excited by 267-nm pulses. The lasing output pulse exhibits a faster lasing decay time than the carrier decays due to the superlinear dependence of the lasing on the carrier density. Lasing at the low-energy side of the gain bandwidth (392 nm) has a full width at half maximum (fwhm) for stimulated emission of 1.7 ps. Lasing at 390 nm, the high-energy side of the gain bandwidth, has a fwhm of 2.1 ps for a single example nanowire. The change in lasing dynamics as a function of wavelength is affected by band gap renormalization, since lasing in the electron-hole plasma regime depends not only on the carrier density but also on the band gap shift with carrier density.

Journal Article↗

PubMed2005

Nanometer-scale optical imaging of epitaxially grown GaN and InN islands using apertureless near-field microscopy.

Nanometer-scale chemical imaging of epitaxially grown gallium nitride (GaN) and indium nitride (InN) islands is performed using scattering-type apertureless near-field scanning optical microscopy (ANSOM). The scattering of 633 nm laser radiation is modulated by an oscillating metallic probe, and the scattered radiation is detected by homodyne amplification, followed by high-harmonic demodulation, yielding optical near-field scattering maps with a spatial resolution better than 30 nm. The image contrast between InN and GaN, and the tip-sample distance dependence, can be qualitatively explained by a simple dipole-coupling model. The ANSOM images of InN and GaN also show structures that are absent in the topographic counterpart, and these substructures are explained by the variations of the local dielectric environment of InN and GaN.

Journal Article↗

PubMed2005

Vibrational distributions of the CO(v) products of the C2H2 + O(3P) and HCCO + O(3P) reactions studied by FTIR emission.

The C2H2 + O(3P) and HCCO + O(3P) reactions are investigated using Fourier transform infrared (FTIR) emission spectroscopy. The O(3P) radicals are produced by 193 nm photolysis of an SO2 precursor or microwave discharge in O2. The HCCO radical is either formed in the first step of the C2H2 + O(3P) reaction or by 193 nm photodissociation of ethyl ethynyl ether. Vibrationally excited CO and CO2 products are observed. The microwave discharge experiment [C2H2 + O(3P)] shows a bimodal distribution of the CO(v) product, which is due to the sequential C2H2 + O(3P) and HCCO + O(3P) reactions. The vibrational distribution of CO(v) from the HCCO + O(3P) reaction also shows its own bimodal shape. The vibrational distribution of CO(v) from C2H2 + O(3P) can be characterized by a Boltzmann plot with a vibrational temperature of approximately 2400 +/- 100 K, in agreement with previous results. The CO distribution from the HCCO + O(3P) reaction, when studied under conditions to minimize other processes, shows very little contamination from other reactions, and the distribution can be characterized by a linear combination of Boltzmann plots with two vibrational temperatures: 2320 +/- 40 and 10 300 +/- 600 K. From the experimental results and previous theoretical work, the bimodal CO(v) distribution for the HCCO + O(3P) reaction suggests a sequential dissociation process of the HC(O)CO++ --> CO + HCO; HCO --> H + CO.

Journal Article↗

PubMed2005

The influence of intense control laser pulses on homodyne-detected rotational wave packet dynamics in O2 by degenerate four-wave mixing.

We illustrate how the preparation and probing of rotational Raman wave packets in O(2) detected by time-dependent degenerate four-wave mixing (TD-DFWM) can be manipulated by an additional time-delayed control pulse. By controlling the time delay of this field, we are able to induce varying amounts of additional Rabi cycling among multiple rotational states within the system. The additional Rabi cycling is manifested as a change in the signal detection from homodyne detected to heterodyne detected, depending on the degree of rotational alignment induced. At the highest laser intensities, Rabi cycling among multiple rotational states cannot account for the almost complete transformation to a heterodyne-detected signal, suggesting a second mechanism involving ionization. The analysis we present for these effects, involving the formation of static alignment by Rabi cycling at moderate laser intensities and possibly ion gratings at the highest intensities, appears to be consistent with the experimental findings and may offer viable explanations for the switching from homodyne to heterodyne detection observed in similar DFWM experiments at high laser field intensities (>10(13) W/cm(2)).

Journal Article↗

PubMed2005

Light scattering of ultrafine silica particles by VUV synchrotron radiation.

Vacuum ultraviolet (VUV) light scattering from ultrafine silica particles is studied with an aerosol instrument recently established at the Advanced Light Source (ALS) in Berkeley. Silica particles, size-selected by a differential mobility analyzer, are introduced into vacuum through a set of aerodynamic lenses to form a particle beam. The scattered photons from the crossing area of the VUV synchrotron beam and particle beam are detected with a rotatable VUV photon detector. The angular distributions of scattered photons (ADSP) originating from 70, 100, 200 nm diameter silica particles are measured with 145.9 and 118.1 nm synchrotron radiation. These angular distributions show strong forward scattering. The measured ADSPs are consistent with simulation of Mie scattering. The refractive indices of silica particles, 2.6 + 1.1i and 1.6 + 0.0001i for 118.1 and 145.9 nm, respectively, are obtained by fitting the measured ADSPs; the least average percentage deviations are 18% and 6%, respectively. The scattered fluxes at widely different wavelengths (visible versus VUV) also exhibit clear size sensitivity. Under comparable experimental conditions of photon fluxes and detection efficiencies, limits of particle size detection of 70 and 250 nm are obtained, respectively, when using 118.1 and 532 nm illumination. As anticipated, VUV scattering is a more sensitive probe for ultrafine particles, which will find application in detection of these ubiquitous species beyond the confines of a laboratory.

Light↗