Photocurrent generation in polymer-fullerene bulk heterojunctions

The photocurrent in conjugated polymer-fullerene blends is dominated by the dissociation efficiency of bound electron-hole pairs at the donor-acceptor interface. A model based on Onsager's theory of geminate charge recombination explains the observed field and temperature dependence of the photocurrent in PPV:PCBM blends. At room temperature only 60% of the generated bound electron-hole pairs are dissociated and contribute to the short-circuit current, which is a major loss mechanism in photovoltaic devices based on this material system.     

Multiple solid-phase microextraction

Theoretical aspects of multiple solid-phase microextraction are described and the principle is illustrated with the extraction of lidocaine from aqueous solutions. With multiple extraction under non-equilibrium conditions considerably less time is required in order to obtain an extraction yield that is equal to that of one extraction at equilibrium. On the other side, the extraction yield can be increased if multiple extraction is performed with the same total time as is needed for one extraction at equilibrium time. The effect of multiple extraction is strongly dependent on the value of the partition constant and for practical use the length of the desorption time is important. A good agreement between theoretical and experimental data has been obtained. Chromatograms are presented showing the potential of multiple solid-phase microextraction.     

Giant muon knight shifts in antimony and antimony alloys

The Knight shift K_μ at the positive muon has been measured as a function of magnetic field, temperature, crystal orientation and alloyed impurity (bismuth or tin) in antimony. The anomalously large and anisotropic K_μ in pure Sb at low temperature has been confirmed and shown to be independent of magnetic field up to 9 kG; its anisotropic part is found to have the same strong temperature dependence as its isotropic component. The addition of 6.3 at.% Bi significantly reduces both K_μ and its anisotropy, but enhances their temperature dependence. The addition of 12.5 at.% Bi, or, more dramatically, as little as 0.3 at.% Sn to antimony is sufficient to reduce K_μ to a small value, effectively eliminating the anomalous behaviour.     

Studies of parity and time reversal symmetries in neutron scattering from165Ho

We describe searches for parity and time reversal violations in the scattering of polarized neutrons from polarized and aligned¹⁶⁵Ho targets. We have completed a search with 7.1 and 11.0 MeV neutrons for P_oddT_odd terms in the elastic scattering forward amplitude of the form s. (I×K), wheres is the neutron spin,I is the target spin andk is the neutron momentum vector. The target was a single crystal of holmium, polarized horizontally along itsb axis by a 1 Tesla magnetic field. The neutrons were polarized vertically. Differences in the neutron transmission were measured for neutrons with spins parallel (antiparallel) toI×k. The P,T violating analyzing powers were found to be consistent with zero at the few 10⁻³ level: ρ_P,T(7.1 MeV)=−0.88 (±2.02) x 10⁻³, ρ_P,T(11.0 MeV)=−0.4 (±2.88) x 10⁻³. We have also attempted to find enhancements with MeV neutrons in P-violation due to the term s\k. We are preparing an aligned target cryostat for investigations of P_evenT_odd terms {bd(I\k)(I×k)\s} in neutron scattering. The target will be a single crystal cylinder of¹⁶⁵Ho cooled to 100 mK in a bath of liquid helium and rotated by a shaft from a room temperature stepping motor. The cylinder will be oriented vertically and the alignment (c) axis oriented horizontally. Warming or rotation of the sample allows one to separate effects that mimic the sought-after time reversal violating term.     

Preparation and analysis of a river sediment Standard Reference Material for the determination of trace organic constituents

Summary A river sediment Standard Reference Material (SRM) has been prepared and analyzed for determination of the concentrations of trace organic constituents. SRM 1939, Polychlorinated Biphenyls (PCBs) in River Sediment A, has been certified for the concentrations of three PCB congeners using the results obtained from capillary column gas chromatography with electron capture detection (GC-ECD) and from multidimensional (dual column) capillary gas chromatography with mass spectrometric detection (MCGC-MSD). For SRM certification, two independent analytical procedures are usually required. If only one analytical technique is used or if the procedures are not independent, then the concentrations are reported as noncertified or informational values rather than certified values. Noncertified values for 14 additional PCB congeners and five chlorinated pesticides, determined by GC-ECD, are also reported as well as noncertified concentrations for five polycyclic aromatic hydrocarbons (PAHs), determined using gas chromatography with mass spectrometric detection (GC-MSD). SRM 1939 complements SRM 1941, Organics in Marine Sediment, since both materials have 12 PCB congeners, five PAHs and five chlorinated pesticides in common. However, the concentrations differ by an order of magnitude for PAHs, and from one to over two orders of magnitude for the PCB congeners and chlorinated pesticides.     

Dehydration of solute-lipid systems: hydration forces analysis

Sorption isotherms were obtained for a range of lipid/sugar/water mixtures. These were analysed using a simple hydration forces formalism. The results demonstrate that this simple analysis can be used to estimate dehydration parameters for these relatively complex systems. This in turn provides some insight into the location and role of sugars in the hydration behaviour of lipid systems. The relevance of these results to the phase behaviour of lipid/sugar mixtures during dehydration are discussed.