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Synthesis and Characterization of Enhanced Photocatalytic Activity with Li(+)-Doping Nanosized TiO(2) Catalyst

[Image: see text] The photocatalytic efficiency of TiO(2) is reduced by rapid electron–hole recombination. An effective approach to address this limitation is to have TiO(2) doped with various metal ions or heteroatoms. Herein, we prepared a series of Li(+)-doped TiO(2) nanoparticles showing high ph...

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Detalles Bibliográficos
Autores principales: Zou, Fengxia, Hu, Jianwei, Miao, Wujian, Shen, Yongjun, Ding, Jiandong, Jing, Xiaohui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7658938/
https://www.ncbi.nlm.nih.gov/pubmed/33195901
http://dx.doi.org/10.1021/acsomega.0c03054
Descripción
Sumario:[Image: see text] The photocatalytic efficiency of TiO(2) is reduced by rapid electron–hole recombination. An effective approach to address this limitation is to have TiO(2) doped with various metal ions or heteroatoms. Herein, we prepared a series of Li(+)-doped TiO(2) nanoparticles showing high photocatalytic activities through the sol–gel method. The samples were characterized by X-ray diffraction (XRD) and surface area analyses. Effects of Li(+) doping on the Brunauer–Emmett–Teller (BET) surface area, crystallite size, phase transformation temperature, and phase composition were studied. The results showed that Li(+) doping can promote the generation of the rutile crystal phase in TiO(2), lower the anatase-to-rutile transformation temperature, and generate the mixed-crystal effect. The photocatalytic degradation of methyl orange (MO) was used as a probe reaction to evaluate the photoactivity of the nanoparticles. Parameters affecting the photocatalytic efficiency, including the Li(+) doping amount, calcination temperature, and catalyst amount, as well as the kinetics of the photocatalytic process toward the degradation of MO, were investigated. The mixed-crystal TiO(2), which was doped with 1.0 mol % Li(+) and calcined at 550 °C containing 27.1% rutile and 72.9% anatase phase, showed a 2.2-fold increase in the photoactivity on the basis of the rate constant of MO decomposition as compared with the undoped TiO(2). The existence of a definite quantity of rutile phase could effectively inhibit the recombination of the electron–hole pairs, thus promoting photocatalytic activity.