Publications by authors named "M S Barsoum"

This perspective highlights the transformative potential of Metal-Organic Frameworks (MOFs) in environmental and healthcare sectors. It discusses work that has advanced beyond technology readiness levels of >4 including applications in capture, storage, and conversion of gases to value added products. This work showcases efforts in the most salient applications of MOFs which have been performed at a great cadence, enabled by the federal government, large companies, and startups to commercialize these technologies despite facing significant challenges.

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The optimization of nonradiative recombination losses through interface engineering is key to the development of efficient, stable, and hysteresis-free perovskite solar cells (PSCs). In this study, for the first time in solar cell technology, we present a novel approach to interface modification by employing one-dimensional lepidocrocite (henceforth referred to as 1DL) TiO-based nanofilaments, NFs, between the mesoporous TiO (mp TiO) and halide perovskite film in PSCs to improve both the efficiency and stability of the devices. The 1DLs can be easily produced on the kilogram scale starting with cheap and earth-abundant precursor powders, such as TiC, TiN, TiB, etc.

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An innovative process to multifunctional vitrimer nanocomposites with a percolative MXene minor phase is reported, marking a significant advancement in creating stimuli-repairable, reinforced, sustainable, and conductive nanocomposites at diminished loadings. This achievement arises from a Voronoi-inspired biphasic morphological design via a straight-forward three-step process involving ambient-condition precipitation polymerization of micron-sized prepolymer powders, aqueous powder-coating with 2D MXene (TiCT), and melt-pressing of MXene-coated powders into crosslinked films. Due to the formation of MXene-rich boundaries between thiourethane vitrimer domains in a pervasive low-volume fraction conductive network, a low percolation threshold (≈0.

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Electrochemical CO reduction reaction (CO-RR) in non-aqueous electrolytes offers significant advantages over aqueous systems, as it boosts CO solubility and limits the formation of HCO and CO anions. Metal-organic frameworks (MOFs) in non-aqueous CO-RR makes an attractive system for CO capture and conversion. However, the predominantly organic composition of MOFs limits their electrical conductivity and stability in electrocatalysis, where they suffer from electrolytic decomposition.

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