硫脲
三聚氰胺
氮化碳
石墨氮化碳
尿素
产量(工程)
热解
核化学
化学
微观结构
量子产额
光催化
热稳定性
氮化物
碳纤维
材料科学
有机化学
催化作用
结晶学
复合数
荧光
复合材料
量子力学
物理
图层(电子)
冶金
作者
Wendong Zhang,Qin Zhang,Fan Dong,Zaiwang Zhao
摘要
Polymeric graphitic carbon nitride (g-C3N4) materials were prepared by direct pyrolysis of thiourea, dicyandiamide, melamine, and urea under the same conditions, respectively. In order to investigate the effects of precursors on the intrinsic physicochemical properties of g-C3N4, a variety of characterization tools were employed to analyze the samples. The photocatalytic activity of the samples was evaluated by the removal of NO in gas phase under visible light irradiation. The results showed that the as-prepared CN-T (from thiourea), CN-D (from dicyandiamide), CN-M (from melamine), and CN-U (from urea) exhibited significantly different morphologies and microstructures. The band gaps of CN-T, CN-D, CN-M, and CN-U were 2.51, 2.58, 2.56, and 2.88 eV, respectively. Both thermal stability and yield are in the following order: CN-M > CN-D > CN-T > CN-U. The photoactivity of CN-U (31.9%) is higher than that of CN-T (29.6%), CN-D (22.2%), and CN-M (26.8%). Considering the cost, toxicity, and yield of the precursors and the properties of g-C3N4, the best precursor for preparation of g-C3N4was melamine. The present work could provide new insights into the selection of suitable precursor for g-C3N4synthesis and in-depth understanding of the microstructure-dependent photocatalytic activity of g-C3N4.
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