Issue 6, 2018

Preparation of magnetically separable and recyclable carbon dots/NiCo2O4 composites with enhanced photocatalytic activity for the degradation of tetracycline under visible light

Abstract

Utilizing photocatalysis to remove antibiotics from aqueous solution is a promising technology for environmental remediation. In this work, we successfully fabricated a visible-light-responsive and magnetically recycled carbon dot (CD)/NiCo2O4 composite photocatalyst through a one-step simple calcination method for the first time. Compared with pristine NiCo2O4, CDs/NiCo2O4 composites exhibit significantly enhanced photocatalytic activity for the degradation of tetracycline (TC) (100 mL, 10 mg L−1) under visible-light irradiation. The photodegradation rate constant data reveal that CDs/NiCo2O4 with 3 wt% CD loading content (CDs/NiCO-3) exhibited the highest photocatalytic activity (0.02134 min−1), which is about 6-fold in comparison with pristine NiCo2O4 (0.0036 min−1). The enhanced photocatalytic activity of the CDs/NiCo2O4 composite corresponds to the synergetic effect of CDs and NiCo2O4 that improves not only the light absorption capacity but also the separation efficiency of photo-induced charge carriers. Additionally, the CDs/NiCo2O4 composites showed good recyclability without loss of apparent photocatalytic activity after five successive cycles, and more importantly, CDs/NiCo2O4 could be recovered magnetically.

Graphical abstract: Preparation of magnetically separable and recyclable carbon dots/NiCo2O4 composites with enhanced photocatalytic activity for the degradation of tetracycline under visible light

Supplementary files

Article information

Article type
Research Article
Submitted
30 Mar 2018
Accepted
15 Apr 2018
First published
20 Apr 2018

Inorg. Chem. Front., 2018,5, 1438-1444

Preparation of magnetically separable and recyclable carbon dots/NiCo2O4 composites with enhanced photocatalytic activity for the degradation of tetracycline under visible light

J. Jiang, W. Shi, F. Guo and S. Yuan, Inorg. Chem. Front., 2018, 5, 1438 DOI: 10.1039/C8QI00290H

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