轨道能级差
极化子
有机半导体
电子迁移率
并五苯
半导体
材料科学
凝聚态物理
密度泛函理论
化学物理
电子能带结构
分子内力
化学
电子
物理
计算化学
光电子学
纳米技术
分子
量子力学
薄膜晶体管
立体化学
有机化学
图层(电子)
作者
Haruki Sato,Syed A. Abd. Rahman,Yota Yamada,Hiroyuki Ishii,Hiroyuki Yoshida
出处
期刊:Nature Materials
[Nature Portfolio]
日期:2022-07-18
卷期号:21 (8): 910-916
被引量:31
标识
DOI:10.1038/s41563-022-01308-z
摘要
The energy band structure provides crucial information on charge transport behaviour in organic semiconductors, such as effective mass, transfer integrals and electron-phonon coupling. Despite the discovery of the valence (the highest occupied molecular orbital (HOMO)) band structure in the 1990s, the conduction band (the lowest unoccupied molecular orbital (LUMO)) has not been experimentally observed. Here we employ angle-resolved low-energy inverse photoelectron spectroscopy to reveal the LUMO band structure of pentacene, a prototypical high-mobility organic semiconductor. The derived transfer integrals and bandwidths from the LUMO are substantially smaller than those predicted by density functional theory calculations. To reproduce this bandwidth reduction, we propose an improved (partially dressed) polaron model that accounts for the electron-intramolecular vibrational interaction with frequency-dependent coupling constants based on Debye relaxation. This model quantitatively reproduces not only the transfer integrals, but also the temperature-dependent HOMO and LUMO bandwidths, and the hole and electron mobilities. The present results demonstrate that electron mobility in high-mobility organic semiconductors is indeed limited by polaron formation.
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