Nalazite se na CroRIS probnoj okolini. Ovdje evidentirani podaci neće biti pohranjeni u Informacijskom sustavu znanosti RH. Ako je ovo greška, CroRIS produkcijskoj okolini moguće je pristupi putem poveznice www.croris.hr
izvor podataka: crosbi

Determination of Surface Potential from the Electrode Potential of a Single-Crystal Electrode (CROSBI ID 134440)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Kallay, Nikola ; Preočanin, Tajana ; Ivšić, Trpimir Determination of Surface Potential from the Electrode Potential of a Single-Crystal Electrode // Journal of colloid and interface science, 309 (2007), 1; 21-27. doi: 10.1016/j.jcis.2006.10.075

Podaci o odgovornosti

Kallay, Nikola ; Preočanin, Tajana ; Ivšić, Trpimir

engleski

Determination of Surface Potential from the Electrode Potential of a Single-Crystal Electrode

Determination of surface potentials Ψ 0 at the metal oxide/aqueous solution interface from measured electrode potentials of a metal oxide single crystal electrode (SCrE) is described. The proposed method is based on the Surface Complexation Model and evaluates the surface potential at the isoelectric point i.e. at pHiep. This value is used for calculation of Ψ 0 values from the measured electrode potentials. Both 1-pK and 2-pK models produced the same result so that the procedure does not depend on the assumed mechanism of the surface charging. It is proposed to determine the pristine point of zero charge pHeln and the isoelectric point pHiep, and use these data to set the scale of surface potentials. The value of pHeln can be obtained at a sufficiently low ionic strength where pHpzc coincides with pHiep. The method is demonstrated on the example of the anatase single crystal electrode. From the shifts of pHiep and pHpzc with respect to the pristine point of zero charge pHeln it was concluded that Cl– ions exhibit higher affinity for association with positively charged surface groups than ClO4– ions. Also, preferential surface association of Na+ cations compared to both anions was detected. The slopes of the Ψ 0(pH) functions were found to be significantly lower in magnitude with respect to the Nernst equation which is due to high degree of counterion association at the surface caused by their relatively high concentration.

surface potential; surface charge; single crystal electrode; surface complexation model; electrical interfacial layer; anatase

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

Podaci o izdanju

309 (1)

2007.

21-27

objavljeno

0021-9797

10.1016/j.jcis.2006.10.075

Povezanost rada

Kemija

Poveznice
Indeksiranost