Wearable electronics have the potential to advance personalized health care, alleviate disability, enhance communication, and improve homeland security. Development of multifunctional electronic textiles (e-textiles) with the capacity to interact with the local environment is a promising strategy for achieving electronic transduction of physical and chemical information. This paper describes a simple and rapid approach for fabricating multifunctional e-textiles by integrating conductive two-dimensional (2D) metal-organic frameworks (MOFs) into fabrics through direct solution-phase self-assembly from simple molecular building blocks. These e-textiles display reliable conductivity, enhanced porosity, flexibility, and stability to washing. The functional utility of these integrated systems is demonstrated in the context of chemiresistive gas sensing, uptake, and filtration. The self-organized frameworks on textiles (SOFT)-devices detect and differentiate important gaseous analytes (NO, HS, and HO) at ppm levels and maintain their chemiresistive function in the presence of humidity (5000 ppm, 18% RH). With sub-ppm theoretical limits of detection (LOD for NO = 0.16 ppm and for HS = 0.23 ppm), these constitute the best textile-supported HS and NO detectors reported and the best MOF-based chemiresistive sensors for these analytes. In addition to sensing, these devices are capable of capturing and filtering analytes.
The synthetically tunable properties and intrinsic porosity of conductive metal-organic frameworks (MOFs) make them promising materials for transducing selective interactions with gaseous analytes in an electrically addressable platform. Consequently, conductive MOFs are valuable functional materials with high potential utility in chemical detection. The implementation of these materials, however, is limited by the available methods for device incorporation due to their poor solubility and moderate electrical conductivity. This manuscript describes a straightforward method for the integration of moderately conductive MOFs into chemiresistive sensors by mechanical abrasion. To improve electrical contacts, blends of MOFs with graphite were generated using a solvent-free ball-milling procedure. While most bulk powders of pure conductive MOFs were difficult to integrate into devices directly via mechanical abrasion, the compressed solid-state MOF/graphite blends were easily abraded onto the surface of paper substrates equipped with gold electrodes to generate functional sensors. This method was used to prepare an array of chemiresistors, from four conductive MOFs, capable of detecting and differentiating NH3, H2S and NO at parts-per-million concentrations.
The
vibrational characteristics of 28 different boronic acid, boroxine
anhydride, and boronate ester species have been systematically investigated
using a combination of experimental infrared (IR) spectroscopy and
computational modeling. IR bands characteristic to each boron-containing
functionality have been categorized and assigned in conjunction with
density functional theory (B3LYP/6-31G(d)), with the aim of better
understanding and distinguishing the vibrational characteristics of
covalent organic frameworks (COFs) built from boronic acids. In several
cases, vibrational assignments differ from those previously reported
in the literature on boronic acid-based COFs. Vibrations commonly
regarded as diagnostic for one functionality are found in regions
of the IR spectrum where other functionalities also show characteristic
peaks. The collective experimental and computational results reveal
that several alternative bands in the IR region can be used to more
diagnostically distinguish between boronic acid, boroxine anhydride,
and boronate ester species. The results presented herein provide the
tools for straightforward characterization of boroxine anhydride and
boronate ester species using IR spectroscopy. The results can be applied
to additional theoretical studies of larger COF-like assemblies as
well as the analysis of other boronic-acid-based materials.
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