Spectroscopic Study into Lanthanide Speciation in Deep Eutectic Solvents

• Published in: ACS omega 2022-01, Vol.7 (1), p.921-932
• Main Authors: Amphlett, James T. M, Lee, Yunu, Yang, Wonseok, Kang, Dokyu, Sung, Nark-Eon, Park, Jaeyeong, Jung, Euo Chang, Choi, Sungyeol
• Format: Article
• Language: English
• ISSN: 2470-1343; 2470-1343
• DOI: 10.1021/acsomega.1c05386

Deep eutectic solvents are a new class of green solvents that are being explored as an alternative for used nuclear fuel and critical material recycling. However, there is a paucity of knowledge regarding metal behavior in them. This paper explores the underlying chemistry of rare-earth elements in choline chloride-based deep eutectic solvents by using a multi-technique spectroscopic methodology. Results show that speciation is highly dependent on the choice of the hydrogen-bond donor. Collected EXAFS data showed Ln3+ coordination with ethylene glycol and urea in their respective solvents and coordination with chloride in the lactic acid system. Generalized coordination environments were determined to be [LnL4–5], [LnL7–10], and [LnL5–6] in the ethylene glycol, urea, and lactic acid systems, respectively. Collected UV/vis spectra for Nd3+ and Er3+ showed variations with changing solvents, showing that Ln–Cl interactions do not dominate in these systems. Luminescence studies were consistent, showing varying emission spectra with varying solvent systems. The shortest luminescent lifetimes were observed in the choline chloride–ethylene glycol deep eutectic solvent, suggesting coordination through O–H groups. Combining all collected data allowed Eu3+ coordination geometries to be assigned.