Meltzer Christian, Dietrich Hanno, Zahn Dirk, Peukert Wolfgang, Braunschweig Björn
†Institute of Particle Technology (LFG), ‡Erlangen Graduate School in Advanced Optical Technologies (SAOT), §Computer-Chemie-Centrum and Interdisciplinary Center for Molecular Materials, ∥Chair of Theoretical Chemistry, and ⊥Cluster of Excellence - Engineering of Advanced Materials (EAM), Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), 91058 Erlangen, Germany.
Langmuir. 2015 Apr 28;31(16):4678-85. doi: 10.1021/acs.langmuir.5b00440. Epub 2015 Apr 14.
The growth of self-assembled monolayers (SAMs) of octadecylphosphonic acid (ODPA) molecules on α-Al2O3(0001) and subsequent dewetting of the SAMs were studied with a combination of in situ sum-frequency generation (SFG) and molecular dynamics (MD) simulations. Although SAM growth after deposition times >8 h reduces to nearly negligible values, the resultant ODPA SAMs in solution are still not in a well-ordered state with the alkyl chains in all-trans configurations. In fact, in situ SFG spectroscopy revealed a comparatively high concentration of gauche defects of the SAM in the ODPA 2-propanol solution even after a growth time of 16 h. Here, results of the MD simulations strongly suggest that defects can be caused by ODPA molecules which are not attached to the substrate but are incorporated into the SAM layer with the polar headgroup oriented into the 2-propanol solvent. This inverted adsorption geometry of additional ODPA molecules blocks adsorption sites and thus stabilizes the SAM without improving ordering to an extent that all molecules are in the all-trans configuration. While persistent in solution, the observed defects can be healed out when the SAMs are transferred from the solvent to a gas phase. During this process, a quasi-Langmuir-Blodgett transfer of molecules takes place which drives the SAM into a higher conformational state and significantly improves its quality.
采用原位和频产生(SFG)与分子动力学(MD)模拟相结合的方法,研究了十八烷基膦酸(ODPA)分子在α-Al2O3(0001)上自组装单分子层(SAMs)的生长以及随后SAMs的去湿过程。尽管沉积时间>8小时后SAM的生长速率降低到几乎可以忽略不计的值,但所得ODPA SAMs在溶液中仍未处于烷基链全反式构型的有序状态。事实上,原位SFG光谱显示,即使在生长16小时后,ODPA异丙醇溶液中SAM的gauche缺陷浓度相对较高。在此,MD模拟结果强烈表明,缺陷可能是由未附着在基底上但以极性头基团朝向异丙醇溶剂的方式掺入SAM层的ODPA分子引起的。额外ODPA分子的这种反向吸附几何结构会阻塞吸附位点,从而稳定SAM,但不会将有序度提高到所有分子都处于全反式构型的程度。虽然在溶液中缺陷持续存在,但当SAM从溶剂转移到气相时,观察到的缺陷可以消除。在此过程中,分子发生准朗缪尔-布洛杰特转移,这会使SAM进入更高的构象状态并显著提高其质量。