Inner Mongolia Key Laboratory of Chemistry and Physics of Rare Earth Materials, College of Chemistry and Chemical Engineering, Inner Mongolia University, Hohhot 010021, China.
Inner Mongolia Key Laboratory of Chemistry and Physics of Rare Earth Materials, College of Chemistry and Chemical Engineering, Inner Mongolia University, Hohhot 010021, China.
J Colloid Interface Sci. 2023 Aug 15;644:519-532. doi: 10.1016/j.jcis.2023.03.202. Epub 2023 Apr 5.
This work reported on the development of CoFeO-BiVO photoanode based photoelectrocatalytic system collaborating with peroxymonosulfate activation for organic contaminants removal. CoFeO layer not only provided active sites for direct peroxymonosulfate activation but also accelerated charge separation process for the enhancement of photocurrent density and photoelectrocatalytic performance. Junction of CoFeO layer on BiVO photoanode led to the improvement of photocurrent density to 4.43 mA/cm at 1.23 V, which was approximately 4.06 times higher than that of pure BiVO. Subsequently, the corresponding optimal degradation efficiency toward the tetracycline model contaminant achieved to be 89.1% with total organic carbon removal value of about 43.7% within 60 min. Moreover, the degradation rate constant of CoFeO-BiVO photoanode in photoelectrocatalytic system was 0.037 min, which was about 1.23, 2.64 and 3.70 times higher than the values in photocatalysis, electrocatalysis and PMS only based systems, respectively. In addition, radical scavenging experiments and electron spin resonance spectra indicated a synergy of radical and nonradical coupling process where •OH and O played vital roles during tetracycline degradation. Plausible photoelectrocatalytic mechanism and degradation pathway were proposed. This work provided an effective strategy to construct peroxymonosulfate assisted photoelectrocatalytic system toward green environmental applications.
这项工作报道了基于 CoFeO-BiVO 光电阳极的协同过一硫酸盐活化光催化体系的开发,用于去除有机污染物。CoFeO 层不仅提供了直接过一硫酸盐活化的活性位点,而且还加速了电荷分离过程,从而提高了光电流密度和光电催化性能。CoFeO 层与 BiVO 光阳极的结合提高了光电流密度,在 1.23 V 时达到 4.43 mA/cm,约为纯 BiVO 的 4.06 倍。随后,对于四环素模型污染物,相应的最佳降解效率达到 89.1%,总有机碳去除值约为 43.7%,在 60 min 内。此外,在光电催化体系中,CoFeO-BiVO 光阳极的降解速率常数为 0.037 min,分别是光催化、电催化和仅基于过一硫酸盐体系的 1.23、2.64 和 3.70 倍。此外,自由基清除实验和电子顺磁共振谱表明,在四环素降解过程中,自由基和非自由基偶联过程存在协同作用,•OH 和 O 发挥了重要作用。提出了合理的光电催化机制和降解途径。这项工作为构建过一硫酸盐辅助光电催化体系用于绿色环境应用提供了一种有效的策略。