Highly Surface-Active Ca(OH)2 Monolayer as a CO2 Capture Material

V. Ongun Özçelik, Kai Gong, Claire Emily White

Research output: Contribution to journalArticlepeer-review

24 Scopus citations


Greenhouse gas emissions originating from fossil fuel combustion contribute significantly to global warming, and therefore the design of novel materials that efficiently capture CO2 can play a crucial role in solving this challenge. Here, we show that reducing the dimensionality of bulk crystalline portlandite results in a stable monolayer material, named portlandene, that is highly effective at capturing CO2. On the basis of theoretical analysis comprised of ab initio quantum mechanical calculations and force-field molecular dynamics simulations, we show that this single-layer phase is robust and maintains its stability even at high temperatures. The chemical activity of portlandene is seen to further increase upon defect engineering of its surface using vacancy sites. Defect-containing portlandene is capable of separating CO and CO2 from a syngas (CO/CO2/H2) stream, yet is inert to water vapor. This selective behavior and the associated mechanisms have been elucidated by examining the electronic structure, local charge distribution, and bonding orbitals of portlandene. Additionally, unlike conventional CO2 capturing technologies, the regeneration process of portlandene does not require high temperature heat treatment because it can release the captured CO2 by application of a mild external electric field, making portlandene an ideal CO2 capturing material for both pre- and postcombustion processes.

Original languageEnglish (US)
Pages (from-to)1786-1793
Number of pages8
JournalNano Letters
Issue number3
StatePublished - Mar 14 2018

All Science Journal Classification (ASJC) codes

  • General Chemistry
  • Condensed Matter Physics
  • Mechanical Engineering
  • Bioengineering
  • General Materials Science


  • 2D materials
  • CO capture
  • Ca(OH)
  • portlandite


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