光催化
三聚氰酸
材料科学
三聚氰胺
氮化碳
化学工程
催化作用
石墨氮化碳
熔盐
结晶
三聚氯氰
氮化物
纳米技术
有机化学
复合材料
化学
高分子化学
冶金
工程类
图层(电子)
作者
Yang Li,Dainan Zhang,Jiajie Fan,Quanjun Xiang
出处
期刊:Chinese Journal of Catalysis
[China Science Publishing & Media Ltd.]
日期:2020-08-28
卷期号:42 (4): 627-636
被引量:147
标识
DOI:10.1016/s1872-2067(20)63684-1
摘要
Graphitic carbon nitride (g-C3N4) has emerged as a remarkably promising photocatalyst for addressing environmental and energy issues; however, it exhibits only moderate photocatalytic activity because of its low specific surface area and high recombination of carriers. Preparation of crystalline g-C3N4 by the molten salt method has proven to be an effective method to improve the photocatalytic activity. However, crystalline g-C3N4 prepared by the conventional molten salt method exhibits a less regular morphology. Herein, highly crystalline g-C3N4 hollow spheres (CCNHS) were successfully prepared by the molten salt method using cyanuric acid-melamine as a precursor. The higher crystallization of the CCNHS samples not only repaired the structural defects at the surface of the CCNHS samples but also established a built-in electric field between heptazine-based g-C3N4 and triazine-based g-C3N4. The hollow structure improved the level of light energy utilization and increased the number of active sites for photocatalytic reactions. Because of the above characteristics, the as-prepared CCNHS samples simultaneously realized photocatalytic hydrogen evolution with the degradation of the plasticizer bisphenol A. This research offers a new perspective on the structural optimization of supramolecular self-assembly.
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