Pregled bibliografske jedinice broj: 310835
Determination of Surface Potential from the Electrode Potential of a Single-Crystal Electrode
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 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 310835 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Determination of Surface Potential from the Electrode Potential of a Single-Crystal Electrode
Autori
Kallay, Nikola ; Preočanin, Tajana ; Ivšić, Trpimir
Izvornik
Journal of Colloid and Interface Science (0021-9797) 309
(2007), 1;
21-27
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
surface potential; surface charge; single crystal electrode; surface complexation model; electrical interfacial layer; anatase
Sažetak
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.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
119-1191342-2961 - Fizikalna kemija koloida i međupovršina (Kallay, Nikola, MZOS ) ( CroRIS)
Ustanove:
Prirodoslovno-matematički fakultet, Zagreb
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
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- AGRICOLA
- BIOSIS Previews (Biological Abstracts)
- CA Search (Chemical Abstracts)
- EMBASE (Excerpta Medica)
- Chemical Engineering Abstracts
- Literature Abstracts/Catalysts and Catalysis
- Research Alert
- Science Abstracts
- Scopus