Crystalline-to-plastic phase transitions in molecularly thin n-dotriacontane films adsorbed on solid surfaces
Author(s) -
E. Cisternas,
Tomás P. Corrales,
Valeria del Campo,
Pamela A. Soza,
U. G. Volkmann,
Mengjun Bai,
H. Taub,
F. Y. Hansen
Publication year - 2009
Publication title -
the journal of chemical physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.071
H-Index - 357
eISSN - 1089-7690
pISSN - 0021-9606
DOI - 10.1063/1.3213642
Subject(s) - monolayer , phase transition , materials science , phase (matter) , thin film , crystallite , ellipsometry , perpendicular , adsorption , crystallography , analytical chemistry (journal) , chemical physics , condensed matter physics , chemistry , nanotechnology , organic chemistry , physics , geometry , mathematics , metallurgy
doi:10.1063/1.3213642Crystalline-to-rotator phase transitions have been widely studied in bulk hydrocarbons, in particular in normal alkanes. But few studies of these transitions deal with molecularly thin films of pure n-alkanes on solid substrates. In this work, we were able to grow dotriacontane (n-C32H66) films without coexisting bulk particles, which allows us to isolate the contribution to the ellipsometric signal from a monolayer of molecules oriented with their long axis perpendicular to the SiO2 surface. For these submonolayer films, we found a step in the ellipsometer signal at ∼ 331 K, which we identify with a solid-solid phase transition. At higher coverages, we observed additional steps in the ellipsometric signal that we identify with a solid-solid phase transition in multilayer islands ( ∼ 333 K) and with the transition to the rotator phase in bulk crystallites ( ∼ 337 K), respectively. After considering three alternative explanations, we propose that the step upward in the ellipsometric signal observed at ∼ 331 K on heating the submonolayer film is the signature of a transition from a perpendicular monolayer phase to a denser phase in which the alkane chains contain on average one to two gauche defects per molecule.This work was supported by the Chilean
government through FONDECYT Grant Nos. 1060628 and 7080105 and by CONICYT scholarships (E.A.C., V.d.C. and
P.A.S.), and by the U.S. NSF Grant No. DMR-0705974
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