Center for Advanced Analytical Science, Guangzhou Key Laboratory of Sensing Materials & Devices, School of Chemistry and Chemical Engineering, Analytical and Testing Center, Guangzhou University, Guangzhou 510006, China.
Guangdong Provincial Key Laboratory of Psychoactive Substances Monitoring and Safety, Anti-Drug Technology Center of Guangdong Province, Guangzhou 510230, China.
Int J Environ Res Public Health. 2022 Nov 10;19(22):14770. doi: 10.3390/ijerph192214770.
Both type II and Z schemes can explain the charge transfer behavior of the heterojunction structure well, but the type of heterojunction structure formed between bismuth vanadium oxide and carbon nitride still has not been clarified. Herein, we rationally prepared bismuth vanadium oxide with {010} and {012} facets predominantly and carbon nitride as a decoration to construct a core-shell structure with bismuth vanadium oxide wrapped in carbon nitride to ensure the same photocatalytic reaction interface. Through energy band establishment and radical species investigation, both {010} and {012} facets dominated bismuth vanadium oxide/carbon nitride composites exhibit the type II heterojunction structures rather than the Z-scheme heterojunctions. Furthermore, to investigate the effect of type II heterojunction, the photocatalytic tetracycline degradations were performed, finding that {010} facets dominated bismuth vanadium oxide/carbon nitride composite demonstrated the higher degradation efficiency than that of {012} facets, due to the higher conduction band energy. Additionally, through the free radical trapping experiments and intermediate detection of degradation products, the superoxide radical was proven to be the main active radical to decompose the tetracycline molecules. Therein, the tetracycline molecules were degraded to water and carbon dioxide by dihydroxylation-demethylation-ring opening reactions. This work investigates the effect of crystal planes on heterojunction types through two different exposed crystal planes of bismuth vanadate oxide, which can provide some basic research and theoretical support for the progressive and controlled synthesis of photocatalysts with heterojunction structures.
两种类型 II 和 Z 方案都可以很好地解释异质结结构的电荷转移行为,但氧化铋钒和氮化碳之间形成的异质结结构类型仍未得到明确。在此,我们合理地制备了具有 {010} 和 {012} 面为主的氧化铋钒和氮化碳作为装饰,构建了一个以氧化铋钒为包裹层的核壳结构,以确保相同的光催化反应界面。通过能带建立和自由基物种的研究,{010} 和 {012} 面为主的氧化铋钒/氮化碳复合材料都表现出类型 II 异质结结构,而不是 Z 型异质结。此外,为了研究类型 II 异质结的影响,进行了光催化四环素降解实验,发现 {010} 面为主的氧化铋钒/氮化碳复合材料的降解效率高于 {012} 面为主的氧化铋钒/氮化碳复合材料,这是由于其导带能更高。此外,通过自由基捕获实验和降解产物的中间检测,证明超氧自由基是主要的活性自由基,可分解四环素分子。在此,通过二羟化-脱甲基-开环反应,四环素分子被降解为水和二氧化碳。这项工作通过氧化铋钒的两种不同暴露晶面研究了晶面对异质结类型的影响,可为具有异质结结构的光催化剂的逐步和可控合成提供一些基础研究和理论支持。