Fabrication of Mn/O co-doped g-C3N4: Excellent charge separation and transfer for enhancing photocatalytic activity under visible light irradiation

光催化 X射线光电子能谱 兴奋剂 可见光谱 辐照 煅烧 材料科学 光化学 降级(电信) 反应速率常数 孔雀绿 比表面积 激进的 光电子学 核化学 化学工程 化学 催化作用 物理化学 动力学 吸附 有机化学 核物理学 工程类 物理 电信 计算机科学 量子力学
作者
Xiuquan Xu,Songmei Wang,Tongjie Hu,Xiaofeng Yu,Jiapeng Wang,Chao Jia
出处
期刊:Dyes and Pigments [Elsevier BV]
卷期号:175: 108107-108107 被引量:59
标识
DOI:10.1016/j.dyepig.2019.108107
摘要

Abstract Co-doping has been proven to significantly enhance the photocatalytic performance of g-C3N4. Herein, Mn and O co-doped g-C3N4 (Mn/O-CN) composites were constructed for the first time by a simple one-pot calcining route. The systematic characterization results of XRD, FT-IR, TEM-EDS, XPS and DRS revealed that the Mn and O elements were co-doped into the CN framework successfully as Mn3+/4+ and n-π* conjugate forms, respectively. The as-prepared Mn/O-CN-2 achieved the highest visible-light-driven degradation rate constant of 0.0290 and 0.0267 min−1 for degradation of Malachite green (MG) and Amido black 10B (AB 10B), which were about 5.09 and 5.45 folds higher than that of pristine CN, respectively. The improved photocatalytic degradation property of Mn/O-CN were mainly benefited from the extended visible light utilization, the enlarged specific surface area, and the accelerated separation and transfer of photo-induced charge carriers, which were all induced by the synergistic effects of Mn and O co-doped. Finally, the active species capturing experiments proved that the superoxide radicals (·O2−) and holes (h+) acted as the predominant roles in the photocatalytic degradation process.
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