“Ion-imprinting” strategy towards metal sulfide scavenger enables the highly selective capture of radiocesium

Abstract Highly selective capture of radiocesium is an urgent need for environmental radioactive contamination remediation and spent fuel disposal. Herein, a strategy is proposed for construction of “inorganic ion-imprinted adsorbents” with ion recognition-separation capabilities, and a metal sulfide Cs 2.33 Ga 2.33 Sn 1.67 S 8 ·H 2 O (FJSM-CGTS) with “imprinting effect” on Cs + is prepared. We show that the K + activation product of FJSM-CGTS, Cs 0.51 K 1.82 Ga 2.33 Sn 1.67 S 8 ·H 2 O (FJMS-KCGTS), can reach adsorption equilibrium for Cs + within 5 min, with a maximum adsorption capacity of 246.65 mg·g −1 . FJMS-KCGTS overcomes the hindrance of Cs + adsorption by competing ions and realizes highly selective capture of Cs + in complex environments. It shows successful cleanup for actual 137 Cs-liquid-wastes generated during industrial production with removal rates of over 99%. Ion-exchange column filled with FJMS-KCGTS can efficiently treat 540 mL Cs + -containing solutions (31.995 mg·L −1 ) and generates only 0.12 mL of solid waste, which enables waste solution volume reduction. Single-crystal structural analysis and density functional theory calculations are used to visualize the “ion-imprinting” process and confirm that the “imprinting effect” originates from the spatially confined effect of the framework. This work clearly reveals radiocesium capture mechanism and structure-function relationships that could inspire the development of efficient inorganic adsorbents for selective recognition and separation of key radionuclides.