亚单层Be沉积诱导的GaAs(001)表面重建

IF 1.8 4区 化学 Q3 CHEMISTRY, PHYSICAL Surface Science Pub Date : 1997-04-10 Epub Date: 1998-05-19 DOI:10.1016/S0039-6028(97)01310-1
H. Oigawa, M. Wassermeier, J. Behrend, L. Däweritz, K.H. Ploog
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引用次数: 0

摘要

作为p型掺杂剂,Be诱导了GaAs(001)表面重构的变化。通过反射高能电子衍射(RHEED)和扫描隧道显微镜(STM)研究了Be覆盖0.5单层(ML)的函数。在标准分子束外延条件下,随着Be覆盖率的增加,从开始的(2 × 4)通过(2 × 3)到(1 × 2)对称,RHEED模式不断变化。这种转变的特征是1/2阶点的强度(首先在[110],然后在[110]方位角)和1/4阶点的间距(在[1¯10]方位角)都在逐渐减少。STM图像显示,表面由As和Ga/Be两种末端结构域组成。前者由(2 × 4)单元重构为(2 × 3)单元,后者由(2 × 3)单元重构为(1 × 2)单元。电子计数论证表明,畴的类型和大小是由过量电子密度与掺入的p型Be掺杂的受体密度相平衡的要求决定的。
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Reconstruction of the GaAs(001) surface induced by submonolayer Be deposition
As a p-type dopant, Be induces changes in the reconstruction of the GaAs(001) surface. This has been studied as a function of Be coverage up to 0.5 monolayer (ML) by reflection high-energy electron diffraction (RHEED) and scanning tunneling microscopy (STM). Under standard molecular beam epitaxy conditions, the RHEED pattern continuously changes with increasing Be coverage from the starting (2 × 4) via a (2 × 3) to a (1 × 2) symmetry. This transition is characterized by a gradual decrease of both, the intensity of the 1/2-order spots (first in the [110] then in the [110] azimuth) and the spacing of the 1/4-order spots (in the [1¯10] azimuth). STM images reveal that the surface is composed of both As and Ga/Be terminated domains. The former reconstruct from (2 × 4) to (2 × 3) units, the latter from (2 × 3) to (1 × 2) units. Electron-counting arguments suggest that the domain type and size are determined by the requirement that the excess electron density is balanced by the acceptor density of the incorporated p-type Be doping.
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来源期刊
Surface Science
Surface Science 化学-物理:凝聚态物理
CiteScore
3.30
自引率
5.30%
发文量
137
审稿时长
25 days
期刊介绍: Surface Science is devoted to elucidating the fundamental aspects of chemistry and physics occurring at a wide range of surfaces and interfaces and to disseminating this knowledge fast. The journal welcomes a broad spectrum of topics, including but not limited to: • model systems (e.g. in Ultra High Vacuum) under well-controlled reactive conditions • nanoscale science and engineering, including manipulation of matter at the atomic/molecular scale and assembly phenomena • reactivity of surfaces as related to various applied areas including heterogeneous catalysis, chemistry at electrified interfaces, and semiconductors functionalization • phenomena at interfaces relevant to energy storage and conversion, and fuels production and utilization • surface reactivity for environmental protection and pollution remediation • interactions at surfaces of soft matter, including polymers and biomaterials. Both experimental and theoretical work, including modeling, is within the scope of the journal. Work published in Surface Science reaches a wide readership, from chemistry and physics to biology and materials science and engineering, providing an excellent forum for cross-fertilization of ideas and broad dissemination of scientific discoveries.
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