Order and Melting in Self-Assembled Alkanol Monolayers on Amorphous SiO2

Haddad, J; Steinrueck, HG; Hlaing, H; Kewalramani, S; Pontoni, D; Reichert, H; Murphy, BM; Festersen, S; Runge, B; Magnussen, OM; Magerl, A; Deutsch, M; Ocko, BM

HERO ID

4937186

Reference Type

Journal Article

Year

2015

HERO ID 4937186
In Press No
Year 2015
Title Order and Melting in Self-Assembled Alkanol Monolayers on Amorphous SiO2
Authors Haddad, J; Steinrueck, HG; Hlaing, H; Kewalramani, S; Pontoni, D; Reichert, H; Murphy, BM; Festersen, S; Runge, B; Magnussen, OM; Magerl, A; Deutsch, M; Ocko, BM
Journal Journal of Physical Chemistry C
Volume 119
Issue 31
Page Numbers 17648-17654
Abstract Molecular self-assembly is a key to wide-ranging nano- and microscale applications in numerous fields. Understanding its underlying molecular level science is therefore of prime importance. This study resolves the angstrom-scale structure of the earliest and simplest self-assembled monolayer (SAM), octadecanol on amorphous-SiO2-terminated Si(001) substrate, and determines the structures temperature evolution. At low temperatures lateral hexagonal order exists, with close-packed, surface-normal molecules. At similar to 12 degrees C above the alkanols bulk melting, a fully reversible disordering transition occurs to a novel stretched liquid phase, laterally disordered, but only similar to 15% thinner SAM than in the crystalline phase. The SAM persists to >= 100 degrees C. A thermodynamic model yields here a headgroup-substrate bond energy similar to 40% lower than on crystalline sapphire, highlighting the importance of the substrates order, and near-epitaxy, for the SAMs ordering and stability.
Doi 10.1021/acs.jpcc.5b03554
Wosid WOS:000359332200017
Is Certified Translation No
Dupe Override No
Is Public Yes