Due to the unprecedented rapid increase of their power conversion efficiency, hybrid organic-inorganic perovskites CH 3 NH 3 PbX 3 (X = I, Br, Cl) can potentially revolutionize the world of solar cells. However, despite tremendous research activity, the origin of the exceptionally large diffusion length of their photogenerated charge carriers, that is, their low recombination rate, remains elusive. Using frequency and temperature-dependent dielectric measurements across the entire frequency spectrum, it is shown that the dielectric constant conserves very high values (>27) for frequencies below 1 THz in all three halides. This efficiently prevents photocarrier trapping and their recombination owing to the strong screening of charged entities. By combining ultrasonic and Raman spectroscopy with dielectric analysis, similarly large contributions to the dielectric constant are attributed to the dipolar disorder of the CH 3 NH 3 + cations as well as lattice dynamics in the gigahertz range yielding dielectric constants of ε stat = 62 for the iodide, 58 for the bromide, and about 45 for the chloride below 1 GHz at room temperature. Disorder continuously reduces for decreasing temperature. Dipole dynamics prevail in the intermediate tetragonal phase. The low-temperature orthorhombic state is antipolar. No indications of ferroelectricity are found.

We report intense terahertz emission from lead zirconate titanate (PZT) tubular nanostructures, which have a wall thickness around 40 nm and protrude on n-type Si substrates. Such emission is totally absent in flat PZT films or bulk; hence the effect is attributed to the nanoscale geometry of the tubes. The terahertz radiation is emitted within 0.2 ps, and the spectrum exhibits a broad peak from 2 to 8 THz. This is a gap in the frequency spectrum of conventional semiconductor terahertz devices, such as ZnTe, and an order of magnitude higher frequency peak than that in the well-studied p-InAs, due to the abnormally large carrier concentration gradient in the nanostructured PZT. The inferred mechanism is optical rectification within a surface accumulation layer, rather than the Dember effect. The terahertz emission is optically pumped, but since the tubes exhibit ferroelectric switching, electrically driven emission may also be possible. EPR reveals 02 molecules adsorbed onto the nanotubes, which may play some role in the emission.

The conditions for electroless nickel‐boron plating, the process mechanism, and the structure of the alloys as‐plated and after annealing at 150°–700°C were investigated. A correlation of the mechanical and magnetic properties with the changes of phase structure was established.

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