利用新型 Z 型 Zn0.5Ni0.5Fe2O4/SiNWs 异质结构协同光电催化降解四环素:实现可持续的抗生素修复

EcoEnergy Pub Date : 2024-07-10 DOI:10.1002/ece2.54
Yang Dong, Bo Wang, Dongzhou Xie, Jun Lv, Jiewu Cui, Zhiyong Bao, Guangqing Xu, Wangqiang Shen
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引用次数: 0

摘要

光电催化技术(PEC)是一种处理抗生素废水的新兴绿色可持续技术。然而,光生载流子的重组限制了该技术的有效性。为解决这一问题,可将高级氧化过程芬顿反应与 PEC 技术相结合,以增强抗生素废水的氧化降解能力。这项研究通过旋涂技术制造出 Zn0.5Ni0.5Fe2O4/硅纳米线(SiNWs)Z 型异质结,然后将其用于 PEC 耦合芬顿反应,以分解抗生素废水。固有的电场和施加的电压加速了系统内 e- 和 h+ 的分离。这些优点使得 Zn0.5Ni0.5Fe2O4/SiNWs 异质结在去除四环素(TC)、环丙沙星(CIP)、阿莫西林(AMX)和左氧氟沙星(LVX)等多种抗生素方面具有很高的效率。其中,Zn0.5Ni0.5Fe2O4/SiNWs 异质结对 TC 的降解效率为 82.21%,动力学常数(k)为 0.02688 min-1,是 SiNWs 的 2.82 倍(4.80 倍)。实验结果表明,Zn0.5Ni0.5Fe2O4/SiNWs 具有优异的光吸收特性,并降低了光生电荷重组的速率。Zn0.5Ni0.5Fe2O4 的掺杂有效提高了 SiNWs 的催化性能。这项研究为研究用于降解抗生素的 PEC 耦合 Fenton 反应方法提供了新的见解,并为今后创造更有效的光电化学催化剂铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Synergistic photoelectrocatalytic degradation of tetracycline using a novel Z-scheme Zn0.5Ni0.5Fe2O4/SiNWs heterostructure: Towards sustainable antibiotic remediation

Synergistic photoelectrocatalytic degradation of tetracycline using a novel Z-scheme Zn0.5Ni0.5Fe2O4/SiNWs heterostructure: Towards sustainable antibiotic remediation

Photoelectrocatalytic 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.

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