Abstract Carbon capture and sequestration (CCS) from industrial point sources and direct air capture are necessary to combat global climate change. A particular challenge faced by amine‐based sorbents—the current leading technology—is poor stability towards O2. Here, we demonstrate that CO2chemisorption in γ‐cylodextrin‐based metal–organic frameworks (CD‐MOFs) occurs via HCO3−formation at nucleophilic OH−sites within the framework pores, rather than via previously proposed pathways. The new framework KHCO3CD‐MOF possesses rapid and high‐capacity CO2uptake, good thermal, oxidative, and cycling stabilities, and selective CO2capture under mixed gas conditions. Because of its low cost and performance under realistic conditions, KHCO3CD‐MOF is a promising new platform for CCS. More broadly, our work demonstrates that the encapsulation of reactive OH−sites within a porous framework represents a potentially general strategy for the design of oxidation‐resistant adsorbents for CO2capture.
more »
« less
Carbon Capture Beyond Amines: CO 2 Sorption at Nucleophilic Oxygen Sites in Materials
Abstract Carbon capture and utilization or sequestration and direct air capture will be needed to reduce atmospheric levels of greenhouse gases over the next century. Current amine‐based technologies bind CO2with high selectivities but suffer from poor oxidative and thermal stabilities. Herein, we discuss understudied sorbents based on oxygen nucleophiles, including metal oxides and hydroxides, hydroxide‐containing polymers, and hydroxide‐based metal–organic frameworks. In general, these materials display improved oxidative stabilities compared to traditional amine‐based sorbents. We outline the challenges and opportunities offered by these alternative sorbents for carbon capture applications.
more »
« less
- Award ID(s):
- 2047627
- PAR ID:
- 10379725
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- ChemNanoMat
- Volume:
- 9
- Issue:
- 1
- ISSN:
- 2199-692X
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
-
Abstract Carbon dioxide capture technologies are set to play a vital role in mitigating the current climate crisis. Solid‐state17O NMR spectroscopy can provide key mechanistic insights that are crucial to effective sorbent development. In this work, we present the fundamental aspects and complexities for the study of hydroxide‐based CO2capture systems by17O NMR. We perform static density functional theory (DFT) NMR calculations to assign peaks for general hydroxide CO2capture products, finding that17O NMR can readily distinguish bicarbonate, carbonate and water species. However, in application to CO2binding in two test case hydroxide‐functionalised metal‐organic frameworks (MOFs) – MFU‐4l and KHCO3‐cyclodextrin‐MOF, we find that a dynamic treatment is necessary to obtain agreement between computational and experimental spectra. We therefore introduce a workflow that leverages machine‐learning force fields to capture dynamics across multiple chemical exchange regimes, providing a significant improvement on static DFT predictions. In MFU‐4l, we parameterise a two‐component dynamic motion of the bicarbonate motif involving a rapid carbonyl seesaw motion and intermediate hydroxyl proton hopping. For KHCO3‐CD‐MOF, we combined experimental and modelling approaches to propose a new mixed carbonate‐bicarbonate binding mechanism and thus, we open new avenues for the study and modelling of hydroxide‐based CO2capture materials by17O NMR.more » « less
-
Abstract Rising anthropogenic carbon emissions have dire environmental consequences, necessitating remediative approaches, which includes use of solid sorbents. Here, aminopolymers (poly(ethylene imine) (PEI) and poly(propylene imine) (PPI)) are supported within solid mesoporous MIL‐101(Cr) to examine effects of support defect density on aminopolymer‐MOF interactions for CO2uptake and stability during uptake‐regeneration cycles. Using simulated flue gas (10 % CO2in He), MIL‐101(Cr)‐ρhigh(higher defect density) shows 33 % higher uptake capacity per gram adsorbent than MIL‐101(Cr)‐ρlow(lower defect density) at 308 K, consistent with increased availability of undercoordinated Cr adsorption sites at missing linker defects. Increasing aminopolymer weight loadings (10–50 wt.%) within MIL‐101(Cr)‐ρlowand MIL‐101(Cr)‐ρhighincreases amine efficiencies and CO2uptake capacities relative to bare MOFs, though both incur CO2diffusion limitations through confined, viscous polymer phases at higher (40–50 wt.%) loadings. Benchmarked against SBA‐15, lower polymer packing densities (PPI>PEI), weaker and less abundant van der Waals interactions between aminopolymers and pore walls, and open framework topology increase amine efficiencies. Interactions between amines and Cr defect sites incur amine efficiency losses but grant higher thermal and oxidative stability during uptake‐regeneration cycling. Finally, >25 % higher CO2uptake capacities are achieved for aminopolymer/MIL‐101(Cr)‐ρhighunder humid conditions, demonstrating promise for realistic applications.more » « less
-
Abstract The capture, utilization, and storage of CO2are the primary options to minimize the adverse effects of global warming and related climate change resulting from increased anthropogenic CO2emissions. In recent years, amino acids and amino acid‐based ionic liquids (AAILs) are proposed as promising alternatives to the traditional aqueous amine solvent‐based CO2capture technology due to the presence of the ─NH2group and a CO2adsorption mechanism like amines, but with many additional advantages. Besides CO2absorption in solvent form, amino acids/AAILs‐functionalized porous sorbents demonstrate potential in CO2adsorption technology, a promising alternative to solvent‐based CO2absorption technology, as they can avoid the huge energy penalty associated with aqueous solution regeneration by heating. Additionally, amino acids/AAILs, with their CO2capture abilities, have demonstrated their potential in other promising CO2sequestration technologies: direct air capture, CO2mineralization using alkaline industrial waste, and conversion of CO2into value‐added products. This article reviews the mechanism, comparative performance, and prospects of amino acid‐based state‐of‐the‐art technologies for CO2absorption and adsorption, direct air capture, bio‐mineralization, and conversion of CO2into value‐added products, which is helpful for the further development of amino acid‐based CO2sequestration technologies.more » « less
-
Given the continuous and excessive CO 2 emission into the atmosphere from anthropomorphic activities, there is now a growing demand for negative carbon emission technologies, which requires efficient capture and conversion of CO 2 to value-added chemicals. This review highlights recent advances in CO 2 capture and conversion chemistry and processes. It first summarizes various adsorbent materials that have been developed for CO 2 capture, including hydroxide-, amine-, and metal organic framework-based adsorbents. It then reviews recent efforts devoted to two types of CO 2 conversion reaction: thermochemical CO 2 hydrogenation and electrochemical CO 2 reduction. While thermal hydrogenation reactions are often accomplished in the presence of H 2 , electrochemical reactions are realized by direct use of electricity that can be renewably generated from solar and wind power. The key to the success of these reactions is to develop efficient catalysts and to rationally engineer the catalyst–electrolyte interfaces. The review further covers recent studies in integrating CO 2 capture and conversion processes so that energy efficiency for the overall CO 2 capture and conversion can be optimized. Lastly, the review briefs some new approaches and future directions of coupling direct air capture and CO 2 conversion technologies as solutions to negative carbon emission and energy sustainability.more » « less
An official website of the United States government
