Achieving Highly Efficient Photoelectrochemical Water Oxidation with a TiCl(4) Treated 3D Antimony-Doped SnO(2) Macropore/Branched α-Fe(2)O(3) Nanorod Heterojunction Photoanode

利用TiCl₄处理的三维锑掺杂SnO₂大孔/分支α-Fe₂O₃纳米棒异质结光阳极实现高效光电化学水氧化

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Abstract

Utilizing photoelectrochemical (PEC) cells to directly collecting solar energy into chemical fuels (e.g., H(2) via water splitting) is a promising way to tackle the energy challenge. α-Fe(2)O(3) has emerged as a desirable photoanode material in a PEC cell due to its wide spectrum absorption range, chemical stability, and earth abundant component. However, the short excited state lifetime, poor minority charge carrier mobility, and long light penetration depth hamper its application. Recently, the elegantly designed hierarchical macroporous composite nanomaterial has emerged as a strong candidate for photoelectrical applications. Here, a novel 3D antimony-doped SnO(2) (ATO) macroporous structure is demonstrated as a transparent conducting scaffold to load 1D hematite nanorod to form a composite material for efficient PEC water splitting. An enormous enhancement in PEC performance is found in the 3D electrode compared to the controlled planar one, due to the outstanding light harvesting and charge transport. A facile and simple TiCl(4) treatment further introduces the Ti doping into the hematite while simultaneously forming a passivation layer to eliminate adverse reactions. The results indicate that the structural design and nanoengineering are an effective strategy to boost the PEC performance in order to bring more potential devices into practical use.

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