Electrochemical Capture and Accumulation of Uranium Using a Layered Uvanite Electrode

Abstract Extracting uranyl ions (UO22+) from uranium mining leachates can enhance national uranium security and mitigate the environmental impact of nuclear energy. Conventional techniques such as ion exchange and iron-based reductive precipitation have notable limitations. This study reports that the uvanite (U2V6O21) electrode, a layered uranium-vanadium oxide, enables potentiodynamic decoupling of UO22+ and proton intercalation/deintercalation, as well as proton-induced UO22+/UO3 precipitation and dissolution reactions. Building on a comprehensive understanding of charge-transfer and transport mechanisms, we found that potentiodynamic modulation enables selective capture of uranium species using a uvanite electrode. By allowing competing cations to deintercalate at lower potentials and preventing proton deintercalation, UO3 dissolution is inhibited, achieving a high UO3 recovery capacity of 515 mg/g at 10 times the competing cation concentration. The new electrochemistry of the uvanite electrode helps develop cost-effective, sustainable battery electrodes for critical ion extraction from water.

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Publication Details

Journal
ACS Energy Letters
Published
2026-11-04
DOI
https://doi.org/10.1021/acsenergylett.6c02821
Primary Topic
Radioactive element chemistry and processing
Type
article
Field-Weighted Citation Impact
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article

Electrochemical Capture and Accumulation of Uranium Using a Layered Uvanite Electrode

Gihan Kwon, Xiaowei Teng, Milinda Abeykoon, Lihua Zhang et al.
ACS Energy Letters
Radioactive element chemistry and processing
article

Electrochemical Capture and Accumulation of Uranium Using a Layered Uvanite Electrode

Gihan Kwon, Xiaowei Teng, Milinda Abeykoon, Lihua Zhang, Tongxin Zhou, Divakar Arumugam, Cheng-Hung Lin, Tian Wang
article en

Abstract

Abstract Extracting uranyl ions (UO22+) from uranium mining leachates can enhance national uranium security and mitigate the environmental impact of nuclear energy. Conventional techniques such as ion exchange and iron-based reductive precipitation have notable limitations. This study reports that the uvanite (U2V6O21) electrode, a layered uranium-vanadium oxide, enables potentiodynamic decoupling of UO22+ and proton intercalation/deintercalation, as well as proton-induced UO22+/UO3 precipitation and dissolution reactions. Building on a comprehensive understanding of charge-transfer and transport mechanisms, we found that potentiodynamic modulation enables selective capture of uranium species using a uvanite electrode. By allowing competing cations to deintercalate at lower potentials and preventing proton deintercalation, UO3 dissolution is inhibited, achieving a high UO3 recovery capacity of 515 mg/g at 10 times the competing cation concentration. The new electrochemistry of the uvanite electrode helps develop cost-effective, sustainable battery electrodes for critical ion extraction from water.

ACS Energy Letters
Worcester Polytechnic Institute (US), Brookhaven National Laboratory (US), National Synchrotron Light Source II (US), Center for Functional Nanomaterials (US)
Openalex Percentile: Top 29%
Radioactive element chemistry and processing
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