苝四羧酸二酰亚胺修饰增强g-C_(3)N_(4)光催化性能EI北大核心CSCD

以3,4,9,10-苝四甲酸二酐和L-天冬氨酸为原料,合成水溶性苝二酰亚胺衍生物N,N′-二(2-丁二酸基)-3,4,9,10-苝四羧酸二酰亚胺(PASP)。采用水热法将PASP接枝在g-C_(3)N_(4)上,制备PASP改性g-C_(3)N_(4)复合光催化剂(g-C_(3)N_(4)-PASP)。通过X射线衍射仪(XRD)、傅里叶变换红外光谱仪(FT-IR)、X射线光电子能谱仪(XPS)、扫描电子显微镜(SEM)、透射电子显微镜(TEM)、紫外-可见光漫反射光谱(UV-Vis DRS)和固体荧光光谱等对g-C_(3)N_(4)-PASP的组成、结构、形貌和光学性质等进行表征,考察g-C_(3)N_(4)-PASP对水溶液中模型污染物亚甲基蓝(MB)的光催化降解活性。结果表明:g-C_(3)N_(4)与PASP经水热反应,可通过酰胺键共价结合;相比纯g-C_(3)N_(4),g-C_(3)N_(4)-PASP比表面积显著增大,吸收带边红移至614 nm,同时PASP修饰可促进g-C_(3)N_(4)材料表面光生电子和空穴分离,进而有效提升光催化活性。在可见光(λ>420 nm)照射下,g-C_(3)N_(4)-PASP对MB的降解率60 min内可达99.4%,降解速率常数k约为g-C_(3)N_(4)的2倍。

Perylene tetracarboxylic bisimide decorated g-C3 N4 with enhanced photocatalytic activity

A water-soluble perylene bisimide derivative, N, N'-di(2-succinic acid)-perylene-3, 4, 9, 10-tetracarboxylic bisimide (PASP) was synthesized by using 3, 4, 9, 10-perylenetetracarboxylic dianhydride and L-aspartic acid as starting materials. The PASP were grafted onto graphitic carbon nitride (g-C₃N₄) via hydrothermal method to prepare PASP modified g-C₃N₄ hybrid photocatalyst (g-C₃N₄-PASP). The composition, structure, morphology and optical properties of the prepared g-C₃N₄-PASP samples were typically characterized by X-ray diffraction(XRD), Fourier transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy(XPS), scanning electron microscopy(SEM), transmission electron microscopy(TEM), UV-Vis diffuse reflectance spectroscopy(UV-Vis DRS), and solid-state fluorescence spectroscopy. In addition, the photocatalytic activities of the prepared g-C₃N₄-PASP photocatalysts were evaluated by decomposition of methylene blue(MB) pollutant in water solution under visible light. The results reveal that PASP can be facilely linked to the g-C₃N₄ covalently via amide bond by hydrothermal treatment; compared to pristine g-C₃N₄, the g-C₃N₄-PASP possesses obviously higher specific surface area, dramatic red shifted absorption edge of 614 nm, and more efficient charge separation. Therefore, the visible light photo-catalytic degradation of MB pollution in water over the g-C₃N₄-PASP is notably improved. The g-C₃N₄-PASP could degrade 99.4% of MB dyes in 60 min under visible light irradiations (λ >420 nm), with a pseudo-first-order rate constant 2 times higher than that of pristine g-C₃N₄.