期刊
ACS SUSTAINABLE CHEMISTRY & ENGINEERING
卷 9, 期 43, 页码 14631-14643出版社
AMER CHEMICAL SOC
DOI: 10.1021/acssuschemeng.1c06189
关键词
dysprosium; electrodeposition; ionic liquid; water; speciation heterogeneity; reduction mechanism; interfacial processes; metal stability and purity
资金
- US Department of Energy through the Critical Materials Institute
- INL under DOE Idaho Operations Office Contract [DE AC07 05ID14517]
The study conducted a comprehensive investigation on the influence of water on dysprosium electrodeposition in an ionic liquid and found that water introduction has multiple impacts on various aspects of the deposition process, such as reduction pathways, coordination, and nucleation. While water introduction improved reduction rates and Faradaic efficiency, it also led to instability and limited purity of the deposited dysprosium metal. High water content also triggered a hydrogen evolution reaction, affecting system efficiency.
The electrochemical production of rare earth metals (REMs) in ionic liquids (ILs) has received much attention as a promising, sustainable replacement to molten salt electrolysis. Water additives have been suggested as a promoting strategy for the ionic liquid process; however, the fundamental understanding of the interfacial processes required to assess the overall viability for REM production is lacking. In this regard, a full investigation of the impact of water on dysprosium (Dy) electrodeposition in pyrrolidinium triflate (BMPyOTf) ionic liquid was carried out. Water introduction was revealed to involve an interplay of implications on the electrodeposition process, including coordination, speciation, reduction pathways, interfacial dynamics, nucleation, and metal stability and purity. Under highly dry conditions, the reduction occurs at a very negative potential (-3.3 V) in a consecutive pathway, resulting in negligible metal electrodeposition (low rate and efficiency) at the electrode surface. Small water concentrations (<500 ppm) lead to partitioning of the Dy complex between water and IL-coordinated speciation, giving rise to an additional wave at a more positive potential (-2.4 V). Probing the heterogeneous Dy speciation by spectroscopic analyses enabled uncovering of the reduction mechanism and evaluation of the mass transport properties. In addition to lowering the reduction thermodynamics, water introduction also improved the nucleation, deposition rate, and faradic efficiency. Despite these benefits, stripping voltammetric analysis predicts substantial chemical reactivity of the deposited Dy metal with water additives and/or electrolyte components, under long timescales. Surface characterization of the obtained product confirmed the instability of Dy metal as an oxidized/fluorinated material and its limited purity (similar to 60%). Moreover, high water introduction triggered a fast hydrogen evolution reaction (HER), downgrading the robustness of system efficiency. The overall impact of water additives seems to engender both promoting and mitigating effects on electrochemical REM production in IL, requiring a specific technoeconomic assessment and/or more innovative strategies to be sought.
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