Positional order and thermal expansion of surface crystalline N-alkane monolayers

B. M. Ocko, E. B. Sirota, M. Deutsch, E. DiMasi, S. Coburn, Joe Strzalka, Songyan Zheng, Andrey Tronin, Thomas Gog, and Chitra Venkataraman
Phys. Rev. E 63, 032602 – Published 27 February 2001
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Abstract

We report a high-resolution synchrotron grazing incidence x-ray diffraction measurement of a surface crystalline monolayer at the liquid-vapor interface of the n-alkane eicosane (C20H42) just above its melting temperature. The peak width of the surface monolayer rotator phase is shown to be resolution limited and implies positional correlations of at least ∼1 μm. The high resolution allowed determination of the temperature dependence of the peak position over the narrow (3 °C) temperature range of the surface crystal phase. The two-dimensional thermal expansion was determined to be (dA/dT)/A=1.8(±0.1)×103°C1, which is comparable to the expansion in similar chain length bulk n-alkane rotator phases. Our data are consistent with the power-law shaped scattering tails expected from quasi-long-range order in two dimensions.

  • Received 10 October 2000

DOI:https://doi.org/10.1103/PhysRevE.63.032602

©2001 American Physical Society

Authors & Affiliations

B. M. Ocko1, E. B. Sirota2, M. Deutsch3, E. DiMasi1, S. Coburn1, Joe Strzalka4, Songyan Zheng4, Andrey Tronin4, Thomas Gog5, and Chitra Venkataraman5

  • 1Physics Department, Brookhaven National Laboratory, Upton, New York 11973
  • 2ExxonMobil Research and Engineering Company, Route 22 East, Annandale, New Jersey 08801
  • 3Department of Physics, Bar Ilan University, Ramat Gan 52900, Israel
  • 4Department of Chemistry, University of Pennsylvania, Philadelphia, Pennsylvania 19104
  • 5Complex Materials Consortium, Collaborative Access Team, Advanced Photon Source, Argonne National Laboratory, Argonne, Illinois 60439

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Vol. 63, Iss. 3 — March 2001

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