光催化
水溶液
异质结
材料科学
阳极
化学工程
电化学
阳极氧化
锐钛矿
纳米颗粒
二氧化钛
纳米管
可见光谱
钛
电极
纳米技术
无机化学
催化作用
化学
碳纳米管
光电子学
物理化学
工程类
冶金
铝
生物化学
作者
Wenlan Ji,Yuan Wang,Tian Cheng Zhang,Like Ouyang,Shaojun Yuan
标识
DOI:10.1021/acs.iecr.1c03420
摘要
Addressing the ever-growing arsenite pollution in groundwater has become an essential and urgent issue for ensuring the safety of human beings and the environment. It is highly attractive to preoxidize As(III) to relatively low toxic As(V) for further efficient arsenic removal by adsorption, ion exchange, or coagulation. In this study, a novel heterostructure Cu2O@TiO2 nanotube array coated titanium anode (CTNTA) was fabricated by combination of electrochemical anodization and electrodeposition and used for the highly efficient photoelectrocatalytic oxidation conversion of As(III) to As(V) in aqueous solution. The morphology, composition, and photoelectric performances of the CTNTA anode were systematically characterized. The effect of the loading amount of Cu2O nanoparticles on the photoelectrocatalytic oxidation kinetics of As(III) was investigated, and the comparison study among photocatalytic, electrocatalytic, and photoelectrocatalytic oxidations of As(III) was also explored to demonstrate the synergistic effect of As(III) oxidation conversion performance. The heterostructure CTNTAs-1.00 delivered a substantially enhanced photoelectrocatalytic oxidation ratio of As(III) at 95% within 30 min at a current density of 10 mA·cm–2 under visible-light irradiation. The electrochemical deposition amount of Cu2O nanoparticles on TiO2 nanotube arrays (TNTAs) was found to be positively correlated with the achievement of boosted As(III) oxidation efficiency. The high photoelectrocatalytic oxidation performance of the CTNTA was ascribed to the favored separation efficiency of photoinduced carriers and electron–hole pairs under both visible light irradiation and electric potential conditions. The photoelectrocatalytic oxidation reaction mechanism was proven to be ascribed to the active species of holes (h+), superoxide radicals (•O2–), and hydroxyl radicals (•OH). These results highlight the high conversion rate of As(III) by the photoelectrocatalytic oxidation reaction on such a nanostructured anode, which offers a promising methodology for further in-depth oxidation of As(III) in aqueous solution.
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