Coexistence of one- and two-dimensional supramolecular assemblies of terephthalic acid on Pd(111) due to self-limiting deprotonation

被引:60
作者
Canas-Ventura, M. E. [1 ]
Klappenberger, F.
Clair, S.
Pons, S.
Kern, K.
Brune, H.
Strunskus, T.
Woell, Ch.
Fasel, R.
Barth, J. V.
机构
[1] Ecole Polytech Fed Lausanne, Inst Phys Nanostruct, CH-1015 Lausanne, Switzerland
[2] Ruhr Univ Bochum, Lehrstuhl Phys Chem 1, D-44780 Bochum, Germany
[3] Swiss Fed Labs Mat Testing & Res, Empa, CH-3602 Thun, Switzerland
[4] Univ British Columbia, Dept Chem, Vancouver, BC V6T 1Z4, Canada
[5] Univ British Columbia, Dept Phys & Astron, Vancouver, BC V6T 1Z4, Canada
[6] Max Planck Inst Festkorperforsch, D-70569 Stuttgart, Germany
关键词
D O I
10.1063/1.2364478
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
The adsorption of terephthalic acid [C6H4(COOH)(2), TPA] on a Pd(111) surface has been investigated by means of scanning tunneling microscopy (STM), x-ray photoelectron spectroscopy, and near-edge x-ray absorption fine structure spectroscopy under ultrahigh vacuum conditions at room temperature. We find the coexistence of one- (1D) and two-dimensional (2D) molecular ordering. Our analysis indicates that the 1D phase consists of intact TPA chains stabilized by a dimerization of the self-complementary carboxyl groups, whereas in the 2D phase, consisting of deprotonated entities, the molecules form lateral ionic hydrogen bonds. The supramolecular growth dynamics and the resulting structures are explained by a self-limiting deprotonation process mediated by the catalytic activity of the Pd surface. Our models for the molecular ordering are supported by molecular mechanics calculations and a simulation of high resolution STM images.
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页数:8
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