class='kwd-title'>Keywords: TiO2 nanotubes, Meta'/> Enhanced photocatalytic electrochemical and photoelectrochemical properties of TiO2 nanotubes arrays modified with Cu AgCu and Bi nanoparticles obtained via radiolytic reduction
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Enhanced photocatalytic electrochemical and photoelectrochemical properties of TiO2 nanotubes arrays modified with Cu AgCu and Bi nanoparticles obtained via radiolytic reduction

机译:铜银铜和铋纳米粒子通过辐射还原还原改性后的TiO2纳米管阵列的光催化电化学和光电化学性能增强

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摘要

class="kwd-title">Keywords: TiO2 nanotubes, Metal nanoparticles, Radiolysis, Phenol degradation, Photoelectrochemical performance class="head no_bottom_margin" id="abs0015title">AbstractTiO2 nanotubes arrays (NTs), obtained via electrochemical anodization of Ti foil, were modified with monometallic (Cu, Bi) and bimetallic (AgCu) nanoparticles. Different amounts of metals’ precursors were deposited on the surface of NTs by the spin-coating technique, and the reduction of metals was performed via gamma radiolysis. Surface modification of titania was studied by EDS and XPS analysis. The results show that AgCu nanoparticles exist in a Agcore-Cushell form. Photocatalytic activity was examined under UV irradiation and phenol was used as a model pollutant of water. Over 95% of phenol degradation was achieved after 60 min of irradiation for almost all examined samples, but only slight difference in degradation efficiency (about 3%) between modified and bare NTs was observed. However, the initial phenol degradation rate and TOC removal efficiency was significantly enhanced for the samples modified with 0.31 and 0.63 mol% of Bi as well as for all the samples modified with Cu and AgCu nanoparticles in comparison with bare titania nanotubes. The saturated photocurrent, under the influence of simulated solar light irradiation, for the most active Bi- and AgCu-modified samples, was over two times higher than for pristine NTs. All the examined materials were resistant towards photocorrosion processes that enables their application for long term processes induced by light.
机译:<!-fig ft0-> <!-fig @ position =“ anchor” mode =文章f4-> <!-fig mode =“ anchred” f5-> <!-fig / graphic | fig / alternatives / graphic mode =“ anchored” m1-> class =“ kwd-title”>关键字: TiO2纳米管,金属纳米颗粒,辐射分解,苯酚降解,光电化学性能 class =“ head no_bottom_margin”摘要通过钛箔的电化学阳极氧化获得的TiO2纳米管阵列(NTs)被单金属(Cu,Bi)和双金属(AgCu)纳米粒子改性。通过旋涂技术将不同数量的金属前体沉积在NTs的表面上,并通过伽马射线分解来还原金属。通过EDS和XPS分析研究了二氧化钛的表面改性。结果表明,AgCu纳米颗粒以Agcore-Cushell形式存在。在紫外线照射下检查了光催化活性,苯酚被用作水的模型污染物。几乎所有被检样品辐照60分钟后,苯酚的降解率均超过95%,但在改性和裸露的NT之间仅观察到降解效率略有差异(约3%)。然而,与裸露的二氧化钛纳米管相比,用0.31和0.63 mol%的Bi改性的样品以及所有用Cu和AgCu纳米颗粒改性的样品的初始苯酚降解率和TOC去除效率均显着提高。对于活性最高的Bi和AgCu改性样品,在模拟太阳光照射的影响下,饱和光电流比原始NTs高两倍以上。所有检查过的材料都具有抗光腐蚀的能力,可将其应用于光诱导的长期过程。

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