Investigating the impact of pore structure and surface chemistry on CO2 adsorption in graphitic slit-pores using GCMC simulation

Abstract

Carbon capture, storage, and utilization from post-combustion processes using adsorption phenomena has emerged as a promising solution to the greenhouse gas emission crisis. The capacity of solid porous adsorbents dictates the performance of such carbon capture processes. Developments of porous adsorbents with favourable structural and chemical characteristics of the pore have been a major research area. Computational tools, notably the Grand Canonical Monte Carlo (GCMC) simulation, are widely employed to characterize the adsorption process in crystalline adsorbents like metal-organic frameworks and zeolites. Activated carbons are becoming promising alternatives to conventionally-used zeolite adsorbents for CO2 adsorption, because of their abundant microporosity and cost performance. However, the amorphous nature of the activated carbon materials poses a challenge in accurately modelling their pore characteristics and their adsorption process. Therefore, this study systematically explores the effect of pore size distribution and type of functional groups on the adsorption of CO2 on activated carbons using a simplified slit-pore graphite structure representing the activated carbon adsorbent. Four different pore sizes (7 Å, 8.9 Å, 18.5 Å, and 27.9 Å) and three oxygen-containing functional groups (Carbonyl, Hydroxyl, and Carboxyl) were selected to model the graphite structures. Results from the GCMC simulation reveal a significant rise in the CO2 adsorption capacity (from 4 mmol/g to 21 mmol/g) as the pore size was increased from 7 Å to 27.9 Å. Likewise, the functional groups enhance the low-pressure adsorption process by reducing the onset pressure of the pore filling by a factor of 100, especially in ultra-micropores. Likewise, we demonstrate the increase in the isosteric heat of adsorption due to the reduction in the pore size and the presence of functional groups. Additionally, the study illustrates the adsorbed phase behaviour of CO2 concerning the pore characteristics, a facet often overlooked in the existing literature. The adsorbed phase local density and molecular orientation distribution are analysed to understand the variation in the adsorption uptake and isosteric heat of adsorption properties. The study further identifies the adsorbed phase monolayer to multilayer transition and the ‘T′-shaped orientation of the adsorbed CO2 molecules as the key contributors to the high isosteric heat of adsorption in 8.9 Å pore size. It is envisaged that this study will navigate the precision adsorbent development for an efficient carbon capture process.