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首页> 外文期刊>Chemosphere >Enhanced photocatalytic reduction reaction over Bi3+-TiO2 nanoparticles in presence of formic acid as a hole scavenger
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Enhanced photocatalytic reduction reaction over Bi3+-TiO2 nanoparticles in presence of formic acid as a hole scavenger

机译:在甲酸作为空穴清除剂的情况下增强Bi3 + -TiO2纳米粒子的光催化还原反应

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A series of Bi3+-doped TiO2 (Bi3+-TiO2) catalysts with a doping concentration up to 2 wt% were prepared by a sol-gel method. The prepared photocatalysts were characterized by different means to determine their chemical composition, surface structure and light absorption properties. The photocatalytic activity of different Bi3+-TiO2 catalysts was evaluated in the photocatalytic reduction of nitrate in aqueous solution under UV illumination. In the experiments, formic acid was used as a hole scavenger to enhance the photocatalytic reduction reaction. The experiments demonstrated that nitrate was effectively degraded in aqueous Bi3+-TiO2 suspension by more than 83% within 150 min, while the pH of the solution increased from 3.19 to 5.83 due to the consumption of formic acid. The experimental results indicate that the presence of Bi3+ in TiO2 catalysts substantially enhances the photocatalytic reaction of nitrate reduction. It was found that the optimal dosage of 1.5 wt% Bi3+ in TiO2 achieved the fastest reaction of nitrate reduction under the experimental condition. Bismuth ions deposit on the TiO2 surface behaves as sites where electrons accumulate. Better separation of electrons and holes on the modified TiO2 surface allows more efficient channeling of the charge carriers into useful reduction and oxidation reactions rather than recombination reactions. Two intermediate products of nitrite and ammonia during the reaction were also monitored to explore the possible mechanisms of photoluminescence quenching and photocatalytic reduction in the context of donor-acceptor interaction with electron trapping centers. (c) 2006 Elsevier Ltd. All rights reserved.
机译:通过溶胶-凝胶法制备了一系列掺杂浓度最高为2 wt%的Bi3 +掺杂的TiO2(Bi3 + -TiO2)催化剂。用不同的方法对制备的光催化剂进行表征,以确定其化学组成,表面结构和光吸收性能。在紫外光照射下,在水溶液中硝酸盐的光催化还原中,评价了不同的Bi3 + -TiO2催化剂的光催化活性。在实验中,甲酸用作空穴清除剂以增强光催化还原反应。实验表明,硝酸盐在Bi3 + -TiO2水性悬浮液中在150分钟内有效降解了83%以上,而由于甲酸的消耗,溶液的pH从3.19增加到5.83。实验结果表明,TiO2催化剂中Bi3 +的存在大大增强了硝酸盐还原的光催化反应。发现在实验条件下,TiO2中1.5 wt%Bi3 +的最佳用量实现了最快的硝酸盐还原反应。沉积在TiO2表面的铋离子表现为电子积累的位置。改性TiO2表面上电子和空穴的更好分离允许电荷载流子更有效地引导进入有用的还原和氧化反应,而不是重组反应。还监测了反应过程中亚硝酸盐和氨的两种中间产物,以探索在供体-受体与电子俘获中心相互作用的情况下光致发光猝灭和光催化还原的可能机理。 (c)2006 Elsevier Ltd.保留所有权利。

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