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Photocurrent Enhancement for Ti-Doped Fe2O3 Thin Film Photoanodes by an In Situ Solid-State Reaction Method

机译:原位固相反应法增强掺Ti Fe2O3薄膜光电阳极的光电流

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In this work, a higher concentration of Ti ions are incorporated into hydrothermally grown Ti-doped (2.2% by atomic ratio) micro-nanostructured hematite films by an in situ solid-state reaction method. The doping concentration is improved from 2.2% to 19.7% after the in situ solid-state reaction. X-ray absorption analysis indicates the substitution of Fe ions by Ti ions, without the generation of Fe~(2+) defects. Photoelectrochemical impedance spectroscopy reveals the dramatic improvement of the electrical conductivity of the hematite film after the in situ solid-state reaction. As a consequence, the photocurrent density increases 8-fold (from 0.15 mA/crn~2 to 1.2 mA/cm~2), and it further increases up to ~1.5 mA/cm~2 with the adsorption of Co ions. Our findings demonstrate that the in situ solid-state reaction is an effective method to increase the doping level of Ti ions in hematite films with the retention of the micro-nanostructure of the films and enhance the photocurrent.
机译:在这项工作中,通过原位固态反应方法将更高浓度的Ti离子掺入水热生长的掺Ti(原子比为2.2%)微纳米结构的赤铁矿薄膜中。原位固态反应后,掺杂浓度从2.2%提高到19.7%。 X射线吸收分析表明Fe离子被Ti离子取代,没有生成Fe〜(2+)缺陷。光电化学阻抗谱揭示了原位固态反应后赤铁矿膜电导率的显着提高。结果,光电流密度增加了8倍(从0.15 mA / crn〜2增加到1.2 mA / cm〜2),并且随着Co离子的吸附,光电流密度进一步增加到〜1.5 mA / cm〜2。我们的发现表明,原位固相反应是提高赤铁矿薄膜中Ti离子掺杂水平并保留薄膜微纳米结构并增强光电流的有效方法。

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