Field collapse due to band-tail charge in amorphous silicon solar cells

It is common for the fill factor to decrease with increasing illumination intensity in hydrogenated amorphous silicon solar cells. This is especially critical for thicker solar cells, because the decrease is more severe than in thinner cells. Usually, the fill factor under uniformly absorbed red light changes much more than under strongly absorbed blue light. The cause of this is usually assumed to arise from space charge trapped in deep defect states. The authors model this behavior of solar cells using the Analysis of Microelectronic and Photonic Structures (AMPS) simulation program. The simulation shows that the decrease in fill factor is caused by photogenerated space charge trapped in the band-tail states rather than in defects. This charge screens the applied field, reducing the internal field. Owing to its lower drift mobility, the space charge due to holes exceeds that due to electrons and is the main cause of the field screening. The space charge in midgap states is small compared with that in the tails and can be ignored under normal solar-cell operating conditions. Experimentally, the authors measured the photocapacitance as a means to probe the collapsed field. They also explored the light intensity dependence of photocapacitance and explain the decrease of FF with the increasing light intensity

Quantum mechanical virial theorem in systems with translational and rotational symmetry

Generalized virial theorem for quantum mechanical nonrelativistic and relativistic systems with translational and rotational symmetry is derived in the form of the commutator between the generator of dilations G and the Hamiltonian H. If the conditions of translational and rotational symmetry together with the additional conditions of the theorem are satisfied, the matrix elements of the commutator [G, H] are equal to zero on the subspace of the Hilbert space. Normalized simultaneous eigenvectors of the particular set of commuting operators which contains H, J^{2}, J_{z} and additional operators form an orthonormal basis in this subspace. It is expected that the theorem is relevant for a large number of quantum mechanical N-particle systems with translational and rotational symmetry.Comment: 24 pages, accepted for publication in International Journal of Theoretical Physic

Simple Description of Pion-Pion Scattering to 1 GeV

Motivated by the 1/Nc expansion, we present a simple model of pion-pion scattering as a sum of a `current-algebra' contact term and resonant pole exchanges. The model preserves crossing symmetry as well as unitarity up to 1.2 GeV. Key features include chiral dynamics, vector meson dominance, a broad low energy scalar (sigma) meson and a `Ramsauer-Townsend' mechanism for the understanding of the 980 MeV region. We discuss in detail the `regularization' (corresponding to rescattering effects) necessary to make all these nice features work.Comment: 35 pages (LaTeX), 13 PostScript figures are included as uuencoded-compressed-ta

The inner junction protein CFAP20 functions in motile and non-motile cilia and is critical for vision

Motile and non-motile cilia are associated with mutually-exclusive genetic disorders. Motile cilia propel sperm or extracellular fluids, and their dysfunction causes primary ciliary dyskinesia. Non-motile cilia serve as sensory/signalling antennae on most cell types, and their disruption causes single-organ ciliopathies such as retinopathies or multi-system syndromes. CFAP20 is a ciliopathy candidate known to modulate motile cilia in unicellular eukaryotes. We demonstrate that in zebrafish, cfap20 is required for motile cilia function, and in C. elegans, CFAP-20 maintains the structural integrity of non-motile cilia inner junctions, influencing sensory-dependent signalling and development. Human patients and zebrafish with CFAP20 mutations both exhibit retinal dystrophy. Hence, CFAP20 functions within a structural/functional hub centered on the inner junction that is shared between motile and non-motile cilia, and is distinct from other ciliopathy-associated domains or macromolecular complexes. Our findings suggest an uncharacterised pathomechanism for retinal dystrophy, and potentially for motile and non-motile ciliopathies in general.</p

Low lying defect mode in CaF/sub 2/:Y/sup 3 +/. [Measurements to 6. 5 kbars at 4. 2/sup 0/K]

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