Tantalum electrodeposition using a nanoporous anodic alumina template and a nanostructured gold/nickel-chromium glass-ceramic substrate
Loading...
Date
Authors
Šimůnková, Helena
Kolíbalová, Eva
Kalina, Lukáš
Lednický, Tomáš
Bábor, Petr
Hubálek, Jaromír
Advisor
Referee
Mark
Journal Title
Journal ISSN
Volume Title
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Altmetrics
Abstract
The electrodeposition and analysis of tantalum (Ta) nanotube arrays prepared from an ionic liquid, 1-butyl-1methylpyrrolidinium bis(trifluoro-methylsulfonyl) imide (BMP[Tf2N]), using a porous anodic alumina (PAA) template are newly presented. Free-standing and spatially separated tantalum nanotube arrays were achieved after selective etching of the PAA. The high-rate electrodeposition of the nanotube arrays took only 10 s and achieved approximately 70 atomic percent Ta metal. Superficial X-ray photoelectron spectroscopy supplemented by an argon ion etching and depth profiling has proven the presence of tantalum metal. Additionally, tantalum electrodeposition was attempted using a sputter-deposited gold coating on a planar glass-ceramic substrate as the working electrode. Pores emerged within the sputter-deposited gold layer as a side result of the Ta electrodeposition step. Nano-to submicrometer large pores were created due to a foreign element penetration into the gold and etching effect of fluorides contained in the ionic liquid solution.
The electrodeposition and analysis of tantalum (Ta) nanotube arrays prepared from an ionic liquid, 1-butyl-1methylpyrrolidinium bis(trifluoro-methylsulfonyl) imide (BMP[Tf2N]), using a porous anodic alumina (PAA) template are newly presented. Free-standing and spatially separated tantalum nanotube arrays were achieved after selective etching of the PAA. The high-rate electrodeposition of the nanotube arrays took only 10 s and achieved approximately 70 atomic percent Ta metal. Superficial X-ray photoelectron spectroscopy supplemented by an argon ion etching and depth profiling has proven the presence of tantalum metal. Additionally, tantalum electrodeposition was attempted using a sputter-deposited gold coating on a planar glass-ceramic substrate as the working electrode. Pores emerged within the sputter-deposited gold layer as a side result of the Ta electrodeposition step. Nano-to submicrometer large pores were created due to a foreign element penetration into the gold and etching effect of fluorides contained in the ionic liquid solution.
The electrodeposition and analysis of tantalum (Ta) nanotube arrays prepared from an ionic liquid, 1-butyl-1methylpyrrolidinium bis(trifluoro-methylsulfonyl) imide (BMP[Tf2N]), using a porous anodic alumina (PAA) template are newly presented. Free-standing and spatially separated tantalum nanotube arrays were achieved after selective etching of the PAA. The high-rate electrodeposition of the nanotube arrays took only 10 s and achieved approximately 70 atomic percent Ta metal. Superficial X-ray photoelectron spectroscopy supplemented by an argon ion etching and depth profiling has proven the presence of tantalum metal. Additionally, tantalum electrodeposition was attempted using a sputter-deposited gold coating on a planar glass-ceramic substrate as the working electrode. Pores emerged within the sputter-deposited gold layer as a side result of the Ta electrodeposition step. Nano-to submicrometer large pores were created due to a foreign element penetration into the gold and etching effect of fluorides contained in the ionic liquid solution.
Description
Citation
Vacuum. 2025, vol. 239, issue 1, p. 1-8.
https://www.sciencedirect.com/science/article/pii/S0042207X25004282
https://www.sciencedirect.com/science/article/pii/S0042207X25004282
Document type
Peer-reviewed
Document version
Accepted version
Date of access to the full text
2027-05-21
Language of document
en
Study field
Comittee
Date of acceptance
Defence
Result of defence
Endorsement
Review
Supplemented By
Referenced By
Creative Commons license
Except where otherwised noted, this item's license is described as Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International

0000-0003-1800-4686 