Abstract
Organic pollutants present a substantial risk to both ecological systems and human well-being. Activation of peroxymonosulfate (PMS) have emerged as an effective strategy for the degradation of organic pollutants. Bi-based heterojunction is commonly used as a photocatalyst for reductively activating PMS, but single-component Bi-based heterojunction frequently underperforms due to its restricted absorption spectrum and rapid combination of photogenerated electron-hole pairs. Herein, BiVO(4) was selected as the oxidative semiconductor to form an S-type heterojunction with CuBi(2)O(4)-x-CuBi(2)O(4)/BiVO(4) (x = 0.2, 0.5, and 0.8) for PMS photoactivation. The built-in electric field (BEF) in x-CuBi(2)O(4)/BiVO(4) promoted electron transfer to effectively activate PMS. The x-CuBi(2)O(4)/BiVO(4) heterojunctions also demonstrate stronger adsorption of the polar PMS than pure CuBi(2)O(4) or BiVO(4). In addition, the BEF prompts photoelectrons able to reduce O(2) to •O(2)(-) and photogenerated holes in the valence band of BiVO(4) able to oxidize H(2)O to generate •OH. Therefore, under visible light irradiation, 95.1% of ciprofloxacin (CIP) can be degraded. The 0.5-CuBi(2)O(4)/BiVO(4) demonstrated the best degradation efficiency and excellent stability in cyclic tests, as well as a broad applicability in degrading other common pollutants. The present work demonstrates the high-efficiency S-type heterojunctions in the coupled photocatalytic and PMS activation technology.