Electrochemical extraction of uranium from seawater is a promising strategy for the sustainable supply of nuclear fuel, whereas the current progress suffers from the co-deposition of impurities. Herein, we construct a synergistic coordination-reduction interface in CMOS@NSF, achieving electrochemical extraction of black UO product from seawater. The internal sulfur of CoMoOS tailors the electron distribution, resulting in the electron accumulation of terminal O sites for strong uranyl binding. Meanwhile, the interfacial connection of CoMoOS with NiS accelerates the electron transfer and promoted the reductive properties. Such synergistic coordination-reduction interface ensures the formation and preservation of tetravalent uranium, preventing the co-deposition of alkalis in crystalline transformation. From natural seawater, CMOS@NSF exhibits an electrochemical extraction capacity of 2.65 mg g d with black UO solid products as final products. This work provides an efficient strategy for the electrochemical uranium extraction from seawater with low impurities.
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http://dx.doi.org/10.1038/s41467-025-57113-0 | DOI Listing |
Nat Commun
February 2025
State Key Laboratory of Environment-friendly Energy Materials, School of National Defense & Nuclear Science and Technology, School of Materials & Chemistry, CAEA Innovation Center of Nuclear Environmental Safety Technology, Southwest University of Science & Technology, Mianyang, PR China.
Electrochemical extraction of uranium from seawater is a promising strategy for the sustainable supply of nuclear fuel, whereas the current progress suffers from the co-deposition of impurities. Herein, we construct a synergistic coordination-reduction interface in CMOS@NSF, achieving electrochemical extraction of black UO product from seawater. The internal sulfur of CoMoOS tailors the electron distribution, resulting in the electron accumulation of terminal O sites for strong uranyl binding.
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