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首页> 外文期刊>Journal of Photochemistry and Photobiology, A. Chemistry >Facial synthesis of sheet-like carbon nitride from preorganized hydrogen bonded supramolecular precursors and its high efficient photocatalytic oxidation of gas-phase NO
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Facial synthesis of sheet-like carbon nitride from preorganized hydrogen bonded supramolecular precursors and its high efficient photocatalytic oxidation of gas-phase NO

机译:从属化氢键合超分子前体的片状氮化物的面部合成及其高效光催化氧化的气相NO

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In this paper, a series of sheet-like carbon nitride (CN) semiconductor photocatalysts was synthesized by facial supramolecular method using cyanuric acid (C), melamine (M) and 2,4-diamino-6-methyl-1,3,5-triazine (Mm) as precursors. It is the first report where the latter monomer was used in such synthetic route. The prepared C-M-Mm CNs possess higher specific surface areas, stronger light absorption as well as lower recombination rate of photogenerated electron-hole pairs in comparison with bulk CN. They were used on the photocatalytic oxidation (PCO) of NO (similar to 400 ppm) with injected H2O2 solution (0.044 mL min(-1)) under simulated solar-light irradiation. The results indicate that the C-M-Mm CNs exhibit tremendous enhanced photocatalytic activity, wherein the C-1-M-0-Mm(1) CN possesses the highest photocatalytic activity (94.86%). The enhanced photocatalytic performance belongs to the synergic effect of large specific surface area, wide solar-light absorption edge and high separation and transfer efficiency of photogenerated electron-hole pairs. The presence of H2O2 is also essential in the improvement of the photocatalytic efficiency via production of more active species. The main product in the PCO of NO is NO3-, which was confirmed by Ion Chromatography. In addition, the mechanism of PCO is also discussed in detail. The results indicate that O-center dot(2)- plays a leading role in the process of PCO of NO. (C) 2017 Elsevier B.V. All rights reserved.
机译:本文通过使用氰尿酸(C),三聚氰胺(M)和2,4-氨基-6-甲基-1,3,5,通过面部超分子法合成了一系列片状氮化物(CN)半导体光催化剂。 - 噻嗪(mm)作为前体。这是第一个报告,其中后者单体用于这种合成路线。制备的C-M-MM CNS具有更高的比表面积,光吸收较强的光吸收以及光生电子空穴对的较低重组率,与本体CN相比。它们在模拟太阳光照射下注射H 2 O 2溶液(0.044mL min(-1))的光催化氧化(PCO)上使用的光催化氧化(PCO)。结果表明,C-MMM CNS表现出巨大的增强光催化活性,其中C-1-M-0-MM(1)CN具有最高的光催化活性(94.86%)。增强的光催化性能属于大型表面积,广泛的太阳光吸收边缘和高分分离和光生电孔对的转移效率的协同作用。 H 2 O 2的存在对于通过生产更活跃的物种的光催化效率的改善也是必要的。 PCO的主要产物NO为NO 3-,通过离子色谱法确认。此外,还详细讨论了PCO的机制。结果表明,O中心点(2) - 在PCO的过程中起着主导作用。 (c)2017 Elsevier B.v.保留所有权利。

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