Facile synthesis of sunlight driven photocatalysts Zn0.9Ho0.05M0.05O (M = Pr, Sm, Er) for the removal of synthetic dyes from wastewater

材料科学 光降解 掺杂剂 甲基橙 结晶度 兴奋剂 光化学 带隙 纤锌矿晶体结构 光催化 可见光谱 核化学 有机化学 催化作用 光电子学 化学 冶金 复合材料
作者
Muhammad Nadeem,Tauseef Munawar,Faisal Mukhtar,Sumaira Manzoor,K. Mahmood,M. S. Al-Buriahi,Khadijah Mohammedsaleh Katubi,Muhammad Naeem Ashiq,Imed Boukhris,Faisal Iqbal
出处
期刊:Surfaces and Interfaces [Elsevier BV]
卷期号:34: 102376-102376 被引量:5
标识
DOI:10.1016/j.surfin.2022.102376
摘要

Currently, environmental pollution due to contaminants released from industries into clean water is a big challenge to maintain public health worldwide. The elimination of organic toxins, particularly organic dyes using semiconductor-mediated photocatalysis is an efficient technique. Herein, Zn0.9Ho0.05M0.05O (M = Pr, Sm, Er) photocatalysts were prepared by the co-precipitation method and characterized via state-of-art techniques to study the structural, optical, electrochemical, and morphological properties. XRD results confirmed that the grown ZnO-based catalysts have hexagonal wurtzite structures with high crystallinity and successful co-doping. FTIR and Raman analysis have shown the vibrational bands and optical phonon modes of ZnO in all catalysts with a small shift which further evident the co-doping. Roughly spherical morphology revealed by FE-SEM images with improvement by co-doping. The energy bandgap of grown ZnO depends on dopants and is decreased by co-doping compared to single-doped samples, as evident from UV-Visible analysis. The photocatalytic degradation experiment towards methyl orange (MO) and methylene blue (MB) dyes under sunlight exhibited that co-doped catalysts have higher efficiency against both dyes. Remarkably, Ho-Er co-doped catalyst degraded 99.7% MB and 84% MO dye under 60 min sunlight illumination with a higher apparent rate constant of 0.0975 and 0.028 min−1, respectively, with stability up to 6th cycle against MB dye. The scavenger tests demonstrate that the major role in the enhanced photodegradation is superoxide (O2*−) and hydroxyl (OH*) radicals. The boosted photocatalytic activity is due to the lower energy bandgap, and the higher flow of charge carrier (EIS results) led to the higher generation of reactive species. Moreover, these consequences revealed that the individual performance of ZnO could be boosted through rare earth elements co-doping to make it useful for environmental applications.
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