Facilitated Visible-Light-Driven Peroxymonosulfate Activation by a Co–Fe Layered Double Hydroxide Derived p–n Heterostructure for Sulfadiazine Degradation: Affecting Parameters, Kinetics, and Mechanistic Insights

化学 异质结 降级(电信) 复合数 氢氧化物 氧化物 光催化 载流子 化学工程 光化学 催化作用 无机化学 光电子学 复合材料 有机化学 材料科学 工程类 电信 计算机科学
作者
Upali Aparajita Mohanty,Dipti Prava Sahoo,Kundan Kumar Das,Lekha Paramanik,Kulamani Parida
出处
期刊:Inorganic Chemistry [American Chemical Society]
卷期号:63 (4): 1919-1937 被引量:7
标识
DOI:10.1021/acs.inorgchem.3c03582
摘要

The utilization of multivalence ionic metal species generated through a peroxymonosulfate (PMS)-assisted photocatalytic system is a promising platform for the selective degradation of water contaminants. However, achieving an effective electron transport and enhanced separation efficiency for these metal species is a daunting challenge. Thus, our current study addresses this challenge by using a Co–Fe-based layered-double-hydroxide template to synthesize a Co3O4/FeCo2O4 p–n heterojunction composite via a simple monosynthetic route. The resultant composite is thoroughly validated through advanced characterization techniques that efficiently activate PMS for sulfadiazine (SDZ) degradation under visible light, achieving a remarkable degradation efficiency of up to 90%. This accomplishment is attributed to factors including intimate interfacial contact, excellent light harvesting, mesoporosity, and oxygen vacancies within the composite. The formation of a distinct p–n heterojunction following the S-scheme charge dynamic significantly enhances photogenerated carrier separation and reduces charge recombination. The research delves into comprehensive investigations including degradation studies, active species trapping experiments, parameter exploration, and in-depth liquid chromatography–mass spectrometry for analysis of the degradation byproducts and pathway. Induced oxygen vacancies, strategically placed active surface sites, and mesoporosity in the Co3O4/FeCo2O4 composite synergistically boosted the sluggish PMS activation, leading to enhanced SDZ degradation. This study introduces a new perspective by demonstrating the potential of a single-material, mixed-metal oxide-based p–n heterojunction photocatalytic system following the S-scheme charge-transfer route for SDZ degradation. The findings contribute toward emphasizing the importance of tailored composite materials in tackling persistent contaminants.
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