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Sökning: id:"swepub:oai:lup.lub.lu.se:07940e2f-09c0-453d-9bac-c43288695b42" > In situ XPS of comp...

In situ XPS of competitive CO2/H2O absorption in an ionic liquid

Cole, Jordan (författare)
University of Central Lancashire
Henderson, Zoë (författare)
University of Central Lancashire
Thomas, Andrew G. (författare)
University of Manchester
visa fler...
Castle, Christopher (författare)
University of Manchester
Greer, Adam J. (författare)
University of Manchester
Hardacre, Christopher (författare)
University of Manchester
Scardamaglia, Mattia (författare)
Lund University,Lunds universitet,MAX IV-laboratoriet,MAX IV Laboratory
Shavorskiy, Andrey (författare)
Lund University,Lunds universitet,MAX IV-laboratoriet,MAX IV Laboratory
Syres, Karen L. (författare)
University of Central Lancashire
visa färre...
 (creator_code:org_t)
2023
2023
Engelska.
Ingår i: JPhys Materials. - 2515-7639. ; 6:4
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Superbasic ionic liquids (SBILs) are being investigated as potential carbon dioxide (CO2) gas capture agents, however, the presence of H2O in the flue stream can inhibit the uptake of CO2. In this study a thin film of the SBIL trihexyltetradecylphosphonium 1,2,4-triazolide ([P66614][124Triz]) was deposited onto rutile TiO2 (110) using in situ electrospray deposition and studied upon exposure to CO2 and H2O using in situ near-ambient pressure x-ray photoelectron spectroscopy (NAP-XPS). The molar uptake ratio of gas in the electrosprayed SBIL (n gas :n IL) was calculated to be 0.3:1 for CO2, 0.7:1 for H2O, and 0.9:1 for a CO2/H2O mixture. NAP-XPS taken at two different depths reveals that the competitive absorption of CO2 and H2O in [P66614][124Triz] varies with sampling depth. A greater concentration of CO2 absorbs in the bulk layers, while more H2O adsorbs/absorbs at the surface. The presence of H2O in the gas mixture does not inhibit the absorption of CO2. Measurements taken during exposure and after the removal of gas indicate that CO2 absorbed in the bulk does so reversibly, whilst CO2 adsorbed/absorbed at the surface does so irreversibly. This is contrary to the fully reversible CO2 reaction shown for bulk ionic liquids (ILs) in literature and suggests that irreversible absorption of CO2 in our highly-structured thin films is largely attributed to reactions at the surface. This has potential implications on IL gas capture and thin film IL catalysis applications.

Ämnesord

NATURVETENSKAP  -- Fysik -- Den kondenserade materiens fysik (hsv//swe)
NATURAL SCIENCES  -- Physical Sciences -- Condensed Matter Physics (hsv//eng)

Nyckelord

carbon capture
electrospray
ionic liquids
thin films
x-ray photoelectron spectroscopy

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