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In situ green oxidation synthesis of Ti(3+) and N self-doped SrTiO(x)N(y) nanoparticles with enhanced photocatalytic activity under visible light

A simple in situ green oxidation synthesis route was developed to prepare Ti(3+) and N self-doped SrTiO(x)N(y) nanoparticles using TiN and H(2)O(2) as precursors. X-ray diffraction (XRD), scanning electron microscopy (SEM) and high-resolution transmission electron microscopy (HRTEM) were used to cha...

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Detalles Bibliográficos
Autores principales: Liu, Jiandong, Ma, Xiaohong, Yang, Lina, Liu, Xingliang, Han, Aixia, Lv, Haitang, Zhang, Chao, Xu, Shiai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9078412/
https://www.ncbi.nlm.nih.gov/pubmed/35540354
http://dx.doi.org/10.1039/c7ra13523h
Descripción
Sumario:A simple in situ green oxidation synthesis route was developed to prepare Ti(3+) and N self-doped SrTiO(x)N(y) nanoparticles using TiN and H(2)O(2) as precursors. X-ray diffraction (XRD), scanning electron microscopy (SEM) and high-resolution transmission electron microscopy (HRTEM) were used to characterize the crystallinity, structure and morphology. X-ray photoelectron spectroscopy (XPS) tests confirmed the presence of Ti(3+) and N in the prepared SrTiO(x)N(y) nanoparticles. The resultant nanoparticles were shown to have strong absorption from 400 to 800 nm using UV-vis diffuse reflectance spectroscopy (UV-vis DRS). The formation mechanism of the Ti(3+) and N self-doped SrTiO(x)N(y) nanoparticles was also discussed. Under visible light irradiation, the obtained Ti(3+) and N self-doped samples showed higher photocatalytic activity for the degradation of the model wastewater, methylene blue (MB) solution. The most active sample T-130-Vac, obtained at 130 °C under vacuum, showed a 9.5-fold enhancement in the visible light decomposition of MB in comparison to the commercial catalyst nano-SrTiO(3). The sample also showed a relatively high cycling stability for photocatalytic activity.