Efficient CO2 capture by porous, nitrogen-doped carbonaceous adsorbents derived from task-specific ionic liquids

Research output: Contribution to journalArticlepeer-review

103 Scopus citations

Abstract

The search for a better carbon dioxide (CO2) capture material is attracting significant attention because of an increase in anthropogenic emissions. Porous materials are considered to be among the most promising candidates. A series of porous, nitrogen-doped carbons for CO2 capture have been developed by using high-yield carbonization reactions from task-specific ionic liquid (TSIL) precursors. Owing to strong interactions between the CO2 molecules and nitrogen-containing basic sites within the carbon framework, the porous nitrogen-doped compound derived from the carbonization of a TSIL at 500 °C, CN500, exhibits an exceptional CO 2 absorption capacity of 193 mg of CO2 per g sorbent (4.39 mmol g-1 at 0 °C and 1 bar), which demonstrates a significantly higher capacity than previously reported adsorbents. The application of TSILs as precursors for porous materials provides a new avenue for the development of improved materials for carbon capture. The art of capturing CO2: A series of porous, nitrogen-doped carbons for CO2 capture have been developed from task-specific ionic liquid (TSIL) precursors by using high-yield carbonization reactions. The porous, nitrogen-doped compound derived from the carbonization of a TSIL exhibits an exceptional CO2 absorption capacity (at 0 °C and 1 bar) because of strong interactions between the CO2 molecules and nitrogen-containing basic sites within the carbon framework.

Original languageEnglish
Pages (from-to)1912-1917
Number of pages6
JournalChemSusChem
Volume5
Issue number10
DOIs
StatePublished - Oct 2012

Keywords

  • adsorption
  • carbon
  • carbon dioxide fixation
  • ionic liquids
  • nitrogen

Fingerprint

Dive into the research topics of 'Efficient CO2 capture by porous, nitrogen-doped carbonaceous adsorbents derived from task-specific ionic liquids'. Together they form a unique fingerprint.

Cite this