Loading…
Growth and properties of Cr-rich thick and porous oxide films on Type 304 stainless steel formed by square wave potential pulse polarisation
Extraordinarily thick and porous oxide films are obtained on Type 304 stainless steel. The material was polarised in 5 kmol m −3 H 2SO 4 solution at 50–80 °C with applied potential modulated as square wave. The films formed are classified into two types according to applied potentials. For the anodi...
Saved in:
Published in: | Electrochimica acta 2001-11, Vol.47 (4), p.543-551 |
---|---|
Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Extraordinarily thick and porous oxide films are obtained on Type 304 stainless steel. The material was polarised in 5 kmol
m
−3 H
2SO
4 solution at 50–80
°C with applied potential modulated as square wave. The films formed are classified into two types according to applied potentials. For the anodic type, Fe and Cr actively dissolve at the lower potential of the square wave,
E
L, into Fe
2+ and Cr
2+, then re-oxidise at the higher potential,
E
H, to be mainly Cr
3+ oxide. Alternatively, for the cathodic type, Fe and Cr dissolve at
E
H, which is in the transpassive region, then the dissolved Cr
6+ ions are reduced into Cr
3+ oxide at
E
L. Transmission electron microscopy showed that the porous film consists of nanocrystalline grains of around 20–30 nm in diameter, and has many pathways linking each other to be penetrated by ions and water molecular easily. The porous layer is basically composed of Cr
2FeO
4 spinel oxide with excess Cr. The chemical composition, particle size, and also lattice parameter could be controlled by changing
E
H,
E
L, and the width of the potential pulse,
t
H and
t
L. The porous oxide films formed by square wave potential pulse polarisation might be applied for various surface functional materials, i.e. a carrier of catalyst, oxide electrode, and biocompatible materials. |
---|---|
ISSN: | 0013-4686 1873-3859 |
DOI: | 10.1016/S0013-4686(01)00782-4 |