| Autor: |
Roman Eschenbacher, Tanja Bauer, Hanna Bühlmeyer, Tao Xu, Peter Wasserscheid, Nicola Taccardi, Jörg Libuda, Christian Schuschke |
| Rok vydání: |
2021 |
| Předmět: |
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| Zdroj: |
The journal of physical chemistry letters. 12(41) |
| ISSN: |
1948-7185 |
| Popis: |
We used temperature-programmed infrared reflection absorption spectroscopy (TP-IRAS) to study the desorption behavior of CO on Pt(111) coadsorbed with four kinds of ionic liquids (ILs), namely 1-butyl-1-methyl-pyrrolidinium-bis(trifluoromethylsulfonyl)imide ([C4C1Pyr][NTf2]), 1-ethyl-3-methyl-imidazolium-bis(trifluoromethylsulfonyl)imide ([C2C1Im][NTf2]), 1-butyl-1-methyl-pyrrolidinium-trifluoro-methanesulfonate ([C4C1Pyr][OTf]), and 1-butyl-1-methyl-pyrrolidinium-hexafluorophosphate ([C4C1Pyr][PF6]). We found that CO desorbs earlier from a Pt(111) surface with coadsorbed ILs than without. In addition, the CO desorption temperature varies between different types of coadsorbed ILs, which follows the order: [C4C1Pyr][PF6] (365 K) > [C4C1Pyr][NTf2] (362 K) > [C2C1Im][NTf2] (352 K) > [C4C1Pyr][OTf] (348 K). We ascribe the difference in CO desorption temperature to the different interaction strength between ILs and the Pt(111) surface. A stronger IL-Pt(111) interaction leads to a lower CO desorption temperature. We suggest that TP-IRAS experiments of CO coadsorbed with ILs can be a useful method to aid the characterization of the interaction strength between ILs and metal surfaces such as Pt(111). |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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