首页> 外文期刊>Journal of Materials Chemistry, A. Materials for energy and sustainability >Thermally-induced desulfurization and conversion of guanidine thiocyanate into graphitic carbon nitride catalysts for hydrogen photosynthesis
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Thermally-induced desulfurization and conversion of guanidine thiocyanate into graphitic carbon nitride catalysts for hydrogen photosynthesis

机译:热诱导脱硫,并将硫氰酸胍转化为用于光合作用的石墨氮化碳催化剂

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摘要

A cheap and easily-available organosulfur compound, guanidine thiocyanate, has been used to synthesize graphitic carbon nitride (g-C3N4) by a thermally-induced desulfurization and polymerization of the precursor. Photocatalytic activity experiments demonstrated that the g-C3N4 synthesized from guanidine thiocyanate exhibited a much higher H2 evolution rate than the reference sample prepared from dicyanamide. Further improvement in the activity was achieved by optimization of the condensation temperature. Based on X-ray photoelectron spectroscopy analysis, the samples synthesized at a high temperature of 700 °C feature a high crystallinity and a low density of surface defects, with an enhanced optical absorbance extending to the visible light region. As a result, the sample prepared at 700 °C has been found to be 7 times more reactive towards photocatalytic hydrogen evolution than the sample polymerized at the normal temperature of 550 °C. Other guanidine halides have also been applied to synthesize g-C3N4 materials, and the structure and activity of the resultant g-C3N4 were compared to the carbon nitride polymer from guanidine thiocyanate.
机译:一种廉价且容易获得的有机硫化合物,硫氰酸胍,已通过前驱物的热诱导脱硫和聚合反应用于合成石墨氮化碳(g-C3N4)。光催化活性实验表明,由硫氰酸胍合成的g-C3N4比由双氰胺制备的参比样品具有更高的H2释放速率。通过优化缩合温度,进一步提高了活性。根据X射线光电子能谱分析,在700°C的高温下合成的样品具有高结晶度和低表面缺陷密度,并且光吸收率提高到可见光区域。结果,发现在700°C下制备的样品对光催化氢释放的反应活性是在550°C常温下聚合的样品的7倍。其他胍卤化物也已用于合成g-C3N4材料,并将所得g-C3N4的结构和活性与来自硫氰酸胍的氮化碳聚合物进行了比较。

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