首页> 外文会议>Solar Hydrogen and Nanotechnology II; Proceedings of SPIE-The International Society for Optical Engineering; vol.6650 >Photoelectrochemical and photocatalytic properties of nanocn stalline TiO_2 electrodes
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Photoelectrochemical and photocatalytic properties of nanocn stalline TiO_2 electrodes

机译:纳米档TiO_2电极的光电化学和光催化性能。

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The electrochemical and photocatalytic properties of a TiO_2 film deposited on transparent electrodes were investigated. Its electrochemical behavior was typical of an n-type semiconductor electrode. Its photocatalytic activity, investigated for phenol degradation on an optical bench (area of 1 cm~2, 5 mL of solution), revealed small currents (3 μA) and poor total organic carbon (TOC) removal (5 %) when the electrode was biased at + 1.1 V in the dark for 3 h. Under polychromatic irradiation, the electrode presented 25 μA of current and 12 % of phenol degradation. A better performance was achieved for photoelectrocatalytic configuration, when the electrode was irradiated and biased with + 0.6 V. Experiments done under irradiation with a metallic vapor lamp using 9 cm~2 electrodes and 10 mL of solution revealed that heterogeneous photocatalysis configuration (HPC) resulted in 50 % of TOC removal, while 85 % was achieved by the electro-assisted process (EHPC). Both the configurations exhibited pseudo-first order kinetics for phenol degradation, but the rate constant was two times that of EHPC. The application of a potential bias to the TiO_2 porous electrode must enhance the photogenerated electron/hole separation, which minimize the charge recombination and increases its photocatalytic activity towards organic pollutant degradation.
机译:研究了透明电极上沉积的TiO_2薄膜的电化学和光催化性能。它的电化学行为是n型半导体电极的典型特征。通过在光具座(面积为1 cm〜2,5 mL溶液)中对苯酚的降解进行研究,发现其光催化活性显示出小电流(3μA)和不良的总有机碳(TOC)去除率(5%)。在黑暗中以+ 1.1 V偏置3 h。在多色辐射下,电极呈现25μA的电流和12%的苯酚降解。当用+ 0.6 V的电压对电极进行辐照和偏压时,可以获得更好的光电催化性能。在使用9 cm〜2电极和10 mL溶液的金属蒸气灯辐照下进行的实验表明,产生了多相光催化构型(HPC)在50%的TOC去除率中,有85%是通过电辅助工艺(EHPC)实现的。两种构型均表现出苯酚降解的假一级动力学,但速率常数是EHPC的两倍。在TiO_2多孔电极上施加电势偏压必须增强光生电子/空穴的分离,从而最大程度地减少电荷复合并增加其对有机污染物降解的光催化活性。

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