TY - JOUR
T1 - Z-scheme heterojunction photocatalyst of LaFeO3@CoS for tetracycline hydrochloride degradation by persulfate activation using visible light
AU - Zhan, Jiayu
AU - Liang, Liping
AU - Lu, Ying
AU - Jiang, Shanping
AU - Imanova, Gunel
AU - Komarneni, Sridhar
AU - Ma, Jianfeng
N1 - Publisher Copyright:
© 2024 Elsevier Ltd and Techna Group S.r.l.
PY - 2025/1
Y1 - 2025/1
N2 - An efficient and stable LaFeO3@CoS Z-scheme heterojunction photocatalyst was prepared through the hydrothermal method (HT). Photocatalytic activity of the LaFeO3@CoS was assessed by activating persulfate under visible light for the degradation of tetracycline (0.1 g/L). Under the condition of 0.06 g/L of KHSO5 (Peroxymonosulfate, PMS), the degradation efficiency of 88.7 % was achieved in 40 min using the 0.02 g/L of developed photocatalyst. The degradation kinetic constants of LaFeO3@CoS were 2.79 and 2.23 times higher than those of LaFeO3 and CoS, respectively. Furthermore, the catalyst exhibited excellent stability over five consecutive degradation cycles. Possible degradation mechanisms and the electron transfer mechanism of the heterojunction formed by the LaFeO3@CoS were investigated by quenching experiments, nitrogen N₂ purging experiments, electron spin resonance (ESR) measurements and corresponding electrochemical analyses. In the LaFeO3@CoS/Vis/PMS system, the Z-scheme charge transfer pathway not only accelerated charge transport efficiency but also effectively spatially separated electrons and holes, enhancing the photocatalytic performance of the photocatalyst. Additionally, the generation of reactive species such as 1O2, O2• −, and SO4• − significantly contributed to the improved degradation efficiency of the present catalyst during the degradation process.
AB - An efficient and stable LaFeO3@CoS Z-scheme heterojunction photocatalyst was prepared through the hydrothermal method (HT). Photocatalytic activity of the LaFeO3@CoS was assessed by activating persulfate under visible light for the degradation of tetracycline (0.1 g/L). Under the condition of 0.06 g/L of KHSO5 (Peroxymonosulfate, PMS), the degradation efficiency of 88.7 % was achieved in 40 min using the 0.02 g/L of developed photocatalyst. The degradation kinetic constants of LaFeO3@CoS were 2.79 and 2.23 times higher than those of LaFeO3 and CoS, respectively. Furthermore, the catalyst exhibited excellent stability over five consecutive degradation cycles. Possible degradation mechanisms and the electron transfer mechanism of the heterojunction formed by the LaFeO3@CoS were investigated by quenching experiments, nitrogen N₂ purging experiments, electron spin resonance (ESR) measurements and corresponding electrochemical analyses. In the LaFeO3@CoS/Vis/PMS system, the Z-scheme charge transfer pathway not only accelerated charge transport efficiency but also effectively spatially separated electrons and holes, enhancing the photocatalytic performance of the photocatalyst. Additionally, the generation of reactive species such as 1O2, O2• −, and SO4• − significantly contributed to the improved degradation efficiency of the present catalyst during the degradation process.
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U2 - 10.1016/j.ceramint.2024.11.090
DO - 10.1016/j.ceramint.2024.11.090
M3 - Article
AN - SCOPUS:85208770101
SN - 0272-8842
VL - 51
SP - 1081
EP - 1095
JO - Ceramics International
JF - Ceramics International
IS - 1
ER -