电场
扫描透射电子显微镜
凝聚态物理
材料科学
费米能级
离域电子
格子(音乐)
无定形固体
电子
原子单位
局域态密度
透射电子显微镜
化学物理
分子物理学
电子结构
过渡金属
电子密度
电荷密度
拉伤
费米能量
化学
电位
异质结
电荷(物理)
作者
Jin Zhao,Zanlin Qiu,Yu Meng,Y W Li,А.В. Труханов,Wenshuo Xu,Xiaoxu Zhao
出处
期刊:Nano Letters
[American Chemical Society]
日期:2026-06-17
卷期号:26 (25): 8181-8189
标识
DOI:10.1021/acs.nanolett.6c01302
摘要
Amorphous/crystalline interfaces that combine structural distortion with local charge redistribution remain poorly understood, mainly owing to limited access to atomically well-defined single-crystalline components and correlative probes of interfacial fields. Herein, we construct atomically resolvable single-crystalline/amorphous heterointerfaces by synthesizing a library of transition metal oxytellurides and map the projected electric field and strain by combining scanning transmission electron microscopy (STEM) with four-dimensional STEM (4D-STEM). In RuTe 1.93 O 0.97, 4D-STEM reveals a locally enhanced electrostatic field whose direction reorients at the interface. Charge density maps show electron accumulation in the amorphous region and depletion in the single-crystalline region, suggesting directional electron transfer. Nanometer-scale tensile and compressive strain localized around the heterointerface is identified. Electronic structure calculations indicate enhanced Ru 4 d delocalization near the Fermi level, facilitating electron-driven reactions. This work spatially correlates atomic structure with built-in electric fields and lattice strain at disordered–ordered interfaces, providing a general route to elucidating structure–activity relationships.
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