Piot Luc, Marchenko Alexandr, Wu Jishan, Müllen Klaus, Fichou Denis
CEA-Saclay, LRC Nanostructures et Semiconducteurs Organiques (CNRS-CEA-UPMC), SPCSI/DRECAM, 91191-Gif-sur-Yvette, France.
J Am Chem Soc. 2005 Nov 23;127(46):16245-50. doi: 10.1021/ja0548844.
The growth and structure of self-assembled adlayers of hexakis(n-dodecyl)-peri-hexabenzocoronene (HBC-C12) adsorbed on highly ordered pyrolitic graphite (HOPG) decorated by an n-pentacontane (n-C50H102) monolayer have been investigated by scanning tunneling microscopy (STM). Whereas on HOPG the HBC-C12 molecules readily self-assemble into a unique stable 2D structure, on the [n-C50H102 monolayer/graphite] system we observe morphological phase transitions with formation of time dependent alpha, beta, and gamma phases (alpha-->beta-->gamma). The initial alpha-phase is similar to that obtained on bare graphite, while intermediate beta- and final gamma-structures present molecular dimers and rows, respectively. The observed two-dimensional polymorphism is due to weak interaction between HBC-C12 molecules and n-C50H102-modified graphite substrate. Our results constitute an important step toward the control of the growth and structure of highly ordered monolayers of functional conjugated molecules by modifying the graphite surface with an n-alkane monolayer of appropriate chain length.
通过扫描隧道显微镜(STM)研究了吸附在由正五十烷(n-C50H102)单层修饰的高度有序热解石墨(HOPG)上的六(正十二烷基)-周-六苯并蔻(HBC-C12)自组装吸附层的生长和结构。在HOPG上,HBC-C12分子很容易自组装成独特的稳定二维结构,而在[n-C50H102单层/石墨]体系中,我们观察到形态相变,形成了随时间变化的α、β和γ相(α→β→γ)。初始的α相类似于在裸石墨上获得的相,而中间的β相和最终的γ结构分别呈现分子二聚体和分子行。观察到的二维多态性是由于HBC-C12分子与n-C50H102修饰的石墨基底之间的弱相互作用。我们的结果是通过用适当链长的正构烷烃单层修饰石墨表面,朝着控制功能共轭分子高度有序单层的生长和结构迈出的重要一步。