Observation of exclusive DVCS in polarized electron beam asymmetry measurements

We report the first results of the beam spin asymmetry measured in the reaction e + p -> e + p + gamma at a beam energy of 4.25 GeV. A large asymmetry with a sin(phi) modulation is observed, as predicted for the interference term of Deeply Virtual Compton Scattering and the Bethe-Heitler process. The amplitude of this modulation is alpha = 0.202 +/- 0.028. In leading-order and leading-twist pQCD, the alpha is directly proportional to the imaginary part of the DVCS amplitude.Comment: 6 pages, 5 figure

A Kinematically Complete Measurement of the Proton Structure Function F2 in the Resonance Region and Evaluation of Its Moments

We measured the inclusive electron-proton cross section in the nucleon resonance region (W < 2.5 GeV) at momentum transfers Q**2 below 4.5 (GeV/c)**2 with the CLAS detector. The large acceptance of CLAS allowed for the first time the measurement of the cross section in a large, contiguous two-dimensional range of Q**2 and x, making it possible to perform an integration of the data at fixed Q**2 over the whole significant x-interval. From these data we extracted the structure function F2 and, by including other world data, we studied the Q**2 evolution of its moments, Mn(Q**2), in order to estimate higher twist contributions. The small statistical and systematic uncertainties of the CLAS data allow a precise extraction of the higher twists and demand significant improvements in theoretical predictions for a meaningful comparison with new experimental results.Comment: revtex4 18 pp., 12 figure

Tensor Polarization of the phi meson Photoproduced at High t

As part of a measurement of the cross section of $\phi$ meson photoproduction to high momentum transfer, we measured the polar angular decay distribution of the outgoing $K^+$ in the channel $\phi \to K^+K^-$ in the $\phi$ center-of-mass frame (the helicity frame). We find that s-channel helicity conservation (SCHC) holds in the kinematical range where $t$-channel exchange dominates (up to $-t \sim 2.5$ GeV$^2$ for $E_{\gamma}$=3.6 GeV). Above this momentum, $u$-channel production of a $\phi$ meson dominates and induces a violation of SCHC. The deduced value of the $\phi NN$ coupling constant lies in the upper range of previously reported values.Comment: 6 pages; 5 figure

Development of wet environmental TEM (wet-ETEM) for in situ studies of liquid-solid catalyst reactions on the nanoscale

We present the development of in situ wet environmental transmission electron microscopy (Wet-ETEM) for direct probing of controlled liquid–catalyst reactions at operating temperatures on the nanoscale. The first nanoscale imaging and electron diffraction of dynamic liquid hydrogenation and polymerization reactions in the manufacture of polyamides reported here opens up new opportunities for high resolution studies of a wide range of solution–solid and solution–gas–solid reactions in the chemical and biological sciences

Surface atomic defect structures and growth of gold nanorods

We present atomic and defect structural studies of technologically important gold nanorods synthesized by a wet chemical process. Our surface atomic structural studies and electron nanodiffraction from single nanorods have provided the first direct evidence of the stabilization of the highly unstable (110) surface by surfactant molecules. The insights into surface defect structures have important implications in the applications of nanorods in the molecular device technology. The origin and the development of the growth process of nanorods have been inferred from the results

In situ nanoscale wet imaging of the heterogenous catalyzation of nitriles in a solution phase: novel hydrogenation chemistry through nanocatalysts on nanosupports

Wet-environmental transmission electron microscopy studies of heterogeneous hydrogenation of complex nitriles in a liquid phase over new mesoporous cobalt-promoted ruthenium nanocatalysts on reducible nanotitania supports are presented. The desorbed organic products in the dynamic liquid phase hydrogenation are imaged situ on the nanoscale. The direct studies on the “nanocomposite” catalysts are correlated with parallel reaction chemistry measurements. They demonstrate high hydrogenation activity at low operating temperatures in the presence of atomic scale anion vacancy defects associated with Lewis acid sites at the nanosupport surface and an electronic and synergistic contribution to the promoter mechanism. The combined synergistic effect between the two metals and the interaction with the reduced nanosupport leading to an electronic modification lead to highly reactive site for the hydrogenation catalysis. The results illustrate novel selective hydrogenation chemistry with mesoporous nanocatalyst systems on nanosupports