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Reactive Ni/Ti nanolaminates

J. Appl. Phys. 106, 093505 (2009); doi:10.1063/1.3253591

Published 6 November 2009

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D. P. Adams,1,2 M. A. Rodriguez,1 J. P. McDonald,1 M. M. Bai,1,2 E. Jones, Jr.,1 L. Brewer,1 and J. J. Moore2
1Sandia National Laboratories, Albuquerque, New Mexico, 87185, USA
2Colorado School of Mines, Golden, Colorado, 80401, USA

Nickel/titanium nanolaminates fabricated by sputter deposition exhibited rapid, high-temperature synthesis. When heated locally, self-sustained reactions were produced in freestanding Ni/Ti multilayer foils characterized by average propagation speeds between ~0.1 and 1.4 m/s. The speed of a propagating reaction front was affected by total foil thickness and bilayer thickness (layer periodicity). In contrast to previous work with compacted Ni–Ti powders, no preheating of Ni/Ti foils was required to maintain self-propagating reactions. High-temperature synthesis was also stimulated by rapid global heating demonstrating low ignition temperatures (Tig)~300–400 °C for nanolaminates. Ignition temperature was influenced by bilayer thickness with more coarse laminate designs exhibiting increased Tig. Foils reacted in a vacuum apparatus developed either as single-phase B2 cubic NiTi (austenite) or as a mixed-phase structure that was composed of monoclinic B19[prime] NiTi (martensite), hexagonal NiTi2, and B2 NiTi. Single-phase, cubic B2 NiTi generally formed when the initial bilayer thickness was made small. ©2009 American Institute of Physics
History: Received 18 May 2009; accepted 26 September 2009; published 6 November 2009
Permalink: http://link.aip.org/link/?JAPIAU/106/093505/1
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KEYWORDS and PACS

Keywords
PACS
  • 81.16.-c
    Methods of nanofabrication and processing
  • 61.46.-w
    Structure of nanoscale materials
  • 81.40.Gh
    Other heat and thermomechanical treatments
  • 68.65.Ac
    Multilayers (structure and nonelectronic properties)
  • 81.15.Cd
    Deposition by sputtering
  • 81.07.-b
    Nanoscale materials and structures: fabrication and characterization
  • YEAR: 2009

PUBLICATION DATA

ISSN:
0021-8979 (print)   1089-7550 (online)
Publisher:
AIP is a member of CrossRef AIP

REFERENCES (51)

