How Collective Phenomena Impact CO2Reactivity and Speciation in Different Media

Daniela Polino, Daniela Polino, Emanuele Grifoni, Roger Rousseau, Michele Parrinello, Michele Parrinello, Michele Parrinello, Vassiliki Alexandra Glezakou

Research output: Contribution to journalArticlepeer-review

14 Scopus citations

Abstract

CO2 has attracted considerable attention in recent years due to its role in the greenhouse effect and environmental management. While its reaction with water has been studied extensively, the same cannot be said for reactivity in the supercritical CO2 phase, where the conjugate acid/base equilibria proceed through different mechanisms and activation barriers. In spite of the apparent simplicity of the CO2 + H2O reaction, the collective effect of different environments has a drastic influence on the free energy profile. Enhanced sampling techniques and well-tailored collective variables provide a detailed picture of the enthalpic and entropic drivers underscoring the differences in the formation mechanism of carbonic acid in the gas, aqueous, and supercritical CO2 phases.

Original languageEnglish
Pages (from-to)3963-3975
Number of pages13
JournalJournal of Physical Chemistry A
Volume124
Issue number20
DOIs
StatePublished - May 21 2020
Externally publishedYes

Funding

V.-A.G. and R.R. were supported by the U.S. Department of Energy (DOE), Office of Science, Office of Basic Energy Sciences, Division of Chemistry, Geochemistry and Biological Sciences, and located at Pacific Northwest National Laboratory (PNNL). Computational resources were provided by National Energy Research Scientific Computing Center (NERSC), a DOE Office of Science User Facility located at Lawrence Berkeley National Laboratory (LBNL). PNNL is operated by Battelle for the US Department of Energy under Contract DE-AC05-76RL01830. D.P., E.G. and M.P. thankfully acknowledge the financial support provided by the NCCR MARVEL, funded by the Swiss National Science Foundation, and the European Union Grant No. ERC-2014-AdG-670227/VARMET. Computational resources were provided by the Swiss National Supercomputing Centre (CSCS) under project IDs p503, s768, and s910.

FundersFunder number
Division of Chemistry, Geochemistry and Biological Sciences
Office of Basic Energy Sciences
US Department of EnergyDE-AC05-76RL01830
U.S. Department of Energy
Office of Science
Horizon 2020 Framework Programme670227
Pacific Northwest National Laboratory
European Commission
Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
National Center of Competence in Research Materials’ Revolution: Computational Design and Discovery of Novel Materials

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