带材弯曲
材料科学
悬空债券
费米能级
表面状态
光电发射光谱学
带隙
解吸
密度泛函理论
吸附
离解(化学)
氢
外延
凝聚态物理
分子物理学
X射线光电子能谱
化学物理
曲面(拓扑)
纳米技术
硅
物理化学
光电子学
计算化学
化学
图层(电子)
核磁共振
几何学
有机化学
电子
物理
量子力学
数学
作者
Dominik C. Moritz,Isaac Azahel Ruiz Alvarado,Mohammad Amin Zare Pour,Agnieszka Paszuk,Tilo Frieß,Erich Runge,Jan P. Hofmann,Thomas Hannappel,W. G. Schmidt,Wolfram Jaegermann
标识
DOI:10.1021/acsami.2c13352
摘要
Stable InP (001) surfaces are characterized by fully occupied and empty surface states close to the bulk valence and conduction band edges, respectively. The present photoemission data show, however, a surface Fermi level pinning only slightly below the midgap energy which gives rise to an appreciable surface band bending. By means of density functional theory calculations, it is shown that this apparent discrepancy is due to surface defects that form at finite temperature. In particular, the desorption of hydrogen from metalorganic vapor phase epitaxy grown P-rich InP (001) surfaces exposes partially filled P dangling bonds that give rise to band gap states. These defects are investigated with respect to surface reactivity in contact with molecular water by low-temperature water adsorption experiments using photoemission spectroscopy and are compared to our computational results. Interestingly, these hydrogen-related gap states are robust with respect to water adsorption, provided that water does not dissociate. Because significant water dissociation is expected to occur at steps rather than terraces, surface band bending of a flat InP (001) surface is not affected by water exposure.
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