All that Glitters Is Not Gold: A Probe into Photocatalytic Nitrate Reduction Mechanism over Noble Metal Doped and Undoped TiO2
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Date
2017
Journal Title
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American Chemical Society service@acs.org
Abstract
Photocatalytic reduction of aqueous nitrate has been thoroughly studied over noble metals doped and pristine TiO<inf>2</inf> synthesized by a customized single step microwave assisted hydrothermal method. The synthesized catalysts are systematically characterized using XRD, Raman spectroscopy, FE-SEM, HR-TEM, XPS, diffuse reflectance spectroscopy, and PL measurements. The characterization reveals the successful synthesis of highly crystalline doped and undoped nano-TiO<inf>2</inf>. The photocatalytic rate of aqueous nitrate reduction over undoped TiO<inf>2</inf> is found to be higher than that of noble metal doped TiO<inf>2</inf>. Mechanistic studies of the photocatalytic reduction are carried out with the help of different hole (oxalic acid, and methanol) and electron (sodium persulfate) scavengers, which reveal that the photogenerated electrons are the primary agents toward efficient nitrate photoreduction. Detailed studies have revealed that the noble metal doping in TiO<inf>2</inf> helps in efficient photogeneration of H<inf>2</inf> compared to the undoped analogue, however, the in situ produced H<inf>2</inf> is found to be inefficient in reducing NO<inf>3</inf>-. The conduction band position from first principle calculations with respect to the nitrate and hydrogen reduction potentials derived from cyclic voltammetry provide insights to the electron transfer process in determining the reaction pathway. © 2017 American Chemical Society.
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Keywords
Cyclic voltammetry, Electron transport properties, Metals, Nitrates, Oxalic acid, Precious metals, Single crystals, Titanium dioxide, Diffuse reflectance spectroscopy, Electron transfer process, First principle calculations, Mechanistic studies, Microwave-assisted hydrothermal, Nitrate photoreduction, Photocatalytic reduction, Photogenerated electrons, Titanium compounds
Citation
Journal of Physical Chemistry C, 2017, 121, 49, pp. 27406-27416
