化学
氧化物
电荷(物理)
金属
接口(物质)
化学物理
费米能级
凝聚态物理
核物理学
物理化学
电子
物理
量子力学
吸附
吉布斯等温线
有机化学
作者
Jiayue Wang,Jing Yang,Jenna L. Wardini,Iradwikanari Waluyo,Adrian Hunt,Ethan J. Crumlin,Neal Fairley,William J. Bowman,Harold Y. Hwang,Bilge Yildiz
摘要
Exsolution is a promising approach for fabricating oxide-supported metal nanocatalysts through redox-driven metal precipitation. A defining feature of exsolved nanocatalysts is their anchored metal-oxide interface, which exhibits exceptional structural stability in (electro)catalysis. However, the electronic interactions at this unique interface remain unclear, despite their known impact on catalytic performance. In this study, we confirm charge transfer between the host oxide and the exsolved metal by demonstrating a two-stage Fermi level (EF) evolution on SrTi0.65Fe0.35O3−δ (STF) during metallic iron (Fe0) exsolution. Combining ambient pressure X-ray photoelectron spectroscopy with theoretical analysis, we show that EF initially rises due to electron doping from oxygen vacancy formation in STF. Subsequently, upon Fe0 precipitation, EF stabilizes and becomes insensitive to further oxygen release in STF, driven by EF equilibration and charge transfer between STF and the exsolved Fe0. These findings highlight the importance of considering electronic metal–support interactions when optimizing exsolved nanocatalysts.
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