Assessing Impacts of Atmospheric Conditions on Efficiency and Siting of Large-Scale Direct Air Capture Facilities.

The cost and efficiency of direct air capture (DAC) of carbon dioxide (CO2) will be decisive in determining whether this technology can play a large role in decarbonization. To probe the role of meteorological conditions on DAC we examine, at 1 × 1° resolution for the continental United States (U.S.), the impacts of temperature, humidity, atmospheric pressure, and CO2 concentration for a representative amine-based adsorption process. Spatial and temporal variations in atmospheric pressure and CO2 concentration lead to strong variations in the CO2 available in ambient air across the U.S. The specific DAC process that we examine is described by a process model that accounts for both temperature and humidity. A process that assumes the same operating choices at all locations in the continental U.S. shows strong variations in performance, with the most influential variables being the H2O gas phase volume fraction and temperature, both of which are negatively correlated with DAC productivity for the specific process that we consider. The process also shows a moderate positive correlation of ambient CO2 with productivity and recovery. We show that optimizing the DAC process at seven representative locations to reflect temporal and spatial variations in ambient conditions significantly improves the process performance and, more importantly, would lead to different choices in the sites for the best performance than models based on a single set of process conditions. Our work provides a framework for assessing spatial variations in DAC performance that could be applied to any DAC process and indicates that these variations will have important implications in optimizing and siting DAC facilities.

Probing Structural Defects in MOFs Using Water Stability.

Defects in the crystal structures of metal-organic frameworks (MOFs), whether present intrinsically or introduced via so-called defect engineering, can play strong roles in the properties of MOFs for various applications. Unfortunately, direct experimental detection and characterization of defects in MOFs are very challenging. We show that in many cases, the differences between experimentally observed and computationally predicted water stabilities of MOFs can be used to deduce information on the presence of point defects in real materials. Most computational studies of MOFs consider these materials to be defect-free, and in many cases, the resulting structures are predicted to be hydrophobic. Systematic experimental studies, however, have shown that many MOFs are hydrophilic. We show that the existence of chemically plausible point defects can often account for this discrepancy and use this observation in combination with detailed molecular simulations to assess the impact of local defects and flexibility in a variety of MOFs for which defects had not been considered previously.

Efficient Generation of Large Collections of Metal-Organic Framework Structures Containing Well-Defined Point Defects.

High-throughput molecular simulations of metal-organic frameworks (MOFs) are a useful complement to experiments to identify candidates for chemical separation and storage. All previous efforts of this kind have used simulations in which MOFs are approximated as defect-free. We introduce a tool to readily generate missing-linker defects in MOFs and demonstrate this tool with a collection of 507 defective MOFs. We introduce the concept of the maximum possible defect concentration; at higher defect concentrations, deviations from the defect-free crystal structure would be readily evident experimentally. We studied the impact of defects on molecular adsorption as a function of defect concentrations. Defects have a slightly negative or negligible influence on adsorption at low pressures for ethene, ethane, and CO2 but a strong positive influence for methanol due to hydrogen bonding with defects. Defective structures tend to have loadings slightly higher than those of defect-free structures for all adsorbates at elevated pressures.