原子单位
带偏移量
材料科学
极地的
不对称
电子
半导体
离子
氧化物
化学物理
纳米技术
偏移量(计算机科学)
光谱学
GSM演进的增强数据速率
接口(物质)
光电子学
化学
物理
计算机科学
带隙
复合材料
毛细管数
天文
毛细管作用
程序设计语言
量子力学
冶金
有机化学
价带
电信
作者
Naoyuki Nakagawa,Harold Y. Hwang,David A. Muller
出处
期刊:Nature Materials
[Springer Nature]
日期:2006-01-22
卷期号:5 (3): 204-209
被引量:1502
摘要
A central goal of modern materials physics and nanoscience is the control of materials and their interfaces to atomic dimensions. For interfaces between polar and nonpolar layers, this goal is thwarted by a polar catastrophe that forces an interfacial reconstruction. In traditional semiconductors, this reconstruction is achieved by an atomic disordering and stoichiometry change at the interface, but a new option is available in multivalent oxides: if the electrons can move, the atoms do not have to. Using atomic-scale electron energy loss spectroscopy, we have examined the microscopic distribution of charge and ions across the (001) LaAlO3/SrTiO3 interface. We find that there is a fundamental asymmetry between the ionically compensated AlO2/SrO/TiO2 interface, and the electronically compensated AlO2/LaO/TiO2 interface, both in interfacial sharpness and charge density. This suggests a general strategy to design sharp interfaces, remove interfacial screening charges, control the band offset and, hence, markedly improve the performance of oxide devices.
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