Stability of functionalized platform molecules on Au(111)

被引:15
|
作者
Jasper-Toennies, Torben [1 ]
Poltavsky, Igor [2 ]
Ulrich, Sandra [3 ]
Moje, Tobias [3 ]
Tkatchenko, Alexandre [2 ]
Herges, Rainer [3 ]
Berndt, Richard [1 ]
机构
[1] Christian Albrechts Univ Kiel, Inst Expt & Angew Phys, D-24098 Kiel, Germany
[2] Univ Luxembourg, Phys & Mat Sci Res Unit, L-1511 Luxembourg, Luxembourg
[3] Christian Albrechts Univ Kiel, Otto Diels Inst Organ Chem, D-24098 Kiel, Germany
来源
JOURNAL OF CHEMICAL PHYSICS | 2018年 / 149卷 / 24期
关键词
RANGE OSCILLATORY INTERACTION; SINGLE MOLECULES; TRIPODAL ANCHOR; GOLD; SURFACE; CATALYSIS; SELECTIVITY; TRANSPORT; NOBLE;
D O I
10.1063/1.5059344
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Trioxatriangulenium (TOTA) platform molecules were functionalized with methyl, ethyl, ethynyl, propynyl, and hydrogen and sublimated onto Au(111) surfaces. Low-temperature scanning tunneling microscopy data reveal that >99% of ethyl-TOTA and methyl-TOTA remain intact, whereas 60% of H-TOTA and >99% of propynyl-TOTA and ethynyl-TOTA decompose. The observed tendency toward fragmentation on Au(111) is opposite to the sequence of gas-phase stabilities of the molecules. Although Au(111) is the noblest of all metal surfaces, the binding energies of the decomposition products to Au(111) destabilize the functionalized platforms by 2 to 3.9 eV (190-370 kJ/mol) and even render some of them unstable as revealed by density functional theory calculations. Van der Waals forces are important, as they drive the adsorption of the platform molecules. Published by AIP Publishing.
引用
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页数:8
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