Insights into Photothermally Enhanced Photocatalytic U(VI) Extraction by a Step-Scheme Heterojunction

In this work, a CdS/BiVO4 step-scheme (S-scheme) heterojunction with self-photothermally enhanced photocatalytic effect was synthesized and applied for efficient U(VI) photoextraction. Characterizations such as transient absorption spectroscopy and Tafel test together confirmed the formation of S-scheme heterojunctions, which allows CdS/BiVO4 to avoid photocorrosion while retaining the strong reducing capacity of CdS and the oxidizing capacity of BiVO4. Experimental results such as radical quenching experiments and electron spin resonance show that U(VI) is rapidly oxidized by photoholes/center dot OH to insoluble UO2(OH)2 after being reduced to U(IV) by photoelectrons/center dot O2-, which precisely avoids the depletion of electron sacrificial agents. The rapid recombination of electron-hole pairs triggered by the S-scheme heterojunction is found to release large amounts of heat and accelerate the photocatalysis. This work offers a new enhanced strategy for photocatalytic uranium extraction and presents a direction for the design and development of new photocatalysts.

Automated summary

This study synthesized a CdS/BiVO4 step-scheme (S-scheme) heterojunction with self-photothermally enhanced photocatalytic effect for efficient U(VI) photoextraction. Experimental results showed that the S-scheme heterojunction allowed rapid oxidation of U(VI) while avoiding the depletion of electron sacrificial agents. The rapid recombination of electron-hole pairs triggered by the heterojunction released large amounts of heat and accelerated the photocatalysis. This work provides a new enhanced strategy for photocatalytic uranium extraction and presents a direction for the design and development of new photocatalysts.