Coulomb explosion imaging of small molecules.

Most of our knowledge of the structures of free molecules comes from indirect observations that focus on other properties (for example, energy or mass spectra) that depend on structure. Recently, a new method has been developed that instead yields geometrical images of individual molecules. This method takes advantage of the large Coulomb repulsion of the nuclei within molecules rapidly stripped of their electrons. The first experiments with this new technique have already revealed structural images of several important species, such as positively charged methane ions.

Electron photodetachment cross sections of small carbon clusters: evidence for nonlinear isomers.

Absolute cross sections for photodetachment of negative carbon clusters are reported for Cn (n = 3, ..., 8). The results indicate that various neutral isomers exist, some with electron affinities as low as 1 electron volt. The method of production plays an important role in the characteristics of carbon clusters.

Spin selectivity in electron transmission through self-assembled monolayers of double-stranded DNA.

In electron-transfer processes, spin effects normally are seen either in magnetic materials or in systems containing heavy atoms that facilitate spin-orbit coupling. We report spin-selective transmission of electrons through self-assembled monolayers of double-stranded DNA on gold. By directly measuring the spin of the transmitted electrons with a Mott polarimeter, we found spin polarizations exceeding 60% at room temperature. The spin-polarized photoelectrons were observed even when the photoelectrons were generated with unpolarized light. The observed spin selectivity at room temperature was extremely high as compared with other known spin filters. The spin filtration efficiency depended on the length of the DNA in the monolayer and its organization.

Chirality-induced spin-selective properties of self-assembled monolayers of DNA on gold.

Here we show that self-assembled monolayers on gold of double-stranded DNA oligomers interact with polarized electrons similarly to a strong and oriented magnetic field. The direction of the field for right-handed DNA is away from the substrate. Moreover, the layer shows very high paramagnetic susceptibility. Interestingly, thiolated single-stranded DNA oligomers on gold do not show this effect. The new findings are rationalized based on recent results in which high paramagnetism was measured for diamagnetic films adsorbed on diamagnetic substrates.

Laser displacement sensor with application to gravitational radiation detection.

The principles of operation of a novel laser displacement sensor are described. The intended application of the sensor is to measure displacements induced by gravitational radiation. The laser sensor is composed of three coupled cavities, defined by two laser mirrors and the mirrors of a Fabry-Perot etalon placed inside the laser cavity. The laser is forced to oscillate in two longitudinal modes by a Fox-Smith internal mode selector. It is shown that the laser system can be made to operate in a condition where the beat frequency between these modes has an enhanced sensitivity to relative displacements between the etalon mirrors. A He-Ne laser displacement sensor was constructed, and a displacement sensitivity of 4.6 x 10(12) Hz/cm was obtained. This value is shown to be in good agreement with the value predicted by a theoretical analysis of the sensor performance.

Two- and three-body kinematical correlation in the dissociative recombination of H(3)(+).

Fragmentation patterns for dissociative recombination of the triatomic hydrogen molecular ion H(3)(+) in the vibrational ground state have been measured using the storage ring technique and molecular fragment imaging. A broad distribution of vibrational states in the H(2) fragment after two-body dissociation and a large predominance of nearly linear momentum geometries after three-body dissociation are found. The fragmentation results are directly contrasted with Coulomb explosion imaging data on the initial H(3)(+) geometry, compared to existing wave-packet calculations, and considered in the light of a simple physical picture.

Dissociative recombination of HD+ in selected vibrational quantum states

Rate coefficients for dissociative recombination of HD+ in selected vibrational states have been measured by a combination of two molecular fragment imaging methods by using the heavy-ion storage ring technique. Recombination fragment imaging yields state-to-state reaction rates. These rates are converted to rate coefficients by using vibrational level populations of the stored ion beam, derived from nuclear coordinate distributions measured on extracted ions. The results show strongly increasing rate coefficients for high vibrational excitation, where additional dissociation routes open up, in agreement with a theoretical calculation. Very low rate coefficients are found for certain, isolated vibrational states.