Abstract

Metal-organic frameworks (MOFs) are extremely porous, crystalline materials with high surface area for potential use in gas storage, sequestration, and separations. Toward incorporation into structures for these applications, this study compares three variations of surface-bound and free-standing HKUST-1 MOF structures: surface-anchored MOF (surMOF) thin film, drop-cast film, and bulk powder. Herein, effects of HKUST-1 ammonia interaction and framework activation, which is removal of guest molecules via heat, are investigated. Impact on morphology and crystal structure as a function of surface confinement and size variance are examined. Scanning probe microscopy, scanning electron microscopy, powder X-ray diffraction, Fourier-transform infrared spectroscopy, and energy dispersive X-ray spectroscopy monitor changes in morphology and crystal structure, track ammonia uptake, and examine elemental composition. After fabrication, ammonia uptake is observed for all MOF variations, but reveals dramatic morphological and crystal structure changes. However, activation of the framework was found to stabilize morphology. For activated surMOF films, findings demonstrate consistent morphology throughout uptake, removal, and recycling of ammonia over multiple exposures. To understand morphological effects, additional ammonia exposure experiments with controlled post-synthetic solvent adsorbates were conducted utilizing a HKUST-1 standard powder. These findings are foundational for determining the capabilities and limitation of MOF films and powders.

Highlights

  • Porous crystalline materials known as metal-organic frameworks (MOFs) have been the focus of much attention over recent years due to their promising potential for a wide range of applications, including gas storage, separation, catalysis, and sensing [1,2,3]

  • To investigate how ammonia interacts with the HKUST-1 metal-organic framework, three different variations of the material were exposed to ammonia; and the effect was monitored via microscopy, Infrared Spectroscopy (IR), and powder X-ray diffraction (XRD)

  • The scanning probe microscopy (SPM) characterization was undertaken to monitor how ammonia interacts with the surface-anchored MOF (surMOF) deposited by a layer-by-layer protocol onto a gold surface functionalized with a self-assembled monolayer

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Summary

Introduction

Porous crystalline materials known as metal-organic frameworks (MOFs) have been the focus of much attention over recent years due to their promising potential for a wide range of applications, including gas storage, separation, catalysis, and sensing [1,2,3]. Careful selection of the inorganic nodes and organic linkers that compose the chemical structure of the material can lead to a variety of highly tunable pore sizes and chemical functionality [4]. Varying synthetic conditions, such as processing solvent [5], temperature [6], concentration [7], etc., allows one to tailor MOF properties. This careful control makes it possible to embed MOF materials within an array of hierarchical architectures and composites [8]. When testing the materials in the presence of Nanomaterials 2018, 8, 650; doi:10.3390/nano8090650 www.mdpi.com/journal/nanomaterials

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