异质结
材料科学
X射线光电子能谱
催化作用
兴奋剂
钙钛矿(结构)
费米能级
析氧
电催化剂
密度泛函理论
半导体
光电子学
化学工程
化学
物理化学
电极
电子
计算化学
结晶学
电化学
物理
量子力学
生物化学
工程类
作者
Rajendra Paudel,Andricus R. Burton,Marcelo A. Kuroda,Byron H. Farnum,R. Comès
出处
期刊:Journal of vacuum science & technology
[American Vacuum Society]
日期:2023-10-03
卷期号:41 (6)
被引量:4
摘要
Iron and nickel-based perovskite oxides have proven promising for the oxygen evolution reaction (OER) in alkaline environments, as their catalytic overpotentials rival precious metal catalysts when the band alignment is tuned through substitutional doping or alloying. Here, we report the engineering of band alignment in LaFeO3/LaNiO3 (LFO/LNO) heterostructures via interfacial doping that yields greatly enhanced catalytic performance. The 0.2 eV offset (VBO) between the Fermi level in metallic LNO and the valence band in semiconducting LFO that we predict using density functional theory makes LFO a p-type semiconductor, resulting in significantly lower barriers for hole transport through LFO compared to the intrinsic material. Experimental band alignment measured with in situ x-ray photoelectron spectroscopy of epitaxial LFO/LNO heterostructures confirms these predictions, producing a measured VBO of 0.3(1) eV. Furthermore, OER catalytic measurements on these samples in the alkaline solution show an increase in catalytic current density by a factor of ∼275 compared to LFO grown on n-type Nb-doped SrTiO3. These results demonstrate the power of tuning band alignments through interfacial band engineering for improved catalytic performance of oxides.
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