Study on the performance of an improved Ti/SnO sub(2)-Sb sub(2)O sub(3)/PbO sub(2) based on porous titanium substrate compared with planar titanium substrate
This present work focused on systematically studying the effect of a porous Ti substrate on the surface structure and electrochemical properties of lead dioxide electrodes prepared by anodic deposition under galvanostatic conditions. Characterization experiments, including scanning electron microsco...
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Veröffentlicht in: | RSC advances 2015-03, Vol.5 (34), p.26530-26539 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | This present work focused on systematically studying the effect of a porous Ti substrate on the surface structure and electrochemical properties of lead dioxide electrodes prepared by anodic deposition under galvanostatic conditions. Characterization experiments, including scanning electron microscopy (SEM), X-ray diffraction (XRD), linear sweep voltammetry (LSV), cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), accelerated life time testing and a degradation experiment of methylene blue trihydrate were performed to determine the effect of different Ti substrates. Compared with the planar Ti substrate, the results showed that the porous Ti substrate decreased the grain size of lead dioxide and formed a compact and fine surface coating. The electrode had smaller crystalline particles and a more compact structure. The porous Ti/SnO sub(2)-Sb sub(2)O sub(3)/PbO sub(2) electrode had a higher oxygen evolution overpotential, a larger active surface area and higher electrochemical activity. The lifetime of the porous Ti/SnO sub(2)-Sb sub(2)O sub(3)/PbO sub(2) electrode (214 h) was 3.69 times higher than that of the planar Ti/SnO sub(2)-Sb sub(2)O sub(3)/PbO sub(2) electrode (58 h). Moreover, the degradation rate constant of methylene blue trihydrate on the porous Ti substrate lead dioxide electrode (0.03868 min super(-1)) was 1.52 times than that of the planar Ti substrate lead dioxide electrode (0.02542 min super(-1)). |
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ISSN: | 2046-2069 |
DOI: | 10.1039/c4ra13492c |