材料科学
纳米材料
光催化
载流子
纳米孔
纳米颗粒
纳米技术
带材弯曲
纳米结构
化学物理
X射线光电子能谱
异质结
表面状态
电子
电子迁移率
化学工程
光电子学
化学
催化作用
工程类
生物化学
物理
量子力学
几何学
数学
曲面(拓扑)
作者
Johannes Mahl,Oliver Geßner,Johannes V. Barth,P. Feulner,Stefan Neppl
标识
DOI:10.1021/acsanm.1c02730
摘要
Zinc oxide (ZnO) nanomaterials are promising components for chemical and biological sensors and photocatalytic conversion and operate as electron collectors in photovoltaic technologies. Many of these applications involve nanostructures in contact with liquids or exposed to ambient atmosphere. Under these conditions, single-crystal ZnO surfaces are known to form narrow electron accumulation layers with few nanometer spatial penetration into the bulk. A key question is to what extent such pronounced surface potential gradients can develop in the nanophases of ZnO, where they would dominate the catalytic activity by modulating charge-carrier mobility and lifetimes. Here, we follow the temperature-dependent surface electronic structure of nanoporous ZnO with photoemission spectroscopy to reveal a sizable, spatially averaged downward band bending for the hydroxylated state and a conservative upper bound of <6 nm for the spatial extent of the associated potential gradient. This nanoscale confinement of conduction-band electrons to the nanoparticle film surface is crucial for a microscopic understanding and further optimization of charge transport and photocatalytic function in complex ZnO nanomaterials.
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