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S. Kasiviswanathan

Researcher at Indian Institute of Technology Madras

Publications -  34
Citations -  361

S. Kasiviswanathan is an academic researcher from Indian Institute of Technology Madras. The author has contributed to research in topics: Thin film & Rutherford backscattering spectrometry. The author has an hindex of 13, co-authored 34 publications receiving 328 citations. Previous affiliations of S. Kasiviswanathan include Indian Institutes of Technology.

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A hot probe setup for the measurement of Seebeck coefficient of thin wires and thin films using integral method.

TL;DR: The Seebeck voltage obtained for constantan wire is in agreement with the NIST data for copper constantan couple and the calculated carrier concentration of ITO film from the Seebeck coefficient measurement is comparable with that obtained by electrical transport measurements.
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Correlation of Mn charge state with the electrical resistivity of Mn doped indium tin oxide thin films

TL;DR: In this paper, the authors show that Mn 2p3/2 core level can be deconvoluted into three components corresponding to Mn2+ and Mn4+ with binding energies 640.8 eV and 642.7 eV, respectively.
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Characterization of stepwise flash evaporated CuIn3Se5 films

TL;DR: In this paper, the authors used a melt-quench technique to synthesize 3 Se 5 thin films by stepwise flash evaporation from the polycrystalline powder source.
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Characterization of silver selenide thin films grown on Cr-covered Si substrates

TL;DR: In this article, the authors investigated the thermal stability of thin films formed from the solid-state reaction of Ag-Se diffusion couples on Si substrates covered with a thin Cr film, and revealed the formation of polycrystalline orthorhombic silver selenide films that remain stable without compositional change upon thermal annealing.
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Magnetic properties of ball-milled TbFe2 and TbFe2B

TL;DR: In this paper, the magnetic properties of ball-milled TbFe2 and Tb Fe2B were studied by magnetization measurements and it was found that boron occupied interstitial position in the crystal structure, just as hydrogen did.