首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >All that Glitters Is Not Gold: A Probe into Photocatalytic Nitrate Reduction Mechanism over Noble Metal Doped and Undoped TiO2
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All that Glitters Is Not Gold: A Probe into Photocatalytic Nitrate Reduction Mechanism over Noble Metal Doped and Undoped TiO2

机译:所有闪闪发光的都不是金色:贵金属掺杂和未掺杂TiO2的光催化硝酸盐还原机制的探头

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Photocatalytic reduction of aqueous nitrate has been thoroughly studied over noble metals doped and pristine TiO2 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-TiO2. The photocatalytic rate of aqueous nitrate reduction over undoped TiO2 is found to be higher than that of noble metal doped TiO2. 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 TiO2 helps in efficient photogeneration of H-2 compared to the undoped analogue, however, the in situ produced H-2 is found to be inefficient in reducing NO3-. 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.
机译:通过定制的单步微波辅助水热法,通过定制的单步微波辅助水热法彻底研究了硝酸盐水溶液的含水水溶液和丙氨酸TiO2。使用XRD,拉曼光谱,Fe-SEM,HR-TEM,XPS,漫反射光谱和PL测量来系统地表征合成催化剂。表征揭示了高度结晶掺杂和未掺杂的纳米TiO2的成功合成。发现未掺杂的TiO 2上的硝酸盐水溶液的光催化速率高于惰性金属掺杂TiO2。光催化还原的机械研究是在不同孔(草酸和甲醇)和电子(过硫酸钠)清除剂的帮助下进行的,这表明光敏电子是朝向有效硝酸盐光电的主要试剂。详细研究表明,与未掺杂的类似物相比,TiO 2中的贵金属掺杂有助于H-2的有效光源,然而,发现原位产生的H-2在还原NO 3中是低效的。来自第一原理计算的导通带位置相对于氮酸盐和氢还原电位源自循环伏安法,为确定反应途径的电子转移过程提供了洞察力。

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