4.8 Article

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

期刊

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 135, 期 32, 页码 12068-12075

出版社

AMER CHEMICAL SOC
DOI: 10.1021/ja405585s

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资金

  1. Marie Curie Actions program for the award of an Intra-European Fellowship (FUNSURF) [pief-ga-2009-254009]
  2. Interuniversity Attraction Poles Programme [P7/05]
  3. Belgian Science Policy Office and the Research Fund of KU Leuven [GOA 11/003]
  4. Fund of Scientific Research - Flanders (FWO)
  5. Agency for Innovation by Science and Technology in Flanders (IWT)
  6. Ministry of Education, Culture, Sports, Science, and Technology, Japan [21245012, 23111710]
  7. Grants-in-Aid for Scientific Research [21245012, 21106001] Funding Source: KAKEN

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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.

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