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Substrate-Electrode Interface Engineering by an Electron-Transport Layer in Hematite Photoanode

机译:赤铁矿光阳极中电子传输层的基体-电极界面工程

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The photoelectrochemical water oxidation efficiency of photo anodes is largely limited by interfacial charge-transfer processes. Herein, a metal oxide electron-transport layer (ETL) was introduced at the substrate-electrode interface. Hematite photoanodes prepared on Li+ or WO3-modified substrates deliver higher photocurrent. It is inferred that a Li-doped Fe2O3 (Li:Fe2O3) layer with lower flat band potential than the bulk is formed. Li:Fe2O3 and WO3 are proved to function as an expressway for electron extraction. Via introducing ETL, both the charge separation and injection efficiencies are improved. The lifetime of photogenerated electrons is prolonged by 3 times, and the ratio of surface charge transfer and recombination rate is enhanced by 5 times with Li:Fe2O3 and 125 times with WO3 ETL at 1.23 V versus reversible hydrogen electrode. This result indicates the expedited electron extraction from photoanode to the substrate can suppress not only the recombination at the back contact interface but also those at the surface, which results in higher water oxidation efficiency.
机译:光阳极的光电化学水氧化效率在很大程度上受到界面电荷转移过程的限制。在此,在基板-电极界面处引入了金属氧化物电子传输层(ETL)。在Li +或WO3修饰的基材上制备的赤铁矿光阳极可提供更高的光电流。可以推断出,形成的平带电势比本体低的掺锂的Fe2O3(Li:Fe2O3)层已形成。事实证明,Li:Fe2O3和WO3可以作为电子提取的高速公路。通过引入ETL,可以改善电荷分离和注入效率。与可逆氢电极相比,Li:Fe2O3的光生电子的寿命延长了3倍,而Li:Fe2O3的表面电荷转移和复合率的比率提高了5倍,WO3 ETL的提高了125倍。该结果表明,从光电阳极到基板的快速电子提取不仅可以抑制背面接触界面处的复合,而且还可以抑制表面处的复合,从而提高了水的氧化效率。

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