Presently, the only commercially available power generating thermoelectric (TE) modules are based on bismuth telluride (Bi2Te3) alloys and are limited to a hot side temperature of 250 °C due to the melting point of the solder interconnects and/or generally poor power generation performance above this point. For the purposes of demonstrating a TE generator or TEG with higher temperature capability, we selected skutterudite based materials to carry forward with module fabrication because these materials have adequate TE performance and are mechanically robust. We have previously reported the electrical power output for a 32 couple skutterudite TE module, a module that is type identical to ones used in a high temperature capable TEG prototype. The purpose of this previous work was to establish the expected power output of the modules as a function of varying hot and cold side temperatures. Recent upgrades to the TE module measurement system built at the Fraunhofer Institute for Physical Measurement Techniques allow for the assessment of not only the power output, as previously described, but also the thermal to electrical energy conversion efficiency. Here we report the power output and conversion efficiency of a 32 couple, high temperature skutterudite module at varying applied loading pressures and with different interface materials between the module and the heat source and sink of the test system. We demonstrate a 7% conversion efficiency at the module level when a temperature difference of 460 °C is established. Extrapolated values indicate that 7.5% is achievable when proper thermal interfaces and loading pressures are used.
Coherent acoustic oscillations in Bi and Ag nanowire samples were studied with a femtosecond pump-probe technique and detection of the scattered light. The observed optical and acoustic properties reflect the nano-structure of these materials. The electronic and lattice contributions to the excitation of coherent acoustic phonons are described using a two-temperature model. The excitation is performed at different laser fluences, and the high density of optically induced excitations modifies the state of the lattice. A transient state with softening of the lattice was observed in Ag nanowire samples. DOI: 10.1103/PhysRevB.76.184301 PACS numbers: 43.35.d, 42.25.Bs, 42.50.Md, 42.62.b I
The correlation between the crystal structure and the magnetic properties of Co nanowires of diameter 65 and 200 nm fabricated by electroplating Co into the pores of anodic aluminum oxide membranes has been investigated. Strikingly different microstructures have been observed in these Co nanowires by means of x-ray diffraction and selected area electron diffraction measurements. The 65 nm thick Co nanowires are composed of long and ordered hexagonal close-packed Co grains (>5 microm), while the 200 nm thick Co nanowires are composed of submicron-long hexagonal close-packed and face-centered cubic Co grains. Correspondingly, different magnetic properties have been observed for these Co nanowires. Magnetization measurements have found that the 65 nm thick Co nanowires have a magnetic hysteresis that is significantly larger than that of the 200 nm thick Co nanowires. Spontaneous magnetic moments of the nanowires are parallel to the nanowires in the 65 nm thick Co nanowires, but they are transverse to the nanowires in the 200 nm thick Co nanowires, as observed by the magnetic force microscopy. The correlation between their different magnetic properties and microstructures is discussed.
Bi nanowires have been fabricated by electrochemical deposition into the pores of ion track etched polycarbonate membranes. Transmission electron microscopy and selected area electron diffraction measurements reveal that these Bi nanowires are single crystalline with the rhombohedral lattice structure of bulk Bi at ambient pressure. We have measured the temperature dependence of the resistance and I-V characteristics at various magnetic fields on these Bi nanowires. These measurements show clear evidence for superconductivity below 0.64 K.
Coherent acoustic and optical phonon oscillations in Bi nanowire samples were studied with a femtosecond pump-probe technique. Laser pulses of 50 fs excited simultaneously acoustic oscillations at a frequency of about 9.5 GHz and optical phonons in the terahertz range. The transmission signal of nanowires on a glass substrate and the signal of light scattered from freestanding nanowires were measured. The acoustic velocity in nanowires was found to be close to that of bulk polycrystalline material. The changes in the optical phonon frequency at different laser fluences were simulated taking into account excitation inhomogeneity, lattice anharmonicity, diffusion, and recombination of the carriers and gave good agreement with experimental results.
The fabrication and structure characterization of ordered nanowire-nanotube hybrid arrays embedded in porous anodic aluminum oxide (AAO) membranes are reported. Arrays of TiO(2) nanotubes were first deposited into the pores of AAO membranes by a sol-gel technique. Co nanowires were then electrochemically deposited into the TiO(2) nanotubes to form the nanowire-nanotube hybrid arrays. Scanning electron microscopy and transmission electron microscopy measurements showed a high nanowire filling factor and a clean interface between the Co nanowire and the TiO(2) nanotube. Application of these hybrids to the fabrication of ordered nanowire arrays with highly controllable geometric parameters is discussed.
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