Significantly Increased CO2 Adsorption Performance of Nanostructured Templated Carbon by Tuning Surface Area and Nitrogen Doping
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Abstract
Carbon dioxide adsorption properties of a series of templated carbon adsorbents with high Brunauer–Emmett–Teller surface areas (1361–3840 m2/g) and with/without nitrogen doping (6–7 wt % N) were systematically studied. Two linear relationships between CO2 adsorption capacities and surface areas of nitrogen-doped/undoped nanostructured templated carbons were first established. The doped nitrogen was present in the forms of pyridinic nitrogen, pyrrolic/pyridonic nitrogen, quaternary nitrogen, and an oxidized form of nitrogen. The interaction energies with CO2, as approximated by the isosteric heats of adsorption, were increased from 30 kJ/mol on the undoped carbon to 50 kJ/mol on the N-doped carbon as a result of these nitrogen sites. The increased interactions led to an enhancement in CO2 adsorption capacity by a factor of 2, while N2 uptake was not enhanced. The optimized N-doped templated carbon, N-TC-EMC, possessed remarkable CO2 capacity (4 mmol/g at 1 atm and 298 K) and selectivity (CO2/N2 at 1 atm = 14). Postdoping ammonia treatment was found beneficial to CO2 adsorption. CO2 performance of N-doped carbon under wet condition and conditions relevant to flue gas, rates of adsorption, and regeneration requirement, which are important for practical applications, were also investigated. The results showed that N-doped templated carbon exhibited all prerequisite attributes for CO2 capture and storage applications: high CO2 capacity and CO2/N2 selectivity, fast and reversible adsorption, thermal and moisture stabilities, and ease in CO2 desorption.
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