Tetrameric self-assembling of water-lean solvents enables carbamate anhydride-based CO2 capture chemistry

  • Julien Leclaire
  • , David J. Heldebrant
  • , Katarzyna Grubel
  • , Jean Septavaux
  • , Marc Hennebelle
  • , Eric Walter
  • , Ying Chen
  • , Jose Leobardo Bañuelos
  • , Difan Zhang
  • , Manh Thuong Nguyen
  • , Debmalya Ray
  • , Sarah I. Allec
  • , Deepika Malhotra
  • , Wontae Joo
  • , Jaelynne King

Research output: Contribution to journalArticlepeer-review

18 Scopus citations

Abstract

Carbon capture, utilization and storage is a key yet cost-intensive technology for the fight against climate change. Single-component water-lean solvents have emerged as promising materials for post-combustion CO2 capture, but little is known regarding their mechanism of action. Here we present a combined experimental and modelling study of single-component water-lean solvents, and we find that CO2 capture is accompanied by the self-assembly of reverse-micelle-like tetrameric clusters in solution. This spontaneous aggregation leads to stepwise cooperative capture phenomena with highly contrasting mechanistic and thermodynamic features. The emergence of well-defined supramolecular architectures displaying a hydrogen-bonded internal core, reminiscent of enzymatic active sites, enables the formation of CO2-containing molecular species such as carbamic acid, carbamic anhydride and alkoxy carbamic anhydrides. This system extends the scope of adducts and mechanisms observed during carbon capture. It opens the way to materials with a higher CO2 storage capacity and provides a means for carbamates to potentially act as initiators for future oligomerization or polymerization of CO2. (Figure presented.)

Original languageEnglish
Pages (from-to)1160-1168
Number of pages9
JournalNature Chemistry
Volume16
Issue number7
DOIs
StatePublished - Jul 2024

Funding

French authors were supported by the LABEX iMUST of the University of Lyon (ANR-10-LABX-0064), created within the ‘Plan France 2030’ set up by the French government and managed by the French National Research Agency (ANR) and by the Region Auvergne-Rhone Alpes (Pack Ambition Recherche 2019). US authors acknowledge the US Department of Energy, Office of Science, Basic Energy Sciences, Chemical Sciences, Geosciences, and Biosciences Division, Understanding and Control of Reactive Separations (FWP 75428). Data in this publication were obtained using the Pacific Northwest National Laboratory (PNNL) Catalysis Science NMR Facility. This research used resources of the National Energy Research Scientific Computing Center (NERSC), a US Department of Energy Office of Science User Facility located at Lawrence Berkeley National Laboratory, operated under contract no. DE-AC02-05CH11231. PNNL is operated by Battelle for the US Department of Energy under contract no. DE-AC05-76RL01830. We thank the Centre Commun de RMN of the Université Claude Bernard Lyon 1 (CCRMN UCBL) for assistance with NMR analyses, B. Mundy for help with technical editing and P. Koech for fruitful discussions.

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