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分析 BiVO/金属氧化物异质结构的界面特性及其对结性质的影响。

Analysis of the interfacial characteristics of BiVO/metal oxide heterostructures and its implication on their junction properties.

机构信息

Surface Science Division, Department of Materials Science, Technical University Darmstadt, D-64287 Darmstadt, Germany.

出版信息

Phys Chem Chem Phys. 2019 Feb 27;21(9):5086-5096. doi: 10.1039/c8cp07483f.

Abstract

The formation of heterostructures has proven to be a viable way to achieve high photoelectrochemical water splitting efficiencies with BiVO4 based photoanodes. Especially, cobalt and nickel based oxides are suitable low cost contact materials. However, the exact role of these contact materials is not yet completely understood because of the difficulty to individually quantify the effects of surface passivation, charge carrier separation and catalysis on the efficiency of a heterostructure. In this study, we used photoelectron spectroscopy in combination with in situ thin film deposition to obtain direct information on the interface structure between polycrystalline BiVO4 and NiO, CoOx and Sn-doped In2O3 (ITO). Strong upwards band bending was observed for the BiVO4/NiO and BiVO4/CoOx interfaces without observing chemical changes in BiVO4, while limited band bending and reduction of Bi and V was observed while forming the BiVO4/ITO interface. Thus, the tunability of the Fermi level position within BiVO4 seems to be limited to a certain range. The feasibility of high upwards band bending through junctions with high work function (WF) compounds demonstrate that nickel oxide and cobalt oxide are able to enhance the charge carrier separation in BiVO4. Similar studies could help to identify whether new photoelectrode materials and their heterostructures would be suitable for photoelectrochemical water splitting.

摘要

异质结构的形成已被证明是一种可行的方法,可以实现基于 BiVO4 的光阳极的高光光电化学水分解效率。特别是钴和镍基氧化物是合适的低成本接触材料。然而,由于难以单独量化表面钝化、载流子分离和催化对异质结效率的影响,这些接触材料的确切作用尚不完全清楚。在这项研究中,我们使用光电子能谱结合原位薄膜沉积,获得了多晶 BiVO4 与 NiO、CoOx 和 Sn 掺杂 In2O3(ITO)之间界面结构的直接信息。观察到 BiVO4/NiO 和 BiVO4/CoOx 界面的能带向上强烈弯曲,而没有观察到 BiVO4 中的化学变化,而在形成 BiVO4/ITO 界面时,仅观察到能带弯曲和 Bi 和 V 的减少。因此,BiVO4 中费米能级位置的可调谐性似乎限于一定范围。通过与高功函数(WF)化合物形成的结实现高向上能带弯曲的可行性表明,氧化镍和氧化钴能够增强 BiVO4 中的载流子分离。类似的研究可以帮助确定新的光电电极材料及其异质结构是否适合光电化学水分解。

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