An interaction of 1,10-phenantroline with the copper electrode in neutral and acidic aqueous solutions: a surface enhanced Raman scattering study

Citation
K. Zawada et J. Bukowska, An interaction of 1,10-phenantroline with the copper electrode in neutral and acidic aqueous solutions: a surface enhanced Raman scattering study, J MOL STRUC, 555, 2000, pp. 425-432
Citations number
13
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
JOURNAL OF MOLECULAR STRUCTURE
ISSN journal
00222860 → ACNP
Volume
555
Year of publication
2000
Pages
425 - 432
Database
ISI
SICI code
0022-2860(20001128)555:<425:AIO1WT>2.0.ZU;2-R
Abstract
This paper presents the investigations of the Cu electrode/1,10-phenanthrol ine interface by using surface enhanced Raman scattering (SERS) method. Bot h neutral and acidic aqueous solutions of I,10-phenanthroline have been stu died. In order to characterise the adsorbed film its SERS spectrum was comp ared with the normal Raman spectra of 1,10-phenanthroline monohydrate and i ts complex with copper (I) chloride in a solid state. Both frequency values and relative intensities are considerably changed in the SERS spectra in c omparison to the Raman spectrum of non-adsorbed molecules. The general patt ern of the SERS spectrum is similar to that of the Raman spectrum of the Cu (I)-phenanthroline complex, thus suggesting that the Cu electrode surface is modified by some kind of surface complex. This surface complex was shown to be stable in a wide range of electrode potentials (up to -1.2 V. As evi denced by electrochemical experiments (cyclic voltammetry) the modification of the Cu surface by phenanthroline molecules significantly inhibits the h ydrogen evolution at negative potentials. The inhibiting effect is more pro nounced in acidic solutions. The appearance of the bands assigned to the ou t-of-plane vibrations in the surface Raman spectrum suggests that the plane of the adsorbed molecules is tilted from the normal to the metal surface. (C) 2000 Elsevier Science B.V. All rights reserved.