Enhancing radiostrontium uptake by a layered titanate perovskite via sustainable electrochemically switched ion exchange.
basic_science · Level V
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- Record sourced from PubMed, PMID 41145503.
- Also identified by DOI 10.1038/s41467-025-64537-1 and PMC identifier 12559193.
- Licence recorded as CC BY-NC-ND.
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Abstract
Green and sustainable <sup>90</sup>Sr uptake is urgently needed for radionuclides remediation. Herein, we propose an efficient strategy based on electrochemically switched ion exchange (ESIX) method to enhance <sup>90</sup>Sr uptake using electroactive ion exchange material. A titanate perovskite (Na<sub>2</sub>La<sub>2</sub>Ti<sub>3</sub>O<sub>10</sub>) with outstanding acid, irradiation resistance, and thermal stability can effectively capture Sr<sup>2+</sup> and achieve remediation of actual acidic <sup>90</sup>Sr-containing liquid waste (R<sup>Sr</sup> > 99%). Na<sub>2</sub>La<sub>2</sub>Ti<sub>3</sub>O<sub>10</sub> is prepared as working electrode C@NaLaTiO to enhance Sr<sup>2+</sup> uptake via ESIX. Remarkably, the Sr<sup>2+</sup> adsorption capacity increases (from 104.84 to 175.43 mg·g<sup>-1</sup>) and high selectivity for Sr<sup>2+</sup> is maintained even under strongly acidic solutions. The Sr<sup>2+</sup> adsorption-desorption can be controlled via facile potential modulation. Mechanism study indicates that efficient Sr<sup>2+</sup> capture originates from the ion exchange between Sr<sup>2+</sup> and interlayer Na<sup>+</sup> in Na<sub>2</sub>La<sub>2</sub>Ti<sub>3</sub>O<sub>10</sub> coupled with the electrochemical redox reaction between Ti<sup>4+</sup>/Ti<sup>3+</sup> and the increase in oxygen vacancy. Density functional theory calculations support that ESIX enhances Sr<sup>2+</sup> adsorption by increasing the binding energy of anionic [La<sub>2</sub>Ti<sub>3</sub>O<sub>10</sub>]<sub>n</sub><sup>2n-</sup> layers towards Sr<sup>2+</sup>. This study offers a convenient and environmentally friendly way for the efficient <sup>90</sup>Sr enrichment from radioactive waste liquids.