One-Step Synthesis of Porous Graphitic Carbon Nitride and the Photocatalytic Performance under Visible-Light Irradiation

Ligang Zhang, N. Zhang, De-Long Zhang, Wenzhu Ouyang, Yong-Juan Xie
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Abstract

Porous graphitic carbon nitride (pg-C3N4) was synthesized via a facile one-step dicyandiamide (DCDA) high-temperature calcination method using heat-labile ammonium bicarbonate (NH4HCO3) as the gaseous template, and different pg-C3N4 materials were obtained by mixing various mass ratios of NH4HCO3 into DCDA. The micro-structures and -morphologies of the porous materials were characterized by X-ray diffraction (XRD) and Scanning Electron Microscope (SEM) respectively, and the photocatalytic degradation of methylene blue (MB) dye was tested under visible-light irradiation. It is found that the thermal decomposition of NH4HCO3 promoted destruction of the layer-structured g-C3N4 and increment of the specific surface area, producing more porous structures on the material surfaces, which is considered to be vital for the improvement of photocatalytic performance. Compared with the photocatalyst calcined by pure DCDA, the pg-C3N4 photocatalysts obtained by mixing the two raw materials performed better on MB dye degradation. Moreover, photocatalytic efficiency of the catalysts improved significantly with increasing NH4HCO3 contents in the raw materials. The degradation rate photocatalyzed by pg-C3N4 materials can reach more than 90% within 1.5 h, 6.5 times higher than that of the control material. It comes up to 99% at 2 h, basically achieving the complete degradation and decolorization of MB dye.
一步法合成多孔氮化石墨碳及其可见光光催化性能
以热不稳定的碳酸氢铵(NH4HCO3)为气态模板,采用简单的一步法高温煅烧法制备了多孔石墨化氮碳(pg-C3N4),并将不同质量比的NH4HCO3与DCDA混合,得到了不同的pg-C3N4材料。采用x射线衍射(XRD)和扫描电镜(SEM)分别表征了多孔材料的微观结构和形貌,并在可见光照射下测试了光催化降解亚甲基蓝(MB)染料的性能。研究发现,NH4HCO3的热分解促进了层状结构g-C3N4的破坏和比表面积的增加,在材料表面产生更多的多孔结构,这被认为是光催化性能提高的关键。与纯DCDA煅烧的光催化剂相比,两种原料混合得到的pg-C3N4光催化剂对MB染料的降解效果更好。随着原料中NH4HCO3含量的增加,催化剂的光催化效率显著提高。pg-C3N4材料光催化降解率在1.5 h内可达到90%以上,是对照材料的6.5倍。2 h可达99%,基本实现了MB染料的完全降解脱色。
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