In-situ investigations of the corrosion on metal surfaces
In-situ investigations of the corrosion on metal surfaces
Disciplines
Chemistry (50%); Physics, Astronomy (30%); Materials Engineering (20%)
Keywords
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In-Situ,
Corrosion,
Metals,
Atmosphere,
IRRAS,
TM-AFM
The oxidation behavior of pure metals and alloys has been a wide field of investigations during the last decades. While these previous studies mainly deal with multi-analytical ex-situ investigations of the corrosion products formed on a metal surface during degradation, the aim of this project is to elucidate the corrosion mechanism of pure metals and alloys in the early stages of corrosion in-situ by the aim of Tapping-Mode Atomic Force Microscopy (TM-AFM), InfraRed Reflection Absorption Spectroscopy (IRRAS) and Quartz Crystal Microbalance (QCM) as well as by additional ex-situ Secondary Ion Mass Spectrometry (SIMS) measurements. The main focus of this project is directed to the atmospheric corrosion behavior of pure silver and its alloys because of the vital role of these materials in modern semiconductor devices due to the lowest electrical resistivity in metals. Already a thin tarnish film on silver can influence the operational readiness negatively particularly with regard to the nowadays occurring miniaturization of such units. Therefore the knowledge of the exact reaction mechanism of the weathering process is necessary to develop strategies and methods to prevent these reactions. Furthermore the application of silver nano-particles as integral part for the microbial inhibition of synthetic potable water containers requires investigations of the corrosion mechanism. Even though there were diversified ex-situ investigations of the tarnishing process of pure silver there is still a lack of the detailed knowledge of the reaction mechanism taking place during weathering with or without acidifying gases such as SO2, OCS or NOx. As could be shown in previous studies on copper and its alloys there is a discrepancy of the results obtained by in-situ methods to those used for the identification of the corrosion products ex-situ. The project aim is to clarify the exact mechanism of the silver oxidation and sulfidation by atmospheric pollutants such as SO2, NO2, and H2S in dependence of the humidity content of the surrounding atmosphere as well as the influence of alloy constituents such as gold. The influence of other oxidation parameters such as UV-light shall also be clarified within this project.
The oxidation behavior of pure metals and alloys has been a wide field of investigations during the last decades. While these previous studies mainly deal with multi-analytical ex-situ investigations of the corrosion products formed on a metal surface during degradation, the aim of this project is to elucidate the corrosion mechanism of pure metals and alloys in the early stages of corrosion in-situ by the aim of Tapping-Mode Atomic Force Microscopy (TM-AFM), InfraRed Reflection Absorption Spectroscopy (IRRAS) and Quartz Crystal Microbalance (QCM) as well as by additional ex-situ Secondary Ion Mass Spectrometry (SIMS) measurements. The main focus of this project is directed to the atmospheric corrosion behavior of pure silver and its alloys because of the vital role of these materials in modern semiconductor devices due to the lowest electrical resistivity in metals. Already a thin tarnish film on silver can influence the operational readiness negatively particularly with regard to the nowadays occurring miniaturization of such units. Therefore the knowledge of the exact reaction mechanism of the weathering process is necessary to develop strategies and methods to prevent these reactions. Furthermore the application of silver nano-particles as integral part for the microbial inhibition of synthetic potable water containers requires investigations of the corrosion mechanism. Even though there were diversified ex-situ investigations of the tarnishing process of pure silver there is still a lack of the detailed knowledge of the reaction mechanism taking place during weathering with or without acidifying gases such as SO2, OCS or NOx. As could be shown in previous studies on copper and its alloys there is a discrepancy of the results obtained by in-situ methods to those used for the identification of the corrosion products ex-situ. The project aim is to clarify the exact mechanism of the silver oxidation and sulfidation by atmospheric pollutants such as SO2, NO2, and H2S in dependence of the humidity content of the surrounding atmosphere as well as the influence of alloy constituents such as gold. The influence of other oxidation parameters such as UV-light shall also be clarified within this project.
Research Output
- 155 Citations
- 6 Publications
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2008
Title Initial oxidation of silver surfaces by S2-and S4+ species DOI 10.1016/j.corsci.2007.12.001 Type Journal Article Author Kleber C Journal Corrosion Science Pages 1112-1121 -
2007
Title In situ investigations of the interaction of small inorganic acidifying molecules in humidified air with polycrystalline metal surfaces by means of TM-AFM, IRRAS, and QCM DOI 10.1002/sia.2583 Type Journal Article Author Kleber C Journal Surface and Interface Analysis Pages 702-710 -
2007
Title In situ QCM and TM-AFM investigations of the early stages of degradation of silver and copper surfaces DOI 10.1016/j.apsusc.2006.08.005 Type Journal Article Author Kleber C Journal Applied Surface Science Pages 3712-3721 -
2007
Title TOF-SIMS investigations on weathered silver surfaces DOI 10.1007/s00216-007-1719-8 Type Journal Article Author Schnöller J Journal Analytical and Bioanalytical Chemistry Pages 1543-1549 -
2007
Title TOF-SIMS investigations on thermally treated copper–molybdenum films on a carbon substrate DOI 10.1007/s00216-007-1734-9 Type Journal Article Author Puchner S Journal Analytical and Bioanalytical Chemistry Pages 1537-1541 -
2010
Title Investigations of the interactions of CO2, O3 and UV light with silver surfaces by in situ IRRAS/QCM and ex situ TOF-SIMS DOI 10.1016/j.apsusc.2009.11.019 Type Journal Article Author Wiesinger R Journal Applied Surface Science Pages 2735-2741