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The growth and photochemical activity of hematite films on perovskite substrates.

机译:钙钛矿基质上赤铁矿薄膜的生长和光化学活性。

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摘要

For photochemical hydrogen production to reach acceptable efficiencies, semiconductor photolysis systems that make use of visible light must be developed. This work presents results for the photochemical activity of iron-based materials and structures. Hematite, or α-Fe2O 3, and BiFeO3 absorb light in the visible range.;Details on the growth via pulsed laser deposition of Fe2O 3 films on perovskite SrTiO3 substrates are also reported. Orientation relationships between films and single crystal or polycrystalline substrates were determined using electron backscatter diffraction. Epitaxial (0001)-oriented films were grown on SrTiO3 (111) substrates. Films on SrTiO3 (001) substrates were polycrystalline, but showed preferred orientations based on alignment of close-packed (eutactic) networks. Films on polycrystalline SrTiO3 substrates also showed alignment of eutactic networks between substrate and film. The heteroepitaxial growth of polycrystalline films on polycrystalline substrates presents a much wider range of orientation conditions than available for growth on single crystals. Combinatorial substrate epitaxy, the growth and analysis using electron backscatter diffraction of films on polycrystalline substrates, opens many opportunities for wide-ranging epitaxy studies.;The photochemical behavior of BiFiO3 surfaces is reported. BiFeO3 surfaces exhibit spatially selective visible-light photochemical activity. Silver ions in solution were photochemically reduced by the BiFeO 3, depositing solid silver on the surface in patterns corresponding to positive ferroelectric domains. This is suggested to arise from upward band bending in the negative domains that prevents electrons from reaching the surface and these locations do not reduce silver. Electric fields arising from ferroelectric domains at the surface overwhelm anisotropy in the photochemical activity that might arise from grain orientation alone.;The photochemical reactivity of bulk Fe2O3 and thin Fe2O3 films on single crystal and polycrystalline substrates is reported. Bulk Fe2O3 crystallites show strong anisotropic photochemical activity. Crystallites with a surface orientation near the hexagonal (1210) plane are significantly more reactive than other orientations. Thin Fe2O3 films supported on SrTiO3 (111) substrates are significantly more reactive than similar films on Al2O3 substrates and bulk polycrystalline hematite. Films on polycrystalline substrates showed similar orientation dependent reactivity as for bulk Fe2O3 crystallites, with higher reactivity than the bulk material. Overall, films supported on SrTiO 3 substrates were more reactive than the bulk material and films on Al2O3 substrates.
机译:为了使光化学制氢达到可接受的效率,必须开发利用可见光的半导体光解系统。这项工作提出了铁基材料和结构的光化学活性的结果。赤铁矿或α-Fe2O3和BiFeO3吸收可见光。;还报道了通过脉冲激光在钙钛矿SrTiO3衬底上沉积Fe2O 3膜的生长细节。使用电子背散射衍射确定薄膜与单晶或多晶衬底之间的取向关系。在SrTiO3(111)基板上生长外延(0001)取向的薄膜。 SrTiO3(001)基材上的薄膜是多晶的,但基于密排(共晶)网络的排列,显示出较好的取向。多晶SrTiO3基材上的薄膜还显示出基材和薄膜之间的共析网络对齐。多晶衬底上的多晶膜的异质外延生长提供了比可用于单晶生长更大的取向条件范围。组合衬底外延,多晶衬底上薄膜的电子背散射衍射的生长和分析为广泛的外延研究提供了许多机会。报道了BiFiO3表面的光化学行为。 BiFeO3表面表现出空间选择性的可见光光化学活性。溶液中的银离子被BiFeO 3光化学还原,从而在表面以对应于正铁电畴的图案沉积固体银。建议这是由于负域中的向上带弯曲而引起的,该向上的带弯曲防止电子到达表面,并且这些位置不会还原银。表面的铁电畴产生的电场压倒了光化学活性的各向异性,这可能仅由晶粒取向引起。报道了单晶和多晶衬底上的块状Fe2O3和Fe2O3薄膜的光化学反应性。 Fe2O3块状晶体显示出很强的各向异性光化学活性。具有接近六边形(1210)平面的表面方向的微晶比其他方向的反应性明显更高。支撑在SrTiO3(111)衬底上的Fe2O3薄膜比起Al2O3衬底和块状多晶赤铁矿上的类似薄膜,其反应性明显更高。多晶基材上的薄膜显示出与块状Fe2O3晶体相似的取向依赖性反应性,且比块状材料具有更高的反应性。总体而言,支撑在SrTiO 3衬底上的薄膜比块状材料和Al2O3衬底上的薄膜具有更高的反应性。

著录项

  • 作者

    Schultz, Andrew M.;

  • 作者单位

    Carnegie Mellon University.;

  • 授予单位 Carnegie Mellon University.;
  • 学科 Chemistry Physical.;Engineering Materials Science.
  • 学位 Ph.D.
  • 年度 2012
  • 页码 171 p.
  • 总页数 171
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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