电荷密度
材料科学
扫描透射电子显微镜
空间电荷
电子
分子物理学
电子密度
显微镜
光学
物理
化学物理
透射电子显微镜
纳米技术
量子力学
作者
Wenpei Gao,Christopher Addiego,Hui Wang,Xingxu Yan,Yusheng Hou,Dianxiang Ji,Colin Heikes,Yi Zhang,Linze Li,Huaixun Huyan,Tom Blum,Toshihiro Aoki,Yuefeng Nie,Darrell G. Schlom,Ruqian Wu,Xiaoqing Pan
出处
期刊:Nature
[Springer Nature]
日期:2019-10-14
卷期号:575 (7783): 480-484
被引量:106
标识
DOI:10.1038/s41586-019-1649-6
摘要
The distribution of charge density in materials dictates their chemical bonding, electronic transport, and optical and mechanical properties. Indirectly measuring the charge density of bulk materials is possible through X-ray or electron diffraction techniques by fitting their structure factors1-3, but only if the sample is perfectly homogeneous within the area illuminated by the beam. Meanwhile, scanning tunnelling microscopy and atomic force microscopy enable us to see chemical bonds, but only on the surface4-6. It remains a challenge to resolve charge density in nanostructures and functional materials with imperfect crystalline structures-such as those with defects, interfaces or boundaries at which new physics emerges. Here we describe the development of a real-space imaging technique that can directly map the local charge density of crystalline materials with sub-angstrom resolution, using scanning transmission electron microscopy alongside an angle-resolved pixellated fast-electron detector. Using this technique, we image the interfacial charge distribution and ferroelectric polarization in a SrTiO3/BiFeO3 heterojunction in four dimensions, and discover charge accumulation at the interface that is induced by the penetration of the polarization field of BiFeO3. We validate this finding through side-by-side comparison with density functional theory calculations. Our charge-density imaging method advances electron microscopy from detecting atoms to imaging electron distributions, providing a new way of studying local bonding in crystalline solids.
科研通智能强力驱动
Strongly Powered by AbleSci AI