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Title: Surface enhanced Raman spectroscopy of iron oxide thin films: Comparison with the passive film on iron

Journal Article · · Journal of the Electrochemical Society
DOI:https://doi.org/10.1149/1.1837648· OSTI ID:511942
; ;  [1];  [2]
  1. Univ. of California, Berkeley, CA (United States). Dept. of Materials Science and Mineral Engineering
  2. Swiss Federal Inst. of Tech., Zurich (Switzerland). Inst. of Materials Chemistry and Corrosion

Thin films (33 nm to 1.4 {micro}m) of iron oxides were deposited onto roughened silver substrates by laser ablation of Fe{sub 3}O{sub 4} and {gamma}-Fe{sub 2}O{sub 3} targets. Surface enhanced Raman (SER) spectra from the 33 to 37 nm thick films, both in air and in aqueous borate buffer (pH 8.4), were identical to SER spectra of the passive film formed on iron in the same solution; that is, all were characterized by a strong broad peak centered at approximately 530 to 580 cm{sup {minus}1}. The 33 to 37 nm thick films were potentiodynamically reduced in borate buffer. Electrochemical reduction of the ablated iron oxide films initiated at a more cathodic potential than that found for the passive film on iron. Thicker 178 nm films formed by laser ablation of Fe{sub 3}O{sub 4} exhibited spectra partially resembling the iron passive film and partially resembling the normal Raman spectrum of bulk Fe{sub 3}O{sub 4}. The 153 nm and 1.4 {micro}m thick films formed from Fe{sub 2}O{sub 3} and 1.3 {micro}m thick films formed from Fe{sub 3}O{sub 4} gave very weak Raman spectra that were characteristic of the bulk oxides, and did not resemble the iron passive film. The observation that the SER spectra from passive films on iron, as measured in this and previous studies, are identical to the SER spectra from thin films laser ablated from targets of Fe{sub 3}O{sub 4} and Fe{sub 2}O{sub 3} (in both cases, resulting in iron oxides most probably hydrated and of small particle size) permits the more accurate assignment of spectral features in future, as well as past SERS studies.

Sponsoring Organization:
Electric Power Research Inst., Palo Alto, CA (United States)
OSTI ID:
511942
Journal Information:
Journal of the Electrochemical Society, Vol. 144, Issue 5; Other Information: PBD: May 1997
Country of Publication:
United States
Language:
English

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