There is an urgent need for inexpensive, functional materials that can capture and release CO under industrial conditions. In this context, MgO is a highly promising, earth-abundant CO sorbent. However, despite its favorable carbonation thermodynamics and potential for high gravimetric CO uptakes, MgO-based CO sorbents feature slow carbonation kinetics, limiting their CO uptake during typical industrial contact times.
View Article and Find Full Text PDFDue to their high structural tunability, remarkable internal surface areas, readily accessible pore space, and host of possible applications, covalent organic frameworks (COFs) remain at the forefront of materials science research. Unfortunately, many COFs suffer from structural distortions or pore collapse during activation, which can lead to a substantial loss of crystallinity and functionality. Thus, herein, we demonstrate a facile method to address this issue by introducing polymer guests.
View Article and Find Full Text PDFGrowing polymers inside porous metal-organic frameworks (MOFs) can allow incoming guests to access the backbone of otherwise non-porous polymers, boosting the number and/or strength of available adsorption sites inside the porous support. In the present work, we have devised a novel post-synthetic modification (PSM) strategy that allows one to graft metal-chelating functionality onto a polymer backbone while inside MOF pores, enhancing the material's ability to recover Pt(iv) from complex liquids. For this, polydopamine (PDA) was first grown inside of a MOF, known as Fe-BTC (or MIL-100 Fe).
View Article and Find Full Text PDFMetal-organic frameworks (MOFs) are a rapidly growing class of materials that offer great promise in various applications. However, the synthesis remains challenging: for example, a range of crystal structures can often be accessed from the same building blocks, which complicates the phase selectivity. Likewise, the high sensitivity to slight changes in synthesis conditions may cause reproducibility issues.
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