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Fabrication, characterization and electrocatalytic application of a lead dioxide electrode with porous titanium substrate
In this study, PbO2 electrode was prepared on porous Ti/SnO2–Sb2O5 substrate (denoted as 3D-Ti/PbO2 electrode), and its electrochemical properties were investigated in detail. The electrodeposition mechanism of 3D-Ti/PbO2 electrode was investigated by cyclic voltammetry (CV) and electrochemical impe...
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Published in: | Journal of alloys and compounds 2015-11, Vol.650, p.705-711 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | In this study, PbO2 electrode was prepared on porous Ti/SnO2–Sb2O5 substrate (denoted as 3D-Ti/PbO2 electrode), and its electrochemical properties were investigated in detail. The electrodeposition mechanism of 3D-Ti/PbO2 electrode was investigated by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). Scanning electron microscope (SEM) result showed that the 3D-Ti/PbO2 electrode possessed porous structure when it was electrodeposited for time less than 30 min. The 3D-Ti/PbO2 electrode prepared for 10 min had more active sites than the lead dioxide electrode electrodeposited on planar titanium substrate (denoted as 2D-Ti/PbO2 electrode) and its electrochemical porosity is about 54%. The embedded structure between porous Ti/SnO2–Sb2O5 substrate and PbO2 coating increased the stability of 3D-Ti/PbO2 electrode. The service life of 3D-Ti/PbO2 electrode was about 350 h which was much longer than 2D-Ti/PbO2 electrode. What's more, 3D-Ti/PbO2 electrode had better electrocatalytic activity towards phenol degradation than 2D-Ti/PbO2 electrode.
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•3D-Ti/PbO2 electrode was prepared on a porous titanium substrate.•The electrochemical active surface area was investigated.•The activity of 3D-Ti/PbO2 electrode towards phenol oxidation was investigated.•3D-Ti/PbO2 electrode shows superior electrocatalytic activity. |
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ISSN: | 0925-8388 1873-4669 |
DOI: | 10.1016/j.jallcom.2015.07.222 |