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Title: Preferred orientations and stability of medium length n-alkanes solidified in mesoporous silicon

Journal Article · · Physical Review. E, Statistical Physics, Plasmas, Fluids, and Related Interdisciplinary Topics
; ; ;  [1]
  1. Technische Physik, Universitaet des Saarlandes, D-66041 Saarbruecken (Germany)

The n-alkanes C{sub 16}H{sub 34}, C{sub 17}H{sub 36}, C{sub 19}H{sub 40}, and C{sub 25}H{sub 52} have been imbibed and solidified in mesoporous, crystalline silicon with a mean pore diameter of 10 nm. The structures and phase sequences have been determined by x-ray diffractometry. Apart from a reduction and the hysteresis of the melting-freezing transition, we find a set of six discrete orientation states (''domains'') of the confined alkane crystals with respect to the lattice of the silicon host. The growth process responsible for the domain selection is interpreted as a nanoscale version of the Bridgman technique known from single-crystal growth. Oxidation of the pore walls leads to extrusion of the hydrocarbons upon crystallization, whereas the solidified n-alkanes investigated in nonoxidized, porous silicon are thermodynamically stable.

OSTI ID:
21072377
Journal Information:
Physical Review. E, Statistical Physics, Plasmas, Fluids, and Related Interdisciplinary Topics, Vol. 75, Issue 2; Other Information: DOI: 10.1103/PhysRevE.75.021607; (c) 2007 The American Physical Society; Country of input: International Atomic Energy Agency (IAEA); ISSN 1063-651X
Country of Publication:
United States
Language:
English

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