{"title":"Photoluminescence and Photocatalytic Degradation of Methylene Blue and Methyl Red using Pr3+ Doped CdS Nanoparticles","authors":"L. Lianmawii, N. M. Singh","doi":"10.1134/S1990793124010329","DOIUrl":null,"url":null,"abstract":"<p>The reflux technique was used to synthesize praseodymium-doped cadmium sulfide nanoparticles (Pr<sup>3+</sup>: CdS) with different doping concentrations 0, 5, 7, 9 and 11 at %. According to X-ray diffraction the samples were crystalline and hexagonal phase. Agglomerations of nanoparticles were observed from scanning electron microscopy image. When excited at 423 nm transitions of <sup>3</sup>P<sub>1</sub> → <sup>3</sup>H<sub>5</sub>, <sup>3</sup>P<sub>0</sub> → <sup>3</sup>H<sub>5</sub>, <sup>3</sup>P<sub>0</sub> → <sup>3</sup>H<sub>6</sub>, <sup>3</sup>P<sub>0</sub> → <sup>3</sup>F<sub>2</sub> are obtained from the photoluminescence studies. The position, sharpness, and intensity increased with increase in concentration. Commission internationale de l’eclairage diagram shows that Pr<sup>3+</sup> doped CdS had a hue almost white light, indicating that it might be used for solid-state illumination. For degrading methylene blue and methyl red, it was found that catalyst dose of 5 mg/L, pH 9 and pH 11 shows the best degradation percentage which is 89 and 94% respectively. Pr<sup>3+</sup> doping enhanced methyl red and methylene blue degradation by photocatalyst. The experimental data matched both the Langmuir–Hinshelwood (L–H) and pseudo-first-order kinetics models. At the same ideal experimental conditions, the pseudo-first-order provided a better fit than the Langmuir–Hinshelwood kinetic model. The research suggests that Pr<sup>3+</sup> doped CdS may operate effectively as a photocatalyst to detoxify harmful colors from wastewater.</p>","PeriodicalId":768,"journal":{"name":"Russian Journal of Physical Chemistry B","volume":null,"pages":null},"PeriodicalIF":1.4000,"publicationDate":"2024-04-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Russian Journal of Physical Chemistry B","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1134/S1990793124010329","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"PHYSICS, ATOMIC, MOLECULAR & CHEMICAL","Score":null,"Total":0}
引用次数: 0
Abstract
The reflux technique was used to synthesize praseodymium-doped cadmium sulfide nanoparticles (Pr3+: CdS) with different doping concentrations 0, 5, 7, 9 and 11 at %. According to X-ray diffraction the samples were crystalline and hexagonal phase. Agglomerations of nanoparticles were observed from scanning electron microscopy image. When excited at 423 nm transitions of 3P1 → 3H5, 3P0 → 3H5, 3P0 → 3H6, 3P0 → 3F2 are obtained from the photoluminescence studies. The position, sharpness, and intensity increased with increase in concentration. Commission internationale de l’eclairage diagram shows that Pr3+ doped CdS had a hue almost white light, indicating that it might be used for solid-state illumination. For degrading methylene blue and methyl red, it was found that catalyst dose of 5 mg/L, pH 9 and pH 11 shows the best degradation percentage which is 89 and 94% respectively. Pr3+ doping enhanced methyl red and methylene blue degradation by photocatalyst. The experimental data matched both the Langmuir–Hinshelwood (L–H) and pseudo-first-order kinetics models. At the same ideal experimental conditions, the pseudo-first-order provided a better fit than the Langmuir–Hinshelwood kinetic model. The research suggests that Pr3+ doped CdS may operate effectively as a photocatalyst to detoxify harmful colors from wastewater.
期刊介绍:
Russian Journal of Physical Chemistry B: Focus on Physics is a journal that publishes studies in the following areas: elementary physical and chemical processes; structure of chemical compounds, reactivity, effect of external field and environment on chemical transformations; molecular dynamics and molecular organization; dynamics and kinetics of photoand radiation-induced processes; mechanism of chemical reactions in gas and condensed phases and at interfaces; chain and thermal processes of ignition, combustion and detonation in gases, two-phase and condensed systems; shock waves; new physical methods of examining chemical reactions; and biological processes in chemical physics.