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Facile synthesis of new, highly efficient SnO2/carbon nitride composite photocatalysts for the hydrogen evolution reaction

机译:易于合成用于氢析出反应的新型高效SnO2 /氮化碳复合光催化剂

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摘要

Novel SnO2/carbon nitride photocatalysts having surface areas up to 220 m(2) g(-1) were prepared for the first time by condensation of dicyandiamide in alkali metal chloride/SnCl2-containing salt melts at 550 degrees C, without the use of hard templates. XRD and HR-TEM investigations showed that the obtained materials are composed of 5-10 nm SnO2 nanoparticles deposited onto nanosheets set up from 1D-melon ribbons. The morphology and crystalline structure of products appear to be greatly dependent on the synthesis temperature. SnO2/carbon nitride composites are found to be highly efficient in the photocatalytic reactions, as exemplified by Rhodamine B degradation and water reduction using Pt as a cocatalyst. Under the optimized synthesis conditions, these composite photocatalysts achieve hydrogen evolution rates more than 2 times higher than the mesoporous carbon nitride (mp-CN) under visible light irradiation. In principle, this new method based on utilization of MCl/SnCl2 salt melts as a reaction medium allows carrying out various polymerization reactions in the presence of the mild Lewis acid in the solution phase in the wide temperature range of 180-550 degrees C. Moreover, SnCl2 eutectics are even suitable for post-synthesis modification of the bulk carbon nitride to tune its morphology and greatly increase the surface area and photocatalytic activity.
机译:通过在550摄氏度下在不使用碱金属氯化物/含SnCl2的盐熔体中缩合双氰胺,首次制备了表面积高达220 m(2)g(-1)的新型SnO2 /碳氮化物光催化剂。硬模板。 XRD和HR-TEM研究表明,所获得的材料由5-10 nm SnO2纳米颗粒组成,这些纳米颗粒沉积在由1D西瓜带制成的纳米片上。产物的形态和晶体结构似乎在很大程度上取决于合成温度。发现SnO2 /碳氮化物复合物在光催化反应中非常高效,例如罗丹明B降解和使用Pt作为助催化剂的水还原就是例证。在最优化的合成条件下,这些复合光催化剂在可见光照射下的氢释放速率是中孔氮化碳(mp-CN)的2倍以上。原则上,这种基于利用MCl / SnCl2盐熔体作为反应介质的新方法可以在温和的路易斯酸存在下于180-550℃的宽温度范围内在溶液相中进行各种聚合反应。 SnCl2共晶体甚至适用于本体氮化碳的合成后改性,以调整其形态并大大增加表面积和光催化活性。

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