Enhanced photocatalytic degradation of organic contaminants over CaFe2O4 under visible LED light irradiation mediated by peroxymonosulfate

A simple sol-gel approach is proposed herein to fabricate CaFe2O4 for the degradation of various organic pollutants (rhodamine B (RhB), tetracycline hydrochloride, humic acid, and methylene orange) under LED light irradiation mediated by peroxymonosulfate (PMS). The results indicate that the calcination temperature can significantly influence the performance of CaFe2O4 for PMS activation, and the CaFe2 04 sample obtained at 800 degrees C (CaFe2O4-800) exhibits the best efficiency in degrading RhB, which is much higher than that of Fez 03 -800. This can be attributed to the efficient separation of photogenerated electrons (e(-)) and holes (h(+)) by PMS, which is validated by transient photocurrent response and photoluminescence measurements. Results from density functional theory calculations indicate that the valence band of CaFe2O4-800 exhibits a high concentration of carriers and weak localization of electrons, which are favorable for PMS activation. Radical scavenging results confirm that h(+) and O-2(center dot-) are the dominant reactive species. Moreover, CaFe2O4-800 not only demonstrated a stable performance during eight cycling runs with negligible iron leaching but also exhibited excellent degradation efficiency under natural water and sunlight. Finally, the mechanism and pathway of RhB degradation by theCaFe(2)O(4)-800/PMS/LED system are also proposed. This work presents the enormous prospect of CaFe2O4 as an environmentally benign photocatalyst for PMS activation. (C) 2020 Published by Elsevier Ltd on behalf of The editorial office of Journal of Materials Science & Technology.

Automated summary

A simple sol-gel method was used to fabricate CaFe2O4 for efficient degradation of various organic pollutants under LED light irradiation mediated by peroxymonosulfate (PMS). Results showed that CaFe2O4-800 exhibited the best efficiency in degrading RhB, attributed to efficient charge separation and high carrier concentration. The photocatalyst also demonstrated stable performance and excellent degradation efficiency under natural conditions, indicating its potential as an environmentally friendly photocatalyst for PMS activation.