Electrodeposition of manganese layers from sustainable sulfate based electrolytes
Functional manganese-(Mn)-containing layers are becoming increasingly important in the fields of sacrificial corrosion protection, biodegradable medical devices or electrochemical energy conversion systems. Electrodeposition can be a low cost and time-efficient production route, but the very electro...
| Autores: | , , , , , , |
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| Tipo de recurso: | artículo |
| Fecha de publicación: | 2018 |
| País: | España |
| Institución: | Universitat Autònoma de Barcelona |
| Repositorio: | Dipòsit Digital de Documents de la UAB |
| Idioma: | inglés |
| OAI Identifier: | oai:ddd.uab.cat:203890 |
| Acceso en línea: | https://ddd.uab.cat/record/203890 https://dx.doi.org/urn:doi:10.1016/j.surfcoat.2017.11.028 |
| Access Level: | acceso abierto |
| Palabra clave: | Mn electrodeposition PH control Sustainable electrolyte (NH4)2SO4 GD-OES XPS |
| Sumario: | Functional manganese-(Mn)-containing layers are becoming increasingly important in the fields of sacrificial corrosion protection, biodegradable medical devices or electrochemical energy conversion systems. Electrodeposition can be a low cost and time-efficient production route, but the very electronegative nature of Mn makes this reduction process quite challenging. In this paper, electrolytic potentiostatic deposition of metallic Mn layers from environmentally friendly aqueous manganese sulfate electrolytes with pH 3 is successfully demonstrated. A continuous electrolyte flow in the cathodic compartment of the electrochemical cell for controlling the pH value during deposition was found to be essential for achieving good layer qualities. Based on cyclic voltammetry analysis in combination with quartz crystal microbalance measurements a suitable deposition potential range was identified. The obtained electrodeposited layers were characterized by means of SEM, XRD, GD-OES and XPS. The shift of the deposition potential from - 2.4 VMSE to - 2.6 VMSE (deposition time 60 min) yields a thickness increase of the metallic α-Mn deposits from < 500 nm to ~ 2 μm. Only thin additional surface regions of Mn-oxides/-hydroxides were identified. The important role of (NH4)2SO4 as complex-forming electrolyte additive is discussed and an impact of the salt concentration on the deposit properties is revealed. This is a promising starting point for further Mn alloy deposition analysis. |
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