ABSTRACT
In the present work, we report on the investigation of low-temperature (300-5 K) thermoelectric properties of hot-pressed TiSe2, a charge-density-wave (CDW) material. We demonstrate that, with increasing hot-pressing temperature, the density of TiSe2 increases and becomes nonstoichiometric owing to the loss of selenium. X-ray diffraction, scanning electron microscopy, and transimission electron microscopy results show that the material consists of a layered microstructure with several defects. Increasing the hot-press temperature in nonstoichiometric TiSe2 leads to a reduction of the resistivity and enhancement of the Seebeck coefficient in concomitent with suppression of CDW. Samples hot-pressed at 850 °C exhibited a minimum thermal conductivity (κ) of 1.5 W/m·K at 300 K that, in turn, resulted in a figure-of-merit (ZT) value of 0.14. This value is higher by 6 orders of magnitude compared to 1.49 × 10(-7) obtained for cold-pressed samples annealed at 850 °C. The enhancement of ZT in hot-pressed samples is attributed to (i) a reduced thermal conductivity owing to enhanced phonon scattering and (ii) improved power factor (α(2)σ).
ABSTRACT
In this paper we report the thermoelectric performance of Sr intercalated TiSe(2) above 300 K. Refined x-ray diffraction, high resolution transmission electron microscopy and scanning electron microscopy images show well oriented polycrystalline grains along a (0 0 l) direction and layered growth of the sample. Intercalation of Sr in TiSe(2) shows an improved Seebeck coefficient (α) value without altering the polarity of the majority charge carrier. A drastic reduction in the thermal conductivity (κ) from 3.8 W m K(-1) to 1.2 W m K(-1) (at 650 K) was observed which is ascribed to the: (i) scattering of the phonon by natural layer interfaces, grain boundaries and lattice defects and (ii) rattling of intercalated Sr atoms among weakly bound TiSe(2) layers. This led to the maximum ZT of ~0.08 at 650 K for Sr(x)TiSe(2) (x > 0.1) which is almost twice as high as the parent TiSe(2).
ABSTRACT
ZnO nanotetrapods have been obtained in large quantities by carbothermal reduction of ZnO powder. These were characterized by X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy, transmission electron microscopy, selected area electron diffraction, UV-visible spectroscopy and photoluminescence. Electron microscopy revealed that the overall size of the tetrapods is 1.5-2 microm and legs are 30-50 nm in diameter. The size of tetrapods as well as diameter of the legs was found to increase with deposition temperature. Photoluminescence spectra revealed that green emission originating from oxygen vacancies overwhelmed that of the near-band-edge ultraviolet peak. A band gap of 3.27 eV was calculated from optical absorption spectra which agreed well with that estimated from PL spectra. Gas sensing properties of tetrapods were investigated and these were found to be 5 times more sensitive to H2S gas at room temperature in comparison to ZnO bulk polycrystalline material.
ABSTRACT
We report here the synthesis of nickel hexacyanoferrate (NiHCF) crystals using calf thymus DNA (CT-DNA) as a template. The double-stranded CT-DNA has been used as a template to self-assemble NiHCF crystals and to produce aggregates having different morphologies at different temperatures. The guided self-assembly behavior of DNA was studied at different temperatures by scanning electron microscopy. The cube-shaped crystals of NiHCF with an average diameter of 400 nm are observed along the DNA framework at room temperature; however, at higher temperatures, the morphology of NiHCF changed from open tubular to dendrimer. The intermediate temperatures show long chains (up to many micrometers) and spherical structures of NiHCF crystals. The micrometer long DNA template plays a key role in the formation of extended arrays of NiHCF crystals, suggesting that the templating action is retained even at the higher temperatures.
