Film Quality and Electronic Properties of a Surface-Anchored Metal-Organic Framework Revealed by using a Multi-technique Approach

The virtually unlimited versatility and unparalleled level of control in the design of metal-organic frameworks (MOFs) has recently been shown to also entail a potential for applications based on the electrical and electronic properties of this rich class of materials. At present, methods to provide...

Descripción completa

Detalles Bibliográficos
Autores: Liu, Jianxi, Paradinas, Markos|||0000-0003-1006-9506, Heinke, Lars, Buck, Manfred, Ocal García, Carmen|||0000-0001-8790-8844, Mugnaini, Veronica|||0000-0002-5633-489X, Wöll, Christof
Tipo de recurso: artículo
Fecha de publicación:2016
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:212919
Acceso en línea:https://ddd.uab.cat/record/212919
https://dx.doi.org/urn:doi:10.1002/celc.201500486
Access Level:acceso abierto
Palabra clave:Cyclic voltammetry
Defect-free film
Ferrocene
Ionic liquids
Metal-organic frameworks
Descripción
Sumario:The virtually unlimited versatility and unparalleled level of control in the design of metal-organic frameworks (MOFs) has recently been shown to also entail a potential for applications based on the electrical and electronic properties of this rich class of materials. At present, methods to provide reliable and reproducible contacts to MOF materials are scarce; therefore, we have carried out a detailed, multi-technique investigation of an empty and loaded prototype MOF, HKUST-1. Epitaxial thin films of this material grown on a substrate by using liquid-phase epitaxy have been studied by cyclic voltammetry, atomic force microscopy, and quartz crystal microbalance and their quality assessed. By using an ionic liquid as the electrolyte, it is shown that redox-active molecules like ferrocene can be embedded in the pores, enabling a change in the overall conductivity of the framework and the study of the redox chemistry of guest molecules inside the MOF.