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  1. J. A. Floro, J. Vac. Sci. Technol. A 4, 631 (1986).
  2. D. M. Makowiecki and R. M. Bionta, U.S. Patent No. 5,381,944 (1995).
  3. T. W. Barbee, Jr. and T. Weihs, U.S. Patent No. 5,547,715 (1996).
  4. T. W. Barbee, Jr. and T. Weihs, U.S. Patent No. 5,538,795 (1996).
  5. T. P. Weihs and O. M. Knio, Proceedings of Ceramic Interconnect Technology Conference and Exhibition of the IMAPS, Denver, CO, 2003 (SPIE-Int. Soc. Optical Engineering, Bellingham, WA, 2003), Vol. 5231, pp. 235–239.
  6. D. Van Heerden, O. M. Knio, T. P. Weihs, and S. J. Spey, Proceedings of the 36th International Symposium on Microelectronics, Boston, MA, 2003 (International Microelectronics Society, Washington, D.C., 2003), Vol. 5288, pp. 316–321.
  7. M. Ding, F. Krieger, J. Swank, J. Poret, C. McMullan, and G. Chen, Proceedings of the 43rd Power Source Conference, Philadelphia, PA, 2008 (Army Research Laboratory, 2003), pp. 615–619.
  8. J. Wang, E. Besnoin, A. Duckham, S. J. Spey, M. E. Reiss, O. M. Knio, M. Powers, M. Whitener, and T. P. Weihs, Appl. Phys. Lett. 83, 3987 (2003).
  9. A. Duckham, S. J. Spey, J. Wang, M. E. Reiss, T. P. Weihs, E. Besnoin, and O. M. Knio, J. Appl. Phys. 96, 2336 (2004).
  10. X. Qiu and J. Wang, Sens. Actuators, A A141, 476 (2008).
  11. A. J. Swiston, Jr., E. Besnoin, A. Duckham, O. M. Knio, T. P. Weihs, and T. C. Hufnagel, Acta Mater. 53, 3713 (2005).
  12. J. C. Trenkle, T. P. Weihs, and T. C. Hufnagel, Scr. Mater. 58, 315 (2008).
  13. J. Wang, E. Besnoin, A. Duckham, S. J. Spey, M. E. Reiss, O. M. Knio, and T. P. Weihs, J. Appl. Phys. 95, 248 (2004).
  14. J. Wang, E. Besnoin, O. M. Knio, and T. P. Weihs, Acta Mater. 52, 5265 (2004).
  15. J. Wang, E. Besnoin, O. M. Knio, and T. P. Weihs, J. Appl. Phys. 97, 114307 (2005).
  16. C. Suryanarayana, J. J. Moore, and R. P. Radtke, Adv. Mater. Processes 159, 29 (2001).
  17. A. Duckham, M. Brown, E. Besnoin, D. van Heerden, O. M. Knio, and T. P. Weihs, Ceram. Eng. Sci. Proc. 25, 597 (2004).
  18. A. J. Swiston, T. C. Hufnagel, and T. P. Weihs, Scr. Mater. 48, 1575 (2003).
  19. D. Van Heerden, T. Rude, J. Newson, O. Knio, T. P. Weihs, and D. W. Gallus, Twentieth Annual IEEE Semiconductor Thermal Measurement and Management Symposium Proceedings (IEEE, New York, 2004).
  20. W. J. Buehler, J. V. Gilfrich, and R. C. Wiley, J. Appl. Phys. 34, 1475 (1963).
  21. J. A. Shaw and S. Kyriakides, J. Mech. Phys. Solids 43, 1243 (1995).
  22. A. L. McKelvey and R. O. Ritchie, Metall. Mater. Trans. A 32, 731 (2001).
  23. E. Goo and R. Sinclair, Acta Metall. 33, 1717 (1985).
  24. T. Goryczka and H. Morawiec, J. Alloys Compd. 367, 137 (2004
  25. D. P. Adams, V. C. Hodges, M. M. Bai, E. Jones, M. A. Rodriguez, T. Buchheit, and J. J. Moore, J. Appl. Phys. 104, 043502 (2008).
  26. Cohesion in Metals Transition Metal Alloys, edited by F. R. de Boer and D. G. Pettifor (North-Holland, Amsterdam, 1989), Vol. 1.
  27. K. C. Patil, S. T. Aruna, and T. Mimani, Curr. Opin. Solid State Mater. Sci. 6, 507 (2002).
  28. B. Y. Tay, C. W. Goh, Y. W. Gu, C. S. Lim, M. S. Yong, M. K. Ho, and M. H. Myint, J. Mater. Process. Technol. 202, 359 (2008).
  29. C. L. Yeh and W. Y. Sung, J. Alloys Compd. 376, 79 (2004).
  30. B. Y. Li, L. J. Rong, Y. Y. Li, and V. E. Gjunter, Acta Mater. 48, 3895 (2000).
  31. A. Biswas, Acta Mater. 53, 1415 (2005).
  32. H. C. Yi and J. J. Moore, Scr. Metall. 22, 1889 (1988).
  33. The bilayer thickness is equal to the sum of one Ti layer thickness and one Ni layer thickness.
  34. S. Jayaraman, A. B. Mann, M. Reiss, T. P. Weihs, and O. M. Knio, Combust. Flame 124, 178 (2001).
  35. A. J. Gavens, D. Van Heerden, A. B. Mann, M. E. Reiss, and T. P. Weihs, J. Appl. Phys. 87, 1255 (2000).
  36. S. Jayaraman, A. B. Mann, O. M. Knio, D. Van Heerden, G. Bao, and T. P. Weihs, Proceedings of Symposium B on Phase Transformations and Systems Driven Far From Equilibrium at the Materials Research Society Fall Meeting, Boston, MA, 1997 (Materials Research Society, Warrendale, PA, 1998), pp. 563–568.
  37. R. Armstrong, Combust. Sci. Technol. 71, 155 (1990).
  38. C. E. Wickersham and J. E. Poole, J. Vac. Sci. Technol. A 6, 1699 (1988).
  39. P. J. Kelly and S. F. Tinton, Vacuum 45, 507 (1994).
  40. J. P. McDonald, V. C. Hodges, J. Eric, D. Jones, and D. P. Adams, Appl. Phys. Lett. 94, 034102 (2009).
  41. J. C. Trenkle, J. Wang, T. P. Weihs, and T. C. Hufnagel, Appl. Phys. Lett. 87, 153108 (2005).
  42. G. K. Dey, Acta Mater. 51, 2549 (2003).
  43. We clarify that while the term ignition temperature is used in this discussion to characterize effects of a global anneal, we have not differentiated between whether simultaneous reaction occurs or whether foils are reacted via SHS nucleated at one or more sites.
  44. N. Bertolino, M. Monagheddu, A. Tacca, P. Giuliani, C. Zanotti, and U. A. Tamburini, Intermetallics 11, 41 (2003).
  45. J. J. Moore and H. J. Feng, Prog. Mater. Sci. 39, 243 (1995).
  46. J. J. Moore and H. J. Feng, Prog. Mater. Sci. 39, 275 (1995).
  47. D. P. Adams, M. A. Rodriguez, C. P. Tigges, and P. G. Kotula, J. Mater. Res. 21, 3168 (2006).
  48. The observation that Ni/Ti reacts in vacuum, without an abundance of oxygen present, is also interesting considering previous work by Moore and Feng. This other work reported the “initial oxidation of Ti… subsequently triggered the SHS reaction Ni+Ti=NiTi.” Our study conclusively shows that, at least for vapor-deposited structures having nanometer-scale periodicity, the heat of the intermetallic reaction is sufficient to drive SHS.
  49. The coformation of Ni-rich B19[prime] NiTi and NiTi2 precipitates is inconsistent with prior studies that treat NixTiy for long time at elevated temperature (closer to equilibrium). Specifically, work with slightly Ni-rich compositions (similar to the matrix phase in our study) shows dramatically lower martensite start temperature making austenite more prevalent. [See, e.g., summary by T. Sawaguchi, G. Kaistrater, A. Yawny, M. Wagner, and G. Eggeler,Metall. Mater. Trans. A 34A, 2847 (2003)] Therefore, according to these other studies B19[prime] NiTi should be less prevalent.
  50. A. M. Locci, R. Orru, G. Cao, and Z. A. Munir, Intermetallics 11, 555 (2003).
  51. See EPAPS supplementary material at http://dx.doi.org/10.1063/1.3253591 for a more complete listing of indexed reflections and Miller index notation. [EPAPS]

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