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Published on: August 23, 2012
Schottky-Junction-Driven Charge Separation in a 3D rGO/g-C3N4 Aerogel for pH-Tolerant Photocatalytic Uranium
Zhiyao Wu1, Yuxiang Deng2, Zi Yang3
1State Key Laboratory of Chemistry for NBC Hazards Protection, Frontiers Science Center for Rare Isotopes, School of Nuclear Science and Technology, Lanzhou University, Lanzhou730000, China.
Abstract:
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-C3N4 aerogel with a Schottky junction that simultaneously addressed both limitations. The optimized rGO/g-C3N4-2 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 UO22+ enrichment collectively contributed to the photocatalytic performance. Consequently, rGO/g-C3N4-2 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-C3N4), thereby increasing the light utilization rate. In situ DRIFTS spectroscopy revealed the evolution pathway of active species from •O2- to H2O2. Combined with XPS and XRD analysis, the transformation of U(VI) into (UO2)O2·2H2O 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.
