Temperature-Induced Structural Phase Transitions in a Two-Dimensional Self-Assembled Network

被引:174
作者
Blunt, Matthew O. [1 ]
Adisoejoso, Jinne [1 ]
Tahara, Kazukuni [2 ]
Katayama, Keisuke [2 ]
Van der Auweraer, Mark [1 ]
Tobe, Yoshito [2 ]
De Feyter, Steven [1 ]
机构
[1] KU Leuven Univ Leuven, Dept Chem, Div Mol Imaging & Photon, Lab Photochem & Spect, B-3001 Louvain, Belgium
[2] Osaka Univ, Grad Sch Engn Sci, Div Frontier Mat Sci, Toyonaka, Osaka 5608531, Japan
关键词
LIQUID-SOLID INTERFACE; RESTRICT CONFORMATIONAL FREEDOM; ESTABLISH QUALITATIVE TRENDS; POROUS MOLECULAR NETWORKS; ONE BUILDING-BLOCK; SUPRAMOLECULAR NETWORKS; QUANTITATIVE MODEL; TORSIONAL ENTROPY; ACID MONOLAYERS; HEPTANOIC ACID;
D O I
10.1021/ja405585s
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Two-dimensional (2D) supramolecular self-assembly at liquid-solid interfaces is a thermodynamically complex process producing a variety of structures. The formation of multiple network morphologies from the same molecular building blocks is a common occurrence. We use scanning tunnelling microscopy (STM) to investigate a structural phase transition between a densely packed and a porous phase of an alkylated dehydrobenzo[12]annulene (DBA) derivative physisorbed at a solvent-graphite interface. The influence of temperature and concentration are studied and the results combined using a thermodynamic model to measure enthalpy and entropy changes associated with the transition. These experimental results are compared to corresponding values obtained from simulations and theoretical calculations. This comparison highlights the importance of considering the solvent when modeling porous self-assembled networks. The results also demonstrate the power of using structural phase transitions to study the thermodynamics of these systems and will have implications for the development of predictive models for 2D self-assembly.
引用
收藏
页码:12068 / 12075
页数:8
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