Electrodeposition of Ti in molten AF–ACl–A<sub>3</sub>TiF<sub>6</sub> (A = Li, Na, K)

Electrochemical behaviors of Ti(III) ions and electrodeposition of Ti were investigated in molten AF–ACl–A 3 TiF 6 (A = Li, Na, K) at 973 K. Redox currents corresponding to Ti(III)/Ti(0) and Ti(IV)/Ti(III) reactions were observed by cyclic voltammetry. The redox potentials of the reactions with reference to Cl 2 /Cl − and F 2 /F − were most positive for the Li system, followed by the Na system, and most negative for the K system. The differences in the potential can be explained by the interactions of alkali cations and F - ions; smaller cations interact more strongly with F − , resulting in a weaker interaction between Ti(III) ions and F - ions. As a result, the electrochemical stability of TiF 6 3− decreased. The electrodeposited Ti was confirmed to be crystalline by XRD, and the orientation of the Ti crystals differed depending on the molten salt.

Authors

Publication Details

Journal
ECS Transactions
Published
2024-09-27
DOI
https://doi.org/10.1149/11406.0023ecst
Citations
1
Primary Topic
Metallurgical and Alloy Processes
Type
article
Field-Weighted Citation Impact
1.47
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article

Electrodeposition of Ti in molten AF–ACl–A3TiF6 (A = Li, Na, K)

Toshiyuki Nohira, Yutaro Norikawa
1 citations
ECS Transactions
Metallurgical and Alloy Processes
1.47
article

Electrodeposition of Ti in molten AF–ACl–A3TiF6 (A = Li, Na, K)

Toshiyuki Nohira, Yutaro Norikawa
article en
1 citations

Abstract

Electrochemical behaviors of Ti(III) ions and electrodeposition of Ti were investigated in molten AF–ACl–A 3 TiF 6 (A = Li, Na, K) at 973 K. Redox currents corresponding to Ti(III)/Ti(0) and Ti(IV)/Ti(III) reactions were observed by cyclic voltammetry. The redox potentials of the reactions with reference to Cl 2 /Cl − and F 2 /F − were most positive for the Li system, followed by the Na system, and most negative for the K system. The differences in the potential can be explained by the interactions of alkali cations and F - ions; smaller cations interact more strongly with F − , resulting in a weaker interaction between Ti(III) ions and F - ions. As a result, the electrochemical stability of TiF 6 3− decreased. The electrodeposited Ti was confirmed to be crystalline by XRD, and the orientation of the Ti crystals differed depending on the molten salt.

ECS TransactionsVol. 114(6)
Openalex Percentile: Top 15%
Metallurgical and Alloy Processes
1.47
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