Role of Chain Length in the Adsorption Structures and Geometric Configurations of Phenylalanine Derivatives on Ge(100) Surfaces

详细信息    查看全文

• 作者：Youngchan Park ; Heeseon Lim ; Sena Yang ; Hangil Lee
• 刊名：The Journal of Physical Chemistry C
• 出版年：2012
• 出版时间：June 14, 2012
• 年：2012
• 卷：116
• 期：23
• 页码：12655-12659
• 全文大小：289K
• 年卷期：v.116,no.23(June 14, 2012)
• ISSN：1932-7455

文摘

The variation of the adsorption structures and geometric configurations among phenylalanine derivatives (2-amino-4-phenylpropanoic acid (PhenA), 2-amino-5-phenylpropanoic acid (PhenB), and 2-amino-6-phenylpropanoic acid (PhenC)) adsorbed on Ge(100) surfaces was investigated using density functional theory (DFT) calculations. The chain length of a linker bonded to the 伪-carbon of the phenylalanine derivatives influenced the preferred adsorption structure in self-assembled monolayers (SAMs). We confirmed that the 鈥淥鈥揌 dissociated-N dative bonded structure鈥?is the most favorable structure among the five possible adsorption structures. Interestingly, geometric differences in the adsorption configurations indicated that the phenyl rings of PhenA and PhenB were tilted with respect to the Ge(100) surface, with an angle 30掳 from the surface normal. In contrast, the phenyl ring of PhenC was tilted with an angle of 60掳 with respect to the surface normal. We therefore confirmed that PhenA and PhenB are available to use in SAMs considering the geometrical configurations and the adsorption energies. The theoretical results were further supported by conducting DFT calculations of the reaction pathways, leading to the favored adsorption geometries.