Cooperative Carbon Capture by a Novel Material that Mimics a Plant Enzyme

Innovative materials adsorb carbon dioxide via an unprecedented cooperative insertion mechanism.

default-alt-text — Image courtesy of Thomas McDonald, Jarad Mason, and Jeffrey Long

The Science

Researchers discovered a novel metal-organic framework (MOF) material that exhibits an unprecedented cooperative mechanism for carbon dioxide (CO₂) capture-and-release with only small shifts in temperature. This structure of the MOF, with CO₂ adsorbed, closely resembles the RuBisCO enzyme found in plants, which captures CO₂ from the atmosphere for conversion into nutrients.

The Impact

The discovery paves the way for designing more efficient materials that dramatically reduce overall energy cost of carbon capture. Such materials could be used for carbon capture from fossil-fuel-based power plants as well as from the atmosphere, mitigating the greenhouse effect.

Summary

A team of researchers at the Center for Gas Separations Relevant to Clean Energy Technologies, a DOE Energy Frontier Research Center led by the University of California, Berkeley, has discovered a cooperative mechanism for carbon dioxide (CO₂) adsorption in porous MOF materials. First, a CO₂ molecule gets inserted between a metal ion and an amine group within the cylindrical pore of the MOF. Interestingly, the chemical environment of the MOF with the adsorbed CO₂ is very similar to that of plant enzyme RuBisCO with a bound CO₂. RuBisCO plays an essential role in biological carbon fixation by plants and conversion into nutrients. In the case of the newly synthesized diamine-appended MOFs, however, the inserted CO₂ reorganizes the chemical environment at the adjacent metal ion site to be just right for the insertion of the next CO₂. As more CO₂ enters the pore, a cooperative domino effect ensues that leads to the formation of linear chains of ammonium carbamate along the cylindrical pore surfaces of the MOF. Gas adsorption measurements show the high selectivity of the material for CO₂ from the typical composition of flue gas from fossil-fuel-based power plants that contains nitrogen, water, and CO₂. Furthermore, the material has large working capacities – the amount of CO₂ adsorbed and desorbed for a given amount of material – that are enabled by only moderate temperature shifts for the adsorption and desorption processes. Finally, the research points out that changing the strength of the metal-diamine bond through metal substitution allows for rational tuning of the adsorption and desorption properties. The enhanced carbon capture efficiency of the new class of materials could allow for dramatic reductions in the overall energy cost of carbon capture in power plants or even from the atmosphere.

Contact

Jeffrey Long
University of California, Berkeley
[email protected]

Funding

Center for Gas Separations Relevant to Clean Energy Technologies, an Energy Frontier Research Center funded by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences under award DE-SC0001015 (materials characterization); Nanoporous Materials Genome Center of the U.S. Department of Energy, Office of Basic Energy Sciences, Division of Chemical Sciences, Geosciences, and Biosciences, under Award DE-FG02-12ER16362 (computation); Advanced Research Projects Agency-Energy (ARPA-E), U.S. Department of Energy, under Award Numbers DE-AR0000103 and DE-AR0000402 (materials synthesis and gas adsorption); Work by co-authors from Italy and Norway additionally supported by Italian grant MIUR-PRIN 2010-2011 and Research Council of Norway; National Science Foundation fellowship support for J.A. Mason.

Publications

T.M. McDonald, J.A. Mason, X. Kong, E.D. Bloch, D. Gygi, A. Dani, V. Crocellà, F. Giordanino, S.O. Odoh, W. Drisdell, B. Vlaisavljevich, A.L. Dzubak, R. Poloni, S.K. Schnell, N. Planas, K. Lee, T. Pascal, L.F. Wan, D. Prendergast, J.B. Neaton, B. Smit, J.B. Kortright, L. Gagliardi, S. Bordiga, J.A. Reimer, and J.R. Long, "Cooperative insertion of CO₂ in diamine-appended metal-organic frameworks.” Nature 2015, 519, 303-308. [DOI: 10.1038/nature14327]