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Temporal Response of SERS to the Potential for 4‐Cyanopyridine Adsorbed on Ag Electrode
Author(s) -
Chang Hua,
Lee Long Jeng,
Sheu Ung Hua
Publication year - 1993
Publication title -
journal of the chinese chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.329
H-Index - 45
eISSN - 2192-6549
pISSN - 0009-4536
DOI - 10.1002/jccs.199300065
Subject(s) - chemistry , electrode , adsorption , raman scattering , electrode potential , raman spectroscopy , desorption , analytical chemistry (journal) , electrochemistry , standard electrode potential , nanotechnology , optics , organic chemistry , materials science , physics
Time‐resolved surface‐enhanced Raman scattering (SERS) was applied to study the response of Raman bands from 4‐cyanopyridine (PyCN) adsorbed on a Ag electrode to variation of the potential; the temporal resolution was 0.1 s. The response of the SERS signals of PyCN was instantaneous to the oxidation potential of Ag electrode. However, delay of the SERS signals was observed while AgCl was reducing. The decay and growth of the SERS bands look place within 1 s in the cases of desorption and adsorption of PyCN on the electrode. It took much longer for PyCN to alter from one adsorption geometry to another on the electrode.