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Characterization of Hafnia Powder Prepared from an Oxychloride Sol–Gel


  • T. Troczynski—contributing editor

  • Based on part of the thesis submitted by C. M. McGilvery for the Ph.D. degree in Nanomaterials, Imperial College London, London, SW7 2AZ. 2008.
    This work was financially supported by the Engineering and Physical Sciences Research Council (EPSRC) grant number GR/S41036. A portion of this research at Oak Ridge National Laboratory's Center for Nanophase Materials Sciences was sponsored by the Scientific User Facilities Division, Office of Basic Energy Sciences, U.S. Department of Energy.

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Hafnium-containing compounds are of great importance to the semiconductor industry as a high-κ gate dielectric to replace silicon oxynitrides. Here, the crystallization processes and chemistry of bulk hafnia powders are investigated, which will aid in interpretation of reactions and crystallization events occurring in thin films used as gate dielectrics. Amorphous hafnia powder was prepared via a sol–gel route using the precursor HfOCl2·H2O. The powders were subjected to various heat treatments and analyzed using X-ray diffraction and thermal analysis techniques. A large change in the crystallization pathway was found to occur when the sample was heated in an inert environment compared with air. Instead of the expected monoclinic phase, tetragonal hafnia also formed under these conditions and was observed up to temperatures of ∼760°C. The tetragonal particles eventually transform into monoclinic hafnia on further heating. Possible mechanisms for the crystallization of tetragonal hafnia are discussed. It is proposed that, in an inert environment, tetragonal hafnia is stabilized due to the presence of oxygen vacancies, formed by the reduction of HfIV to HfIII. As the temperature increases the crystal grows until there are too few oxygen vacancies left in the structure to continue stabilizing the tetragonal phase, and hence transformation to monoclinic hafnia occurs.

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