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Fabrication of Bi2O2CO3/g-C3N4 heterojunctions for efficiently photocatalytic NO in air removal : in-situ self-sacrificial synthesis, characterizations and mechanistic study

机译:Bi2O2CO3 / g-C3N4异质结的制备以有效去除空气中的光催化NO:原位自牺牲合成,表征和机理研究

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摘要

Layer-structured Bi2O2CO3/g-C3N4 heterojunction photocatalysts were successfully prepared via one-pot hydrothermal method for the first time, in which graphitic carbon nitride (g-C3N4) served as the self-sacrificial reagent to supply carbonate anions simultaneously. Our results showed that the in situ fabricated Bi2O2CO3/g-C3N4 heterojunction exhibited superior visible-light-driven photocatalytic activity for NO photocatalytic oxidation, which can be ascribed to the morphology and structure modulation during the sacrificial synthesis processes. Heterojunctions formation pathways underlying temperature- and time-dependent structure evolution were discussed in detail. The sample fabricated at 160 °C for 12 h (BOC-CN-160) showed high stability and durability, and the highest NO removal rate which is up to 34.8% under visible light irradiation. Results from photocurrent tests and electrochemical impedance spectroscopy (EIS) demonstrated that the BOC-CN-160 sample presents much more effective interface charge separation efficiency, which can contribute to its remarkably improved photocatalytic performance. Reactive radicals during the photocatalysis processes were identified by electron spin resonance (ESR) study. Combined with the quantification of reaction intermediates, the photocatalytic degradation mechanism of NO over Bi2O2CO3/g-C3N4 heterojunction photocatalyst was proposed. The novel approach developed in this study may be further extended to synthesize a series of novel and highly efficient g-C3N4-based carbonate heterojunction photocatalysts for visible light-harvesting and energy conversion applications.
机译:首次通过单锅水热法成功制备了层状Bi2O2CO3 / g-C3N4异质结光催化剂,其中石墨氮化碳(g-C3N4)作为自耗试剂同时提供碳酸根阴离子。我们的结果表明,原位制备的Bi2O2CO3 / g-C3N4异质结在NO光催化氧化方面表现出优异的可见光驱动光催化活性,这可以归因于牺牲合成过程中的形态和结构调节。详细讨论了取决于温度和时间的结构演化的异质结形成途径。在160°C下制造12 h的样品(BOC-CN-160)具有很高的稳定性和耐久性,并且在可见光照射下的最高NO去除率高达34.8%。光电流测试和电化学阻抗谱(EIS)的结果表明,BOC-CN-160样品呈现出更有效的界面电荷分离效率,这可以大大改善其光催化性能。通过电子自旋共振(ESR)研究确定了光催化过程中的反应性自由基。结合反应中间体的定量,提出了NO在Bi2O2CO3 / g-C3N4异质结光催化剂上的光催化降解机理。这项研究中开发的新方法可能会进一步扩展,以合成用于可见光收集和能量转换应用的一系列新颖且高效的基于g-C3N4的碳酸酯异质结光催化剂。

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