https://ogma.newcastle.edu.au/vital/access/ /manager/Index en-au 5 AFM and STM studies on the surface interaction of (BMP)TFSA and (EMIm)TFSA ionic liquids with Au(111) https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:7589 Wed 22 Mar 2023 16:41:40 AEDT ]]> An in situ STM/AFM and impedance spectroscopy study of the extremely pure 1-butyl-1-methylpyrrolidinium tris(pentafluoroethyl)trifluorophosphate/Au(111) interface: potential dependent solvation layers and the herringbone reconstruction https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:13606 Sat 24 Mar 2018 10:35:51 AEDT ]]> The interface ionic liquid(s)/electrode(s): In situ STM and AFM measurements https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:14181 Sat 24 Mar 2018 08:24:52 AEDT ]]> Effect of dissolved LiCl on the ionic liquid-Au(111) interface: an <i>in situ</i> STM study https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:21028 in situ scanning tunnelling microscopy (STM) has been employed to elucidate the structure of the charged Au(111)–ionic liquid (1-butyl-1-methylpyrrolidinium tris(pentafluoroethyl)trifluorophosphate, [Py1,4]FAP) interface in the presence of 0.1 M LiCl. The addition of the Li salt to the ionic liquid has a strong influence on the interfacial structure. In the first STM scan in situ measurements reveal that Au(111) undergoes the (22 x √3) 'herringbone' reconstruction in a certain potential regime, and there is strong evidence that the gold surface dissolves at negative electrode potentials in [Py1,4]FAP containing LiCl. Bulk deposition of Li is obtained at −2.9 V in the second STM scan.]]> Sat 24 Mar 2018 07:50:31 AEDT ]]>