材料科学
氮化碳
光催化
层状结构
三聚氰胺
化学工程
X射线光电子能谱
苯乙烯氧化物
催化作用
扫描电子显微镜
苯乙烯
聚合物
无机化学
有机化学
化学
共聚物
复合材料
工程类
作者
Qian Gu,Ping Jiang,Yirui Shen,Kai Zhang,Phyu Thin Wai,Agus Haryono
标识
DOI:10.1016/j.mcat.2021.111441
摘要
Abstract A lamellar porous Mo-modified carbon nitride polymers (CN-Mo) was successfully prepared by a simple bottom-up method, which involves molecule self-assembly by hydrogen bonding between uracil and melamine. Analysis Results of X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray photoelectron spectra (XPS) show that Mo element has been doped in the skeleton of carbon nitride. The optical characterization results of the as-prepared photocatalysts show that, CN-Mo has a suitable band structure that can promote the separation of carriers and expands the absorption of light. Compared with CN, CN-Mo has better photocatalytic activity for epoxidation of olefins. When the mass value (relative to melamine) of ammonium molybdate tetrahydrate is 2 %, the photocatalytic efficiency is the best for the epoxidation of styrene. And the conversion rate of styrene reaches 38.4 % and the selectivity of styrene oxide is up to 83.2 %. In addition, it can maintain the better photocatalytic performance for the epoxidation of styrene after five reaction-regeneration cycles. This finding provides an effective development direction for photocatalytic olefins epoxidation under mild conditions.
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