Key Laboratory of Groundwater Resources and Environment, Ministry of Education, Jilin University, Changchun, 130021, China.
Jilin Provincial Key Laboratory of Water Resources and Water Environment, Jilin University, Changchun, 130021, China.
Environ Sci Pollut Res Int. 2024 Sep;31(43):55836-55849. doi: 10.1007/s11356-024-34840-3. Epub 2024 Sep 9.
In this paper, a modification of g-CN was carried out by combining non-metal doping with the construction of heterojunctions, and a type II heterojunction composite, S/g-CN@β-BiO, was prepared. The phase structure, morphology, elemental composition, valence band structure, and light absorption performance of the photocatalyst were analyzed using characterization techniques such as X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and UV-vis diffuse reflectance spectroscopy (UV-vis DRS). The performance of the composite photocatalyst in the photocatalytic degradation of gaseous toluene, one of the typical volatile organic compounds (VOCs), under simulated solar light was studied. The effects of preparation conditions, toluene concentration, and recycling on the photocatalytic performance of the composite photocatalyst were investigated. The results show that under the optimal preparation conditions, S/g-CN@β-BiO achieved a degradation efficiency of 74.0% for 5 ppm toluene after 5 h of light irradiation. Although the degradation efficiency decreased to 61.2% after five cycles, it maintained 83% of its initial activity, indicating good stability of the composite photocatalyst. Free radical quenching experiments demonstrated that h was the main active species in the photocatalytic degradation of toluene, followed by ·O. Based on all experimental results, the migration law of photo-generated charges was analyzed, and a possible photocatalytic mechanism was proposed. In this study, a new material was obtained for the photocatalytic removal of VOCs by improving the photocatalytic properties of g-CN.
本文通过非金属掺杂与构建异质结相结合对 g-CN 进行了改性,制备了一种 II 型异质结复合材料 S/g-CN@β-BiO。采用 X 射线衍射(XRD)、扫描电子显微镜(SEM)、X 射线光电子能谱(XPS)和紫外可见漫反射光谱(UV-vis DRS)等表征技术对催化剂的物相结构、形貌、元素组成、价带结构和光吸收性能进行了分析。研究了复合光催化剂在模拟太阳光下光催化降解气态甲苯(一种典型挥发性有机化合物(VOCs))的性能。考察了制备条件、甲苯浓度和循环使用对复合光催化剂光催化性能的影响。结果表明,在最佳制备条件下,S/g-CN@β-BiO 对 5 ppm 甲苯的光降解效率在 5 h 照射后达到 74.0%。尽管经过五次循环后降解效率下降至 61.2%,但其仍保持初始活性的 83%,表明复合光催化剂具有良好的稳定性。自由基猝灭实验表明,h+是甲苯光催化降解的主要活性物种,其次是·O。基于所有实验结果,分析了光生载流子的迁移规律,并提出了可能的光催化机理。本研究通过提高 g-CN 的光催化性能,获得了一种用于光催化去除 VOCs 的新材料。