Photocurrents flowing at AISI 301 stainless steel electrodes, polarized anodically in sulfate solutions of various pH, were related to the nature of the surface oxides formed in these environments. The oxides were identified by surface Raman and IR spectroscopies. Correlations among pH, surface coverage with different types of oxides and photocurrent were recognized by mapping Raman spectroscopy, optical microscopy and image analysis. A high photoresponse is mainly related to high surface coverage with magnetite, formed at high pH. Exposure to low-pH solutions gives rise to preferential formation of hematite. Magnetite formed at high pH is irreversibly transformed into hematite if the oxide layer is subsequently exposed to a low-pH solution.

A photoelectrochemical and spectroscopic investigation of oxide layers on AISI 301 in sulfate solutions at different pH

Maffi S;
2004

Abstract

Photocurrents flowing at AISI 301 stainless steel electrodes, polarized anodically in sulfate solutions of various pH, were related to the nature of the surface oxides formed in these environments. The oxides were identified by surface Raman and IR spectroscopies. Correlations among pH, surface coverage with different types of oxides and photocurrent were recognized by mapping Raman spectroscopy, optical microscopy and image analysis. A high photoresponse is mainly related to high surface coverage with magnetite, formed at high pH. Exposure to low-pH solutions gives rise to preferential formation of hematite. Magnetite formed at high pH is irreversibly transformed into hematite if the oxide layer is subsequently exposed to a low-pH solution.
2004
AISI 301
IR spectroscopy
photoelectrochemistry
Raman spectroscopy
stainless steel
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/11468
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus ND
  • ???jsp.display-item.citation.isi??? ND
social impact