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Morphology Control and Photocatalysis Enhancement by the One-Pot Synthesis of Carbon Nitride from Preorganized Hydrogen-Bonded Supramolecular Precursors

机译:预先结合氢键的超分子前体一锅法合成氮化碳的形态控制和光催化作用的增强

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摘要

We present an efficient synthesis of a modified carbon nitride photocatalyst by using supramolecular complexes of cyanuric acid, melamine, and 2,4-diamino-6-phenyl-1,3,5-triazine as precursors. We combined a self-templating approach for morphology control with the modification of photophysical properties by altering the chemical structure of the material. The resulting carbon nitrides exhibit high surface areas, defined morphologies, and a strong enhancement of light absorption in the visible-light region. A detailed analysis shows that the ratio changes of the three raw monomers resulted in different carbon nitride morphologies, absorption, and emission properties, along with the incorporation of different numbers of phenyl groups in the resulting carbon nitride structures. The modified carbon nitrides exhibit superior activity in the photodegradation of rhodamine B, up to 16 times that of bulk carbon nitride. The pyrolysis of rationally chosen supramolecular hydrogen-bonded precursors constitutes a synthetic pathway for the simple one-pot preparation of efficient, metal-free carbon nitride photocatalysts.
机译:我们目前通过使用氰尿酸,三聚氰胺和2,4-二氨基-6-苯基-1,3,5-三嗪的超分子络合物作为前体,高效合成改性的氮化碳光催化剂。我们通过改变材料的化学结构,将自模板方法用于形态控制与光物理性质的修改相结合。所得的碳氮化物表现出高的表面积,确定的形态以及在可见光区域的光吸收的强烈增强。详细的分析表明,三种原料单体的比例变化导致不同的氮化碳形态,吸收和发射特性,以及在所得的氮化碳结构中引入不同数量的苯基。改性的氮化碳在若丹明B的光降解中表现出优异的活性,最高可达本体氮化碳的16倍。合理选择的超分子氢键合前体的热解构成了简单的一锅法制备高效,无金属的氮化碳光催化剂的合成途径。

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