High-Performance Room-Light-Driven β-AgVO3/mpg-C3N4 Core/Shell Photocatalyst Prepared by Mechanochemical Method

H. Kosslick, Yingyong Wang, M. F. Ibad, Xiangyun Guo, M. Lütgens, S. Lochbrunner, Marcus Frank, N. Q. Liem, A. Schulz
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引用次数: 2

Abstract

A new highly efficient, visible light active, silver vanadate/polymeric carbonitride “core/shell” photocatalyst was prepared mechano-chemically prepared by grinding mixtures of β-silver vanadate and mesoporous graphitic carbonitride. Besides the core/shell photocatalyst, β-silver vanadate/mesoporous polymeric carbonitride composites and supported mpg-C3N4@β-silver vanadates were prepared. The materials were characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), nitrogen ad- and de-sorption, diffuse reflectance UV-Vis measurement (DRS), infrared spectroscopy, Raman microscopy, and time-resolved photoluminescence spectroscopy. The photocatalytic performance of the materials was investigated in the degradation of organics using pharmaceutical ibuprofen and 4-(isobutyl phenyl) propionic acid sodium salt as model compounds under batch conditions. Reaction intermediates were studied by electrospray ionization and time-of-flight mass spectrometry (ESI-TOF-MS). Additionally, the degree of mineralization was determined by total organic carbon TOC measurements. The core/shell photocatalyst has shown superior photocatalytic activity compared to the other prepared composites or supported photocatalysts as well as the single mpg-C3N4. Scavenger experiments showed that valence band holes and anionic superoxide radicals are the main active species in the photocatalytic process. TOC measurement confirmed the mineralization of the organic compound, which was in line with ESI-TOF-MS experiments. Time-resolved photoluminescence measurements indicated that charges generated in carbonitride migrate via diffusive hopping and exhibit increased mobility in the case of the silver vanadate/polymeric carbonitride composite.
机械化学法制备高性能室内光驱动β-AgVO3/mpg-C3N4核/壳光催化剂
采用机械化学方法,将β-钒酸银与介孔碳氮化石墨混合研磨,制备了一种新型高效、具有可见光活性的钒酸银/聚合物碳氮化“核/壳”光催化剂。除核壳光催化剂外,还制备了β-钒酸银/介孔碳氮聚合物复合材料和负载型mpg- c3n4 @β-钒酸银。采用透射电子显微镜(TEM)、x射线衍射(XRD)、氮吸附和脱附、漫反射紫外-可见测量(DRS)、红外光谱、拉曼显微镜和时间分辨光致发光光谱对材料进行了表征。以药用布洛芬和4-(异丁基苯基)丙酸钠盐为模型化合物,在间歇条件下考察了材料的光催化降解有机物的性能。通过电喷雾电离和飞行时间质谱(ESI-TOF-MS)对反应中间体进行了研究。此外,矿化程度由总有机碳TOC测定。与其他制备的复合材料或负载型光催化剂以及单个mpg-C3N4相比,该核/壳型光催化剂表现出优异的光催化活性。清除率实验表明,价带空穴和阴离子超氧自由基是光催化过程中的主要活性物质。TOC测定证实了有机化合物的矿化,这与ESI-TOF-MS实验结果一致。时间分辨光致发光测量表明,碳氮化物中产生的电荷通过扩散跳变迁移,并且在钒酸银/聚合物碳氮化物复合材料中表现出更高的迁移率。
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