Microstructural probing of phosphonium-based ionic liquids on a gold electrode using colloid probe AFMShow others and affiliations
2022 (English)In: Physical Chemistry, Chemical Physics - PCCP, ISSN 1463-9076, E-ISSN 1463-9084, Vol. 24, no 41, p. 25411-25419Article in journal (Refereed) Published
Abstract [en]
Atomic force microscopy (AFM) with a gold colloid probe modeled as the electrode surface is employed to directly capture the contact resonance frequency of two phosphonium-based ionic liquids (ILs) containing a common anion [BScB]− and differently lengthened cations ([P6,6,6,14]+ and [P4,4,4,8]+). The comparative interfacial studies are performed by creating IL films on the surface of gold, followed by measuring the wettability, thickness of the films, adhesion forces, surface morphology and AFM-probed contact resonance frequency. In addition, the cyclic voltammetry and impedance spectroscopy measurements of the neat ILs are measured on the surface of the gold electrode. The IL with longer cation alkyl chains exhibits a well-defined thin film on the electrode surface and enhanced the capacitance than the shorter chain IL. The AFM contact resonance frequency and force curves reveal that the longer IL prefers to form stiffer ion layers at the gold electrode surface, suggesting the “…anion–anion–cation–cation…” bilayer structure, in contrast, the shorter-chain IL forms the softer cation–anion alternating structure, i.e., “…anion–cation–anion–cation…”.
Place, publisher, year, edition, pages
Royal Society of Chemistry, 2022. Vol. 24, no 41, p. 25411-25419
National Category
Physical Chemistry
Research subject
Chemistry of Interfaces
Identifiers
URN: urn:nbn:se:ltu:diva-93461DOI: 10.1039/d2cp02489fISI: 000868733600001PubMedID: 36250344Scopus ID: 2-s2.0-85140933201OAI: oai:DiVA.org:ltu-93461DiVA, id: diva2:1701181
Funder
Swedish Research Council, 2018-04133
Note
Validerad;2022;Nivå 2;2022-11-17 (hanlid);
Funder: China Postdoctoral Science Foundation, Natural Science Foundation of Jiangsu Province (BK20191289); National Natural Science Foundation of China (21978134, 21838004, and 22108015)
2022-10-052022-10-052022-11-17Bibliographically approved