单层
吸附
物理
化学物理
金属
散射
电子
电子转移
半导体
电荷(物理)
原子物理学
电子散射
共振(粒子物理)
苝
分子物理学
结晶学
物理化学
材料科学
纳米技术
荧光
化学
光学
光电子学
量子力学
冶金
作者
Manuel Marks,N. Armbrust,J. Güdde,U. Höfer
标识
DOI:10.1088/1367-2630/abb0c3
摘要
Abstract We study the role of electronic interface states on the electron transfer dynamics between layers of the organic semiconductor 3,4,9,10-perylene-tetracarboxylic acid dianhydride (PTCDA) and the (111) and (100) surfaces of silver. For this purpose, we investigate the change of the decay dynamics of the first ( n = 1) image-potential state on these surfaces upon adsorption of an ordered monolayer of PTCDA by means of time-resolved two-photon photoemission (2PPE). We find that the already short lifetime of the ( n = 1)-state on Ag(111) is only slightly further reduced by PTCDA adsorption, whereas a much stronger reduction by a factor of three is observed for adsorption on Ag(100) resulting in similar lifetimes for both orientations. We show by model calculations on the basis of an analytical one-dimensional pseudo-potential that the enhanced decay for PTCDA/Ag(100) can be attributed to the opening of an additional channel for electron-electron scattering by the formation of an interface state which is derived from the Shockley-type surface resonance of Ag(100).
科研通智能强力驱动
Strongly Powered by AbleSci AI