TY - JOUR
T1 - Degradation of metronidazole by activating peroxymonosulfate using Z-scheme heterojunction photocatalysts of Co3O4/NiCo2O4 double shell nanocages under visible light
AU - Mei, Dong
AU - Lu, Songhua
AU - Liang, Liping
AU - Komarneni, Sridhar
AU - Ma, Jianfeng
N1 - Publisher Copyright:
© 2025 Elsevier B.V.
PY - 2025/8/20
Y1 - 2025/8/20
N2 - In this study, ZIF-67 derived Co3O4/NiCo2O4 double shell nanocages (DSNCs) were fabricated and utilized to degrade metronidazole (MNZ) by activating peroxymonosulfate (PMS) under visible light. The Co3O4/NiCo2O4-3 (C/N-3) degrade 99.9 % of MNZ by activating PMS under visible light within 20 min, which showed excellent catalytic performance. The double shell nanocage structure effectively reduces the penetration loss of incident light, and the multiple refractions inside the shell effectively enhance the light trapping ability. C/N-3 demonstrates enhanced light absorption capacity, facilitating increased excitation of ground-state electrons to improve catalytic efficiency. Additionally, C/N-3 degrade MNZ well across a wide pH range (3−11) by activating PMS under visible light. The degradation kinetic constant of 0.234 min−1 for the C/N-3/PMS/Vis system was 29.25 and 2.21 times higher than those of Co3O4 and NiCo2O4, respectively. Furthermore, C/N-3 showed excellent stability through five successive degradation cycle experiments (more than 85.3 %). In summary, the C/N-3 photocatalysts provide valuable insights into water pollution treatment by activating PMS under visible light.
AB - In this study, ZIF-67 derived Co3O4/NiCo2O4 double shell nanocages (DSNCs) were fabricated and utilized to degrade metronidazole (MNZ) by activating peroxymonosulfate (PMS) under visible light. The Co3O4/NiCo2O4-3 (C/N-3) degrade 99.9 % of MNZ by activating PMS under visible light within 20 min, which showed excellent catalytic performance. The double shell nanocage structure effectively reduces the penetration loss of incident light, and the multiple refractions inside the shell effectively enhance the light trapping ability. C/N-3 demonstrates enhanced light absorption capacity, facilitating increased excitation of ground-state electrons to improve catalytic efficiency. Additionally, C/N-3 degrade MNZ well across a wide pH range (3−11) by activating PMS under visible light. The degradation kinetic constant of 0.234 min−1 for the C/N-3/PMS/Vis system was 29.25 and 2.21 times higher than those of Co3O4 and NiCo2O4, respectively. Furthermore, C/N-3 showed excellent stability through five successive degradation cycle experiments (more than 85.3 %). In summary, the C/N-3 photocatalysts provide valuable insights into water pollution treatment by activating PMS under visible light.
UR - https://www.scopus.com/pages/publications/105012718609
UR - https://www.scopus.com/inward/citedby.url?scp=105012718609&partnerID=8YFLogxK
U2 - 10.1016/j.jallcom.2025.182879
DO - 10.1016/j.jallcom.2025.182879
M3 - Article
AN - SCOPUS:105012718609
SN - 0925-8388
VL - 1038
JO - Journal of Alloys and Compounds
JF - Journal of Alloys and Compounds
M1 - 182879
ER -