Lehrstuhl für Physikalische Chemie II, Friedrich-Alexander-Universität Erlangen-Nürnberg, Egerlandstrasse 3, 91058, Erlangen, Germany.
Instituto de Desarrollo Tecnológico para la Industria Química (INTEC) UNL-CONICET, Güemes 3450, 3000, Santa Fe, Argentina.
Angew Chem Int Ed Engl. 2017 Jul 24;56(31):9072-9076. doi: 10.1002/anie.201704107. Epub 2017 Jun 28.
Ionic liquids (IL) hold a great potential as novel electrolytes for applications in electronic materials and energy technology. The functionality of ILs in these applications relies on their interface to semiconducting nanomaterials. Therefore, methods to control the chemistry and structure of this interface are the key to assemble new IL-based electronic and electrochemical materials. Here, we present a new method to prepare a chemically well-defined interface between an oxide and an IL film. An imidazolium-based IL, which is carrying an ester group, is deposited onto cobalt oxide surface by evaporation. The IL binds covalently to the surface by thermally activated cleavage of the ester group and formation of a bridging carboxylate. The anchoring reaction shows high structure sensitivity, which implies that the IL film can be adhered selectively to specific oxide surfaces.
离子液体(IL)作为新型电解质在电子材料和能源技术中有很大的应用潜力。在这些应用中,IL 的功能取决于它们与半导体纳米材料的界面。因此,控制这种界面化学和结构的方法是组装新型基于 IL 的电子和电化学材料的关键。在这里,我们提出了一种在氧化物和 IL 薄膜之间制备化学定义明确界面的新方法。通过蒸发将一种带有酯基的咪唑基 IL 沉积到氧化钴表面上。通过酯基的热激活裂解和桥接羧酸根的形成,IL 与表面发生共价键合。锚固反应表现出很高的结构敏感性,这意味着 IL 薄膜可以选择性地附着在特定的氧化物表面上。