掺杂剂
X射线光电子能谱
光降解
材料科学
光催化
降级(电信)
晶体结构
兴奋剂
扫描电子显微镜
化学工程
光致发光
化学
结晶学
光电子学
催化作用
有机化学
复合材料
电信
计算机科学
工程类
作者
Minh‐Vien Le,Ngoc‐Quoc‐Duy Vo,Quoc-Cuong Le,Vy Anh Tran,Thi-Que-Phuong Phan,Chao‐Wei Huang,Van‐Huy Nguyen
出处
期刊:Catalysts
[Multidisciplinary Digital Publishing Institute]
日期:2021-04-28
卷期号:11 (5): 564-564
被引量:33
标识
DOI:10.3390/catal11050564
摘要
Effective La-doped SrTiO3 (Sr1−xLaxTiO3, x = 0–0.1 mol.% La-doped) nanocubes were successfully synthesized by a hydrothermal method. The influence of different La dopant concentrations on the physicochemical properties of the host structure of SrTiO3 was fully characterized. X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD) revealed that the Sr2+ in the crystal lattice of SrTiO3 was substituted by La3+. As a result, the absorption region of the Sr1−xLaxTiO3 could be extended to visible light. Scanning electron microscopy (SEM) images confirmed that their morphologies are associated with an increased surface area and an increased La-doping concentration. The decrease in the photoluminescence (PL) intensity of the dopant samples showed more defect levels created by the dopant La+3 cations in the SrTiO3 structure. The photocatalytic activities of Sr1−xLaxTiO3 were evaluated with regard to the degradation of 2-naphthol at typical conditions under artificial solar light. Among the candidates, Sr0.95La0.05TiO3 exhibited the highest photocatalytic performance for the degradation of 2-naphthol, which reached 92% degradation efficiency, corresponding to a 0.0196 min−1 degradation rate constant, within 180 minutes of irradiation. Manipulating the structure of Sr1−xLaxTiO3 nanocubes could produce a more effective and stable degradation efficiency than their parent compound, SrTiO3. The parameters remarkably influence the Sr1−xLaxTiO3 nanocubes’ structure, and their degradation efficiencies were also studied. Undoubtedly, substantial breakthroughs of Sr1−xLaxTiO3 nanocube photocatalysts toward the treatment of organic contaminants from industrial wastewater are expected shortly.
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