Negatively Charged Catalytic Centers on MXene for Sustainable Uranium Recovery

Efficient and selective uranium extraction from wastewater remains a significant challenge, primarily because conventional adsorbents exhibit low affinity for UO 2 2+, while most catalytic centers are either neutral or positively charged, creating a fundamental charge incompatibility with the target ions. To overcome this, we adopted an integrated adsorption–electrocatalysis strategy using a freestanding membrane electrode (ZMOM), fabricated via electrostatic self-assembly of Ti 3 C 2 T x MXene and zinc molybdate (ZMO). The key innovation lies in employing molybdate ions as bifunctional units that combine a negatively charged surface for electrostatic attraction of UO 2 2+ with oxygen-bridged configurations that serves as integrated catalytic sites. This synergy enables continuous capture and molybdenum-mediated redox conversion (U 6+ ↔ U 5+ ), leading to the precipitation of insoluble Na 2 O(UO 3 ·H 2 O) x for easy recovery. Under the square-wave exchange (SWE) method, the optimized ZMOM-2 electrode achieves a high uranium extraction capacity of 1641.78 mg/g at −5 V from a 100 mg/L solution and retains 98.78% of its capacity over five consecutive cycles. This work establishes a new design principle that integrates adsorption sites and anionic catalytic centers into a single material, offering an efficient and robust route for uranium resource recovery.