摘要
Photocatalytic uranium recovery from water bodies is hindered by the poor pH stability and low photocarrier separation efficiency of conventional photocatalysts. Herein, we constructed a recyclable rGO/g-C 3 N 4 aerogel with a Schottky junction that simultaneously addressed both limitations. The optimized rGO/g-C 3 N 4 -2 exhibited pH-insensitive performance (pH 2.0–9.0). Furthermore, the Schottky barrier directs unidirectional electron migration toward rGO under illumination, boosting charge separation efficiency to 78.5%. These Schottky-junction-enabled charge dynamics, large specific surface area, the layered structure that facilitated mass and electron transport, and the favorable negative surface charge for UO 2 2+ enrichment collectively contributed to the photocatalytic performance. Consequently, rGO/g-C 3 N 4 -2 demonstrated a 92.9% uranium extraction efficiency within 120 min and maintained high efficiency even after 5 cycles under visible light. DFT calculations revealed band gap narrowing to 1.65 eV (vs 2.20 eV for pristine g-C 3 N 4 ), thereby increasing the light utilization rate. In situ DRIFTS spectroscopy revealed the evolution pathway of active species from • O 2 – to H 2 O 2 . Combined with XPS and XRD analysis, the transformation of U(VI) into (UO 2 )O 2 ·2H 2 O after photocatalytic uranium extraction was confirmed. This study presents a pH-tolerant and recyclable photocatalyst with a Schottky junction for uranium extraction from complex aqueous environments, offering a viable strategy for sustainable nuclear fuel cycles.
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