{"title":"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","authors":"Rong Chen, Jianghong Wang, Yafei Yang, Lixiang Zhang, Wenting Tu, Peisong Tang","doi":"10.1016/j.jssc.2024.124981","DOIUrl":null,"url":null,"abstract":"<div><p>In this work, an ultraviolet light-driven YPrO<sub>3</sub> photocatalyst was successfully synthesized via the sol-gel method, utilizing yttrium nitrate hexahydrate (Y(NO<sub>3</sub>)<sub>3</sub>·6H<sub>2</sub>O) and praseodymium nitrate hexahydrate (Pr(NO<sub>3</sub>)<sub>3</sub>·6H<sub>2</sub>O) as the yttrium and praseodymium sources, respectively, with oxalic acid dihydrate (H<sub>2</sub>C<sub>2</sub>O<sub>4</sub>·2H<sub>2</sub>O) 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 YPrO<sub>3</sub> 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 YPrO<sub>3</sub> was investigated. Experimental results revealed that pure YPrO<sub>3</sub> 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 YPrO<sub>3</sub> 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 YPrO<sub>3</sub> was found to involve the synergetic effect of superoxide radicals and photogenerated holes in degrading pollutants. In conclusion, YPrO<sub>3</sub>could be a promising photocatalyst with excellent performance, holding broad application prospects.</p></div>","PeriodicalId":378,"journal":{"name":"Journal of Solid State Chemistry","volume":"339 ","pages":"Article 124981"},"PeriodicalIF":3.2000,"publicationDate":"2024-08-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Controllable preparation of YPrO3 photocatalystvia sol-gel method with enhanced photocatalytic performance under ultraviolet light\",\"authors\":\"Rong Chen, Jianghong Wang, Yafei Yang, Lixiang Zhang, Wenting Tu, Peisong Tang\",\"doi\":\"10.1016/j.jssc.2024.124981\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>In this work, an ultraviolet light-driven YPrO<sub>3</sub> photocatalyst was successfully synthesized via the sol-gel method, utilizing yttrium nitrate hexahydrate (Y(NO<sub>3</sub>)<sub>3</sub>·6H<sub>2</sub>O) and praseodymium nitrate hexahydrate (Pr(NO<sub>3</sub>)<sub>3</sub>·6H<sub>2</sub>O) as the yttrium and praseodymium sources, respectively, with oxalic acid dihydrate (H<sub>2</sub>C<sub>2</sub>O<sub>4</sub>·2H<sub>2</sub>O) 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 YPrO<sub>3</sub> 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 YPrO<sub>3</sub> was investigated. Experimental results revealed that pure YPrO<sub>3</sub> 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 YPrO<sub>3</sub> 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 YPrO<sub>3</sub> was found to involve the synergetic effect of superoxide radicals and photogenerated holes in degrading pollutants. In conclusion, YPrO<sub>3</sub>could be a promising photocatalyst with excellent performance, holding broad application prospects.</p></div>\",\"PeriodicalId\":378,\"journal\":{\"name\":\"Journal of Solid State Chemistry\",\"volume\":\"339 \",\"pages\":\"Article 124981\"},\"PeriodicalIF\":3.2000,\"publicationDate\":\"2024-08-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Solid State Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0022459624004353\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, INORGANIC & NUCLEAR\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Solid State Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0022459624004353","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
Controllable preparation of YPrO3 photocatalystvia sol-gel method with enhanced photocatalytic performance under ultraviolet light
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.
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.