Ramírez Alfonso E, Montero-Muñoz Marly, López Lizbeth L, Ramos-Ibarra J E, Coaquira Jose A H, Heinrichs Benoît, Páez Carlos A
Grupo de Catalisis, Departmento de Química, Universidad del Cauca, Popayán - Cauca, Colombia.
Institute of Physics, University of Brasilia, Brasília, DF, 70910-900, Brazil.
Sci Rep. 2021 Feb 2;11(1):2804. doi: 10.1038/s41598-020-78568-9.
In this study we report, the synthesis of ZnO and its doping with Transition Metal Oxides -TMO-, such as CrO, MnO, FeO, CoO, NiO, CuO and CuO. Various characterization techniques were employed to investigate the structural properties. The X-ray diffraction (XRD) data and Rietveld refinement confirmed the presence of TMO phases and that the ZnO structure was not affected by the doping with TMO which was corroborated using transmission Electron microscopy (TEM). Surface areas were low due to blockage of adsorption sites by particle aggregation. TMO doping concentration in the range of 3.7-5.1% was important to calculate the catalytic activity. The UV-Visible spectra showed the variation in the band gap of TMO/ZnO ranging from 3.45 to 2.46 eV. The surface catalyzed decomposition of HO was used as the model reaction to examine the photocatalytic activity following the oxygen production and the systems were compared to bulk ZnO and commercial TiO-degussa (Aeroxyde-P25). The results indicate that the introduction of TMO species increase significantly the photocatalytic activity. The sunlight photocatalytic performance in ZnO-doped was greater than bulk-ZnO and in the case of MnO, CoO, CuO and CuO surpasses TiO (P25-Degussa). This report opens up a new pathway to the design of high-performance materials used in photocatalytic degradation under visible light irradiation.
在本研究中,我们报道了氧化锌(ZnO)的合成及其与过渡金属氧化物(TMO)如氧化铬(CrO)、氧化锰(MnO)、氧化亚铁(FeO)、氧化钴(CoO)、氧化镍(NiO)、氧化铜(CuO)和氧化亚铜(Cu₂O)的掺杂。采用了各种表征技术来研究其结构性质。X射线衍射(XRD)数据和Rietveld精修证实了TMO相的存在,并且ZnO结构不受TMO掺杂的影响,这一点通过透射电子显微镜(TEM)得到了证实。由于颗粒聚集导致吸附位点受阻,表面积较低。TMO掺杂浓度在3.7 - 5.1%范围内对于计算催化活性很重要。紫外可见光谱显示TMO/ZnO的带隙在3.45至2.46电子伏特之间变化。以表面催化分解过氧化氢(H₂O₂)作为模型反应来考察光催化活性,跟踪氧气生成情况,并将这些体系与块状ZnO和商用二氧化钛Degussa(Aeroxyde - P25)进行比较。结果表明,引入TMO物种显著提高了光催化活性。掺杂ZnO的太阳光光催化性能优于块状ZnO,并且在MnO、CoO、CuO和Cu₂O的情况下超过了TiO₂(Degussa P25)。本报告为设计在可见光照射下用于光催化降解的高性能材料开辟了一条新途径。