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Continuous Oxygen Vacancy Gradient in TiO_2 Photoelectrodes by a Photoelectrochemical-Driven 'Self-Purification' Process

机译:基于光电化学驱动的“自净化”过程的TiO_2光电极中的连续氧空位梯度

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摘要

Oxygen vacancies have been treated as an important material engineering tool to enhance catalytic performance; for instance, oxygen vacancies suppress charge recombination at the Schottky interface, and thus, the photocurrent can be improved. In this regard, the gradient distribution of oxygen vacancies in n-type metal oxides produces the ideal band structure for minimizing e(-)/h(+) recombination by efficient hole extraction; however, its achievement remains a daunting challenge. Here, a photoelectrochemical (PEC)-driven "self-purification" process is suggested, which can effectively generate a gradient distribution of oxygen vacancies in the thickness range of approximate to 9.5 nm. As a result, a charge transport efficiency of 95 can be achieved by efficient hole migration from the photoanode to the electrolyte. This unique protocol is expected to provide an advanced metal oxide photocatalyst and photoelectrochemical electrode that exhibit superior photocatalytic performance with enhanced charge separation.
机译:氧空位已被视为提高催化性能的重要材料工程工具;例如,氧空位抑制肖特基 接口的电荷复合,因此可以改善光电流。在这方面,n型金属氧化物中氧空位的梯度分布产生了理想的能带结构,通过高效的空穴提取使e(-)/h(+)复合最小化;然而,它的成就仍然是一项艰巨的挑战。在这里,提出了一种光电化学(PEC)驱动的“自净化”过程,该过程可以有效地产生厚度范围约为9.5 nm的氧空位梯度分布。因此,通过从光阳极到电解质的高效空穴迁移,可以实现>95%的电荷传输效率。这种独特的方案有望提供一种先进的金属氧化物光催化剂和光电化学电极,它们表现出卓越的光催化性能和增强的电荷分离。

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