Jpn. J. Appl. Phys. 47 (2008) pp. 7975-7979  |Previous Article| |Next Article|  |Table of Contents|
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Approximants in the Ag–In–M and Au–Sn–M (M = Ca or Rare Earth Metals) Systems

Yoshiki Morita and An Pang Tsai1

Department of Materials Processing, Graduate School of Engineering, Tohoku University, Sendai 980-8579, Japan
1Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, Sendai 980-8577, Japan

(Received April 19, 2008; accepted July 4, 2008; published online October 17, 2008)

Formation of 1/1 Yb–Cd type approximants has been verified in the Ag–In–RE (RE: rare earth metals) system for RE = Tm, Tb, Er, Dy, Gd, Pr, Ce, or Eu. The compositions of the 1/1 approximants determined by wavelength dispersive X-ray analysis (WDX), are in the range of 42–48 at. % Ag, 38–42 at. % In, and 14–15 at. % REs. By employing the empirical rule of e/a∼2.0, where e/a is the valence electron concentration, a number of approximants are newly found in the Au–Sn–RE systems for RE = Sm, Pr, Ce, Dy, Tb, Gd, or Eu, where the 1/1 approximants are formed in the range of 61–64 at. % Au, 20–23 at. % Sn, and 14–15 at. % REs. The 2/1 approximants only form in Ag43In43Eu14 and Au60Sn25M15 for M = Eu, Yb, or Ca, where the atomic size for Eu, Yb, and Ca is larger than that for the other REs and they are all divalent. Basically, the 2/1 and 1/1 approximants share the same e/a as the quasicrystals found in the In–Ag–M, Au–Sn–M, and Cd–M groups. It is likely that the phase selection among the quasicrystalline and the 1/1 and 2/1 approximant phases is dominated by the effective atomic size factor, Rr,e.

URL: http://jjap.jsap.jp/link?JJAP/47/7975/
DOI: 10.1143/JJAP.47.7975


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References | Citing Articles (6)

  1. A. P. Tsai, J. Q. Guo, E. Abe, H. Takakura, and T. J. Sato: Nature 408 (2000) 537.
  2. J. Q. Guo, E. Abe, and A. P. Tsai: Phys. Rev. B 62 (2000) R14605[APS].
  3. A. Palenzona: J. Less-Common Met. 25 (1971) 367.
  4. C. P. Gómez and S. Lidin: Angew. Chem., Int. Ed. 40 (2001) 4037.
  5. H. Takakura, C. P. Gómez, A. Yamamoto, M. De Boissieu, and A. P. Tsai: Nat. Mater. 6 (2007) 58.
  6. M. Armbrüster and S. Lidin: J. Alloys Compd. 307 (2000) 141.
  7. R. Tamura, Y. Murao, S. Takeuchi, M. Ichihara, M. Isobe, and Y. Ueda: Jpn. J. Appl. Phys. 41 (2002) L524[JSAP].
  8. C. P. Gómez and S. Lidin: Chem.–Eur. J. 10 (2004) 3279.
  9. J. Q. Guo and A. P. Tsai: Philos. Mag. Lett. 82 (2002) 349.
  10. J. F. Ruan, K. H. Kuo, J. Q. Guo, and A. P. Tsai: J. Alloys Compd. 370 (2004) L23.
  11. C. P. Gomez: in preparation for publication.
  12. Q. Lin and J. D. Corbett: J. Am. Chem. Soc. 129 (2007) 6789[CrossRef].
  13. A. Singh, J. Q. Guo, and A. P Tsai: Mater. Sci. Eng. A 449–451 (2007) 991.
  14. P. Boulet, D. Mazzone, H. Noel, P. Rogl, and R. Ferro: J. Alloys Compd. 307 (2000) 141.
  15. D. E. Sands, Q. C. Johnson, O. H. Krikorian, and K. L. Kromholtz: Acta Crystallogr. 15 (1962) 1191.
  16. S. Kenzari, V. Demange, P. Boulet, M. C. de Weerd, J. Ledieu, J. M. Dubois, and V. Fournée: J. Phys.: Condens. Matter 20 (2008) 095218[IoP STACKS].
  17. H. Kaneko, Y. Arichika, and T. Ishimasa: Philos. Mag. Lett. 81 (2001) 777.
  18. S. Kashimoto, R. Maezawa, Y. Kasano, T. Mitani, and T. Ishimasa: Jpn. J. Appl. Phys. 42 (2003) L1268[JSAP].
  19. R. Maezawa, S. Kashimoto, and T. Ishimasa: Philos. Mag. Lett. 84 (2004) 215.

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