Abstract
A total of 5-30 monolayer thick films of the ionic liquid (IL) [C2C1Im][OTf] were vaporized in vacuo onto an atomically clean Pd(111) single crystal surface at 220 K. Time- and temperature-resolved infrared reflection-absorption spectroscopy reveals growth, interactions with the metallic support, and the macroscopic phase behavior of the layer. At 220 K, the IL layer first grows in the form of a glassy phase. Crystallization of the IL was witnessed above a critical thickness of about 10 monolayers. On the basis of the known bulk crystal structure of the IL, we suggest the formation of well-oriented checkerboard-like crystalline film structures on the surface. The preferential orientation manifested by the crystal phase with regard to the macroscopic metallic surface is attributed to strong interactions between anionic headgroups and the metal.
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