The adsorption of iso-valeronitrile (IVN) on Ag single crystal face electrodes was studied by means of capacitance measurements at near zero frequency in aqueous 0.15 M NaClO4 as a supporting electrolyte solution. Experimental data have shown that adsorption increases in the sequence of crystal faces (1 1 0)less than (1 0 0) LT (1 1 1) LT Hg. Differently from acetonitrile adsorption, the mode of adsorption of IVN is attributable to hydrophilic hydrophobic interactions resulting in a squeezing-out mechanism. The crystal face sequence is governed by Agwater interactions which are thus confirmed to vary in the order (1 1 0) (1 0 0) (1 1 1). Although never observed with Hg, below a critical value of the squeezing-out effect, neutral organic compounds are unable to displace the first layer of water molecules adsorbed on a solid metal surface
Effect of the molecular structure on the adsorption of nitriles on Ag single crystal face electrodes: iso-valeronitrile vs. acetonitrile
2003
Abstract
The adsorption of iso-valeronitrile (IVN) on Ag single crystal face electrodes was studied by means of capacitance measurements at near zero frequency in aqueous 0.15 M NaClO4 as a supporting electrolyte solution. Experimental data have shown that adsorption increases in the sequence of crystal faces (1 1 0)less than (1 0 0) LT (1 1 1) LT Hg. Differently from acetonitrile adsorption, the mode of adsorption of IVN is attributable to hydrophilic hydrophobic interactions resulting in a squeezing-out mechanism. The crystal face sequence is governed by Agwater interactions which are thus confirmed to vary in the order (1 1 0) (1 0 0) (1 1 1). Although never observed with Hg, below a critical value of the squeezing-out effect, neutral organic compounds are unable to displace the first layer of water molecules adsorbed on a solid metal surfaceI documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
