Probing Structural Transformations and Degradation Mechanisms by Direct Observation in SIFSIX-3-Ni for Direct Air Capture.

Despite global efforts to reduce carbon dioxide (CO2) emissions, continued industrialization threatens to exacerbate climate change. This work investigates methods to capture CO2, with a focus on the SIFSIX-3-Ni metal-organic framework (MOF) as a direct air capture (DAC) sorbent. SIFSIX-3-Ni exhibits promising CO2 adsorption properties but suffers from degradation processes under accelerated aging, which are akin to column regeneration conditions. Herein, we have grown the largest SIFSIX-3-Ni single crystals to date, facilitating single crystal X-ray diffraction analyses that enabled direct observation of the H2O and CO2 dynamics through adsorption and desorption. In addition, a novel space group (I4/mcm) for the SIFSIX-3-Ni is identified, which provided insights into structural transitions within the framework and elucidated water's role in degrading CO2 uptake performance as the material ages. In situ X-ray scattering methods revealed long-range and local structural transformations associated with CO2 adsorption in the framework pores as well as a temperature-dependent desorption mechanism. Pair distribution function analysis revealed a partial decomposition to form nonporous single-layer nanosheets of edge-sharing nickel oxide octahedra upon aging. The formation of these nanosheets is irreversible and reduces the amount of active material for the CO2 sorption. These findings provide crucial insights for the development of efficient and stable DAC sorbents, effectively reducing greenhouse gases, and suggest avenues for enhancing MOF stability under practical DAC conditions.

Expanding the Library of Ions for Moisture-Swing Carbon Capture.

Developing materials that can more efficiently and cheaply capture carbon dioxide from ambient atmospheric conditions is essential for improving negative emission technologies. This study builds on the promising moisture-swing modality for direct air capture of carbon dioxide by investigating the use of several new anions─orthosilicate, borate, pyrophosphate, tripolyphosphate, and dibasic phosphate─that when introduced into ion-exchange resins allow for the cyclable capture of CO2 under dry conditions and its release under wet conditions. These ions, as well as many others that failed to show moisture-swing performance, are tested and directly compared thermodynamically and kinetically to understand their differences. This includes the use of analytical approaches new to the carbon capture field, such as the correlation of adsorption isotherms to moisture-swing performance, the use of phase lag kinetics, the examination of the humidity-carbon capture hysteresis of the sorbents, and the precise quantification of ion loading using inductively coupled plasma-optical emission spectroscopy. Phosphate dibasic was found to have the largest mass-normalized CO2 moisture-swing capacity, whereas phosphate tribasic had the best performance when factoring in kinetics, and pyrophosphate had the highest swing capacity when normalizing on a per-ion or per-unit-charge basis. This work not only sheds light on ways to improve DAC but also provides insights pertinent to the advancement of gas separation, negative emission technologies, and sorbent materials.

Suitability of a diamine functionalized metal-organic framework for direct air capture.

The increase in the atmospheric carbon dioxide level is a significant threat to our planet, and therefore the selective removal of CO2 from the air is a global concern. Metal-organic frameworks (MOFs) are a class of porous materials that have shown exciting potential as adsorbents for CO2 capture due to their high surface area and tunable properties. Among several implemented technologies, direct air capture (DAC) using MOFs is a promising strategy for achieving climate targets as it has the potential to actively reduce the atmospheric CO2 concentration to a safer levels. In this study, we investigate the stability and regeneration conditions of N,N'-dimethylethylenediamine (mmen) appended Mg2(dobpdc), a MOF with exceptional CO2 adsorption capacity from atmospheric air. We employed a series of systematic experiments including thermogravimetric analysis (TGA) coupled with Fourier transformed infrared (FTIR) and gas chromatography mass spectrometer (GCMS) (known as TGA-FTIR-GCMS), regeneration cycles at different conditions, control and accelerated aging experiments. We also quantified CO2 and H2O adsorption under humid CO2 using a combination of data from TGA-GCMS and coulometric Karl-Fischer titration techniques. The quantification of CO2 and H2O adsorption under humid conditions provides vital information for the design of real-world DAC systems. Our results demonstrate the stability and regeneration conditions of mmen appended Mg2(dobpdc). It is stable up to 50% relative humidity when the adsorption temperature varies from 25-40 °C and the best regeneration condition can be achieved at 120 °C under dynamic vacuum and at 150 °C under N2.