Controllable preparation of YPrO3 photocatalystvia sol-gel method with enhanced photocatalytic performance under ultraviolet light

IF 3.2 3区 化学 Q2 CHEMISTRY, INORGANIC & NUCLEAR
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Abstract

In this work, an ultraviolet light-driven YPrO3 photocatalyst was successfully synthesized via the sol-gel method, utilizing yttrium nitrate hexahydrate (Y(NO3)3·6H2O) and praseodymium nitrate hexahydrate (Pr(NO3)3·6H2O) as the yttrium and praseodymium sources, respectively, with oxalic acid dihydrate (H2C2O4·2H2O) serving as an auxiliary solvent. In addition, the prepared samples were characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy(XPS), thermogravimetric and differential scanning calorimetry (TG-DSC), ultraviolet visible diffuse reflectance spectroscopy (UV VisDRS), and an electrochemical workstation. Also, the photocatalytic activity of YPrO3 samples was explored by using methyl orange (MO) solutionas a model pollutant to simulate wastewater under varying synthesis temperatures and illumination durations. The material with the highest degradation efficiency was subjected to cycling and recovery experiments to assess its stability. Furthermore, the photocatalytic mechanism of YPrO3 was investigated. Experimental results revealed that pure YPrO3 samples could be effectively synthesized at calcination temperatures ranging from 850 °C to 1000 °C, with the sample prepared at 900 °C exhibiting the optimal photocatalytic activity. This sample possessed an average grain size of 4–5 μm. Under UV light irradiation for 90min, the YPrO3 sampleprepared at 900°Cachieved approximately 80 % degradation of methyl orange at an initial concentration of 5 mg/L. After five consecutive cycles, the degradation rate remained as high as 70.39 %, with no change in the crystal structure, indicating excellent stability. The photocatalytic mechanism of YPrO3 was found to involve the synergetic effect of superoxide radicals and photogenerated holes in degrading pollutants. In conclusion, YPrO3could be a promising photocatalyst with excellent performance, holding broad application prospects.

Abstract Image

利用溶胶-凝胶法制备可控的 YPrO3 光催化剂,提高其在紫外线下的光催化性能
本研究以六水合硝酸钇(Y(NO3)3-6H2O)和六水合硝酸镨(Pr(NO3)3-6H2O)分别作为钇源和镨源,以二水合草酸(H2C2O4-2H2O)作为辅助溶剂,通过溶胶-凝胶法成功合成了紫外光驱动的YPrO3光催化剂。此外,还使用 X 射线衍射 (XRD)、扫描电子显微镜 (SEM)、傅立叶变换红外光谱 (FT-IR)、X 射线光电子能谱 (XPS)、热重和差示扫描量热 (TG-DSC)、紫外可见光漫反射光谱 (UV VisDRS) 和电化学工作站对制备的样品进行了表征。此外,还以甲基橙(MO)溶液为模型污染物,模拟废水在不同合成温度和光照时间下的情况,探讨了 YPrO3 样品的光催化活性。对降解效率最高的材料进行了循环和回收实验,以评估其稳定性。此外,还研究了 YPrO3 的光催化机理。实验结果表明,纯 YPrO3 样品可在 850 ℃ 至 1000 ℃ 的煅烧温度下有效合成,其中 900 ℃ 制备的样品具有最佳光催化活性。该样品的平均粒度为 4-5 μm。在紫外光照射 90 分钟后,900 ℃ 下制备的 YPrO3 样品对初始浓度为 5 mg/L 的甲基橙的降解率约为 80%。连续五个循环后,降解率仍高达 70.39%,晶体结构未发生变化,表明其稳定性极佳。研究发现,YPrO3 的光催化机理涉及超氧自由基和光生空穴降解污染物的协同效应。总之,YPrO3 是一种性能优异的光催化剂,具有广阔的应用前景。
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来源期刊
Journal of Solid State Chemistry
Journal of Solid State Chemistry 化学-无机化学与核化学
CiteScore
6.00
自引率
9.10%
发文量
848
审稿时长
25 days
期刊介绍: Covering major developments in the field of solid state chemistry and related areas such as ceramics and amorphous materials, the Journal of Solid State Chemistry features studies of chemical, structural, thermodynamic, electronic, magnetic, and optical properties and processes in solids.
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