Affiliation:
1. School of Materials Science and Engineering Hefei University of Technology Hefei China
2. National Laboratory of Solid State Microstructures and Department of Physics Nanjing University Nanjing China
3. Key Laboratory of Advanced Functional Materials and Devices of Anhui Province Hefei University of Technology Hefei China
4. State Key Laboratory of Structural Chemistry Fujian Institute of Research on the Structure of Matter Chinese Academy of Sciences Fuzhou China
Abstract
AbstractPhotoelectrocatalytic technology (PEC) is an emerging green and sustainable technology for treating antibiotic wastewater. However, its effectiveness is limited by the recombination of photogenerated carriers. To address this issue, the Fenton reaction, an advanced oxidation process, can be coupled with PEC technology to enhance the oxidative degradation of antibiotic wastewater. This research involved creating a Zn0.5Ni0.5Fe2O4/silicon nanowires (SiNWs) Z‐type heterojunction through the spin coating technique, which was then utilized in the PEC coupled Fenton reaction to break down antibiotic wastewater. The inherent electric field and the voltage applied hastened the segregation of e− and h+ within the system. These advantages make the Zn0.5Ni0.5Fe2O4/SiNWs heterojunction highly efficient in removing various antibiotics, including tetracycline (TC), ciprofloxacin (CIP), amoxicillin (AMX), and levofloxacin (LVX). In particular, the Zn0.5Ni0.5Fe2O4/SiNWs heterojunction demonstrated an 82.21% degradation efficiency for TC, exhibiting a kinetic constant (k) of 0.02688 min−1, a rate 2.82 times (4.80 times) greater than that of SiNWs. Experimental findings reveal that Zn0.5Ni0.5Fe2O4/SiNWs exhibit superior light absorption properties and a reduced rate of photogenerated charge recombination. The doping of Zn0.5Ni0.5Fe2O4 effectively improves the catalytic performance of SiNWs. This research offers fresh insights into researching PEC‐coupled Fenton reaction methods for the degradation of antibiotics and paves the way for advancing the creation of more potent photoelectrochemical catalysts in the future.
Funder
National Natural Science Foundation of China
Cited by
1 articles.
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