ABSTRACT
The coverage dependent phase behavior of monolayers of alkyl thiols (CH3(CH2)(n-1)SH, denoted as CnSH) on mercury was studied for chain lengths 9
ABSTRACT
The structure of octadecanethiol monolyers on liquid Hg surfaces, measured with subangstrom resolution, evolves with increasing coverage from a laterally disordered phase of surface-parallel molecules to ordered rotator phases of surface-normal molecules. For the latter, an abrupt transition is found at 19 A(2)/molecule from a rectangular packing of molecules tilted by 27 degrees in the nearest-neighbor direction to a hexagonal unit cell of untilted molecules. The unit cell of the tilted phase is centered for the chains and noncentered for the headgroups. The thiol headgroups associate in pairs with a single Hg atom, and the bonds form long-range orientational order. The different order of thiols on Au(111) and on Hg highlights the subphase's role in determining the overlayer's structure.
ABSTRACT
The temperature dependent phase behavior of Langmuir films of n-alkanes [CH3(CH2)(n-2)CH3, denote Cn] on mercury was studied for chain lengths 19< or =n< or =22 and temperatures 15< or =T< or =44 degrees C, using surface tensiometry and surface x-ray diffraction methods. In contrast with Langmuir films on water, where molecules invariably orient roughly surface normal, alkanes on mercury are always oriented surface parallel and show no long-range in-plane order at any surface pressure. A gas and several condensed phases of single, double, and triple layers of lying-down molecules are found, depending on n and T. At high coverages, the alkanes studied here show transitions from a triple to a double to a single layer with increasing temperature. The transition temperature from a double to a single layer is found to be approximately 5 degrees C, lower than the bulk rotator-to-liquid melting temperature, while the transition from a triple to a double layer is about as much below the double-to-single layer transition. Both monolayer and bulk transition temperatures show a linear increase with n with identical slopes of approximately 4.5 degrees C/CH2 within the range of n values addressed here. It is suggested that the film and bulk transitions are both driven by a common cause: the proliferation of gauche defects in the chain with increasing temperature.
Subject(s)
Alkanes/chemistry , Mercury/chemistry , Phase Transition , Surface Properties , Thermodynamics , Transition Temperature , X-Ray DiffractionABSTRACT
The structure and phase behavior of liquid-mercury-supported molecular films of fatty acids (CH3(CH2)n-2COOH, denoted CnOOH) were studied for molecular lengths 7 < or = n < or = 24, by surface tensiometry and X-ray methods. Two qualitatively different film structures were found, depending on coverage. For high coverage, the film consists of a monolayer of roughly surface-normal molecules, showing a pressure-dependent sequence of structures similar, though not identical, to that of the corresponding water-supported Langmuir films. At low coverage, phases consisting of surface-parallel molecules are found, not observed on the aqueous subphases employed to date. In this range, a two-dimensional (2D) gas followed by a single and, for 14 < or = n < or = 24, also by a double layer of surface-parallel molecules is found as coverage is increased. Depending on chain length, the flat-lying phases have a crystalline 2D-ordered, a smectic-like 1D-ordered, or a disordered in-plane structure consisting of molecular dimers. The structure and thermodynamics of the films are discussed.
Subject(s)
Fatty Acids/chemistry , Mercury/chemistry , Phase Transition , Pressure , Surface Tension , Thermodynamics , Water/chemistry , X-RaysABSTRACT
The coverage-dependent phase behavior of molecular films of alcohols (CH3(CH2)n-2CH2OH, denoted as CnOH) on mercury was studied for chain lengths 8 < or = n < or = 28, using surface tensiometry and surface specific X-ray methods. Phases with surface-normal-oriented molecules are found at high coverage, showing the CS, S, and LS phases found also on water. Phases comprising surface parallel molecules, which do not exist on water, are found here at low coverage. For the lowest coverage a two-dimensional gas phase is found, followed, upon increasing the coverage, by an n-dependent sequence of condensed phases of up to four layers of surface-parallel molecules before converting to the surface-normal phases. In contrast with the surface-normal phases, all of the surface-parallel phases are found to lack long-range order in the surface-parallel direction. Adsorption energies are derived from the phase diagram for the alkyl chain and the alcohol headgroup.
Subject(s)
Alcohols/chemistry , Mercury/chemistry , Adsorption , Phase Transition , Surface Tension , Temperature , X-RaysABSTRACT
Surface freezing is studied in dry and hydrated alcohol mixtures by surface x-ray scattering and surface tension measurements. A crystalline bilayer is formed at the surface a few degrees above the bulk freezing temperature. The packing is hexagonal, with molecules aligned along the surface normal in all cases. The in-plane lattice constant reveals a qualitatively different behavior with composition for hydrated and dry mixtures. The simple theoretical approach used successfully for alkane and deuterated alkane mixtures accounts well also for the alcohol mixtures. The repulsive length-mismatch term opposing the mixing entropy term in the free energy of the mixtures is shown to have a universal behavior for all mixtures studied: protonated alkanes, deuterated alkanes, and dry and wet alcohols. This universality is somewhat counterintuitive in view of the different interactions (e.g., hydrogen bonding in alcohols) in the different mixtures.
ABSTRACT
The structure of organic monolayers on liquid surfaces depends sensitively on the details of the molecular interactions. The structure of a stearic acid film on a mercury surface was measured as a function of coverage with angstrom resolution. Unlike monolayers on water, the molecules were found here to undergo a transition from surface-parallel to surface-normal orientation with increasing coverage. At high coverage, two condensed hexatic phases of standing-up molecules were found. At low coverage, a two-dimensional (2D) gas phase and condensed single- and double-layered phases of flat-lying molecular dimers were revealed, exhibiting a 1D longitudinal positional order. This system should provide a broader tunability range for nanostructure construction than solid-supported self-assembled monolayers.
ABSTRACT
A thin/thick transition was observed by x-ray reflectivity in a surface-frozen crystalline bilayer on the surface of a molten binary mixture of long alcohols. This rare example of a solid-solid phase transition in a quasi-2D system is shown to result from an abrupt temperature-driven change in the layer's composition, kinetically enabled by the layer's ability to exchange molecules with the underlying 3D liquid bulk. Mean-field thermodynamics yields a Gibbs-adsorption-like expression which accounts very well for the transition.
ABSTRACT
Surface freezing (SF) was investigated in tricosane-dodecane alkane solutions as a function of temperature (T) and molar concentration of tricosane (phi), using surface tension and synchrotron x-ray surface diffraction techniques. A crystalline SF monolayer, having a rotator R(II) structure, was found to exist for 35 degrees C=T=50 degrees C and 0.3=phi=1. The extended temperature range allowed to determine the linear-expansion coefficient of the SF monolayer, (dd/dT)/d=6.5 x 10(-4) degrees C-1. A simple thermodynamical model based on the theory of ideal solutions is shown to account well for the phi dependence of the SF temperature T(s)(phi). The study shows that the temperature range of existence of the surface frozen layer at each phi, the phi range over which SF is observed, and the bulk solidification behavior, are intimately related. All are determined by the rotator-liquid dissolution line T(dR)(phi).