Electrowinning for Room-Temperature Ironmaking: Mapping the Electrochemical Aqueous Iron Interface

A promising route toward room-temperature ironmaking is electrowinning, where iron ore dissolution is coupled with cation electrodeposition to grow pure iron. However, poor faradaic efficiencies against the hydrogen evolution reaction (HER) is a major bottleneck. To develop a mechanistic picture of this technology, we conduct a first-principles thermodynamic analysis of the Fe110 aqueous electrochemical interface. Constructing a surface Pourbaix diagram, we predict that the iron surface will always drive toward adsorbate coverage. We calculate theoretical overpotentials for terrace and step sites and predict that growth at the step sites are likely to dominate. Investigating the hydrogen surface phases, we model several hydrogen absorption mechanisms, all of which are predicted to be endothermic. Additionally, for HER we identify step sites as being more reactive than on the terrace and with competitive limiting potentials to iron plating. The results presented here further motivate electrolyte design toward HER suppression.

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Publication Details

Journal
The Journal of Physical Chemistry C
Published
2024-08-22
DOI
https://doi.org/10.1021/acs.jpcc.4c01867
Citations
8
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
0.82

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article

Electrowinning for Room-Temperature Ironmaking: Mapping the Electrochemical Aqueous Iron Interface

Venkatasubramanian Viswanathan, Lance Kavalsky
8 citations
The Journal of Physical Chemistry C
Electrocatalysts for Energy Conversion
0.82
article

Electrowinning for Room-Temperature Ironmaking: Mapping the Electrochemical Aqueous Iron Interface

Venkatasubramanian Viswanathan, Lance Kavalsky
article en
8 citations

Abstract

A promising route toward room-temperature ironmaking is electrowinning, where iron ore dissolution is coupled with cation electrodeposition to grow pure iron. However, poor faradaic efficiencies against the hydrogen evolution reaction (HER) is a major bottleneck. To develop a mechanistic picture of this technology, we conduct a first-principles thermodynamic analysis of the Fe110 aqueous electrochemical interface. Constructing a surface Pourbaix diagram, we predict that the iron surface will always drive toward adsorbate coverage. We calculate theoretical overpotentials for terrace and step sites and predict that growth at the step sites are likely to dominate. Investigating the hydrogen surface phases, we model several hydrogen absorption mechanisms, all of which are predicted to be endothermic. Additionally, for HER we identify step sites as being more reactive than on the terrace and with competitive limiting potentials to iron plating. The results presented here further motivate electrolyte design toward HER suppression.

The Journal of Physical Chemistry CVol. 128(35)
University of Michigan (US), Carnegie Mellon University (US)
Natural Sciences and Engineering Research Council of Canada
Openalex Percentile: Top 33%
Electrocatalysts for Energy Conversion
0.82
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