Near-Ambient Pressure XPS and NEXAFS Study of a Superbasic Ionic Liquid with CO2

被引:9
|
作者
Cole, Jordan [1 ]
Henderson, Zoe [1 ]
Thomas, Andrew G. [2 ,3 ]
Compean-Gonzalez, Claudia L. [2 ,3 ]
Greer, Adam J. [4 ]
Hardacre, Christopher [4 ]
Venturini, Federica [5 ]
Garzon, Wilson Quevedo [5 ]
Ferrer, Pilar [5 ]
Grinter, David C. [5 ]
Held, Georg [5 ]
Syres, Karen L. [1 ]
机构
[1] Univ Cent Lancashire, Jeremiah Horrocks Inst Math, Phys & Astron, Preston PR1 2HE, Lancs, England
[2] Univ Manchester, Photon Sci Inst, Dept Mat Sci, Manchester M13 9PL, Lancs, England
[3] Univ Manchester, Henry Royce Inst, Manchester M13 9PL, Lancs, England
[4] Univ Manchester, Dept Chem Engn & Analyt Sci, Manchester M13 9PL, Lancs, England
[5] Diamond Light Source, Didcot OX11 0DE, Oxon, England
关键词
CARBON CAPTURE; ADSORPTION; SURFACE; TETRAFLUOROBORATE; BENZOTRIAZOLE; INTERFACE; ULTRATHIN; ENERGY; FILMS;
D O I
10.1021/acs.jpcc.1c05738
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In situ photoemission and near-edge X-ray absorption fine structure (NEXAFS) techniques have been used to study the interaction of CO2 with an ionic liquid thin film. A thin film of the superbasic ionic liquid (SBIL) trihexyltetradecylphosphonium benzimidazolide ([P-66614][benzim]) was prepared on a rutile TiO2 (110) surface and exposed to CO2 at near-ambient pressures. NEXAFS measurements combined with density functional theory calculations indicate a realignment of [benzim](-) anions from 27 degrees from the surface normal to 54 degrees upon exposure to CO2. Angle-resolved X-ray photoelectron spectroscopy (AR-XPS) shows evidence of irreversible CO2 absorption in thin films of [P-66614][benzim] and a greater concentration of CO2-reacted anions in the deeper layers. These results give a new perspective on CO2 uptake in ionic liquids and fundamental interactions at the liquid-gas interface. Understanding this interfacial behavior is important for developing ILs for gas capture applications and may influence the performance of other IL-based technologies.
引用
收藏
页码:22778 / 22785
页数:8
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