Photoinduced Phase Transformations in Boron Nitride: New Polytypic Forms of sp(3)-Bonded (6H-and 30H-) BN

作者:Komatsu Shojiro*; Kobayashi Kazuaki; Sato Yuhei; Hirano Daisuke; Nakamura Takuya; Nagata Takahiro; Chikyo Toyohiro; Watanabe Takayuki; Takizawa Takeo; Nakamura Katsumitsu; Hashimoto Takuya
来源:Journal of Physical Chemistry C, 2010, 114(31): 13176-13186.
DOI:10.1021/jp1028728

摘要

New sp(3)-bonded polytypic forms of boron nitride (BN), namely, 6H-BN and 30H-BN, were prepared by plasma-assisted chemical vapor deposition (CVD) with an excimer laser at 193 nm being irradiated on the growing film surface Only the 6H-BN was formed by postdeposition laser irradiation (PDL) of sp(2)-bonded BN precursor films prepared by plain plasma-assisted CVD. The PDL demonstrated direct photoinduced phase transformation from sp(2)-bonded BN into denser sp(3)-bonded BN here. Typical lattice constants a and c for 6H-BN determined by X-ray diffraction were 2.501 angstrom and 12 45 angstrom, respectively, while those for 30H-BN were 2.538 angstrom and 62.61 angstrom, respectively The polytypic structures were analyzed in terms of "hexagonality" H and "close-packing" index D, and the "metastability" Delta E estimated by the first principles calculations. Linear relationships were found among the H, D, and Delta E for the polytypes of BN. AlN, and SiC, whose behavior proved to depend on the degree of ionicity in their iono-covalent bonds. The growth mechanism was discussed with regard to the "bond-strength initiative rule", according to which the local thermodynamics at very early stage of growth should favor the formation of the strongest bond available (e.g, sp(2)-hybridized bonds in BN) Our conclusion that the ultraviolet laser irradiation induced the structural relaxation of the sp(2)-bonded "metastable" phase into more stable sp(3)-bonded phases at relatively lower temperatures (850 degrees C in our case) and below atmospheric pressure appears to be consistent with the recent pressure-temperature phase diagram of BN.

  • 出版日期2010-8-12