Temperature-Enhanced Solvent Vapor Annealing of a C3 Symmetric Hexa-peri-Hexabenzocoronene: Controlling the Self-Assembly from Nano- to Macroscale

被引:54
作者
Treossi, Emanuele [1 ]
Liscio, Andrea [1 ]
Feng, Xinliang [2 ]
Palermo, Vincenzo [1 ]
Muellen, Klaus [2 ]
Samori, Paolo [3 ]
机构
[1] CNR, Ist Sintesi Organ & Fotoreattivita, I-40129 Bologna, Italy
[2] Max Planck Inst Polymer Res, D-55124 Mainz, Germany
[3] Univ Louis Pasteur 8, CNRS, ISIS 7006, Nanochem Lab, F-67083 Strasbourg, France
关键词
annealing; nanocrystals; scanning probe microscopy; self-assembly; thin layers; SINGLE POLYMER-CHAINS; THIN-FILM; FORCE MICROSCOPY; CHARGE-TRANSPORT; MOLECULAR WIRES; X-RAY; SURFACE; TRANSISTORS; MOBILITY; SEMICONDUCTOR;
D O I
10.1002/smll.200801002
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Temperature-enhanced solvent vapor annealing (TESVA) is used to self assemble functionalized polycyclic aromatic hydrocarbon molecules into ordered macroscopic layers and crystals on solid surfaces. A novel C-3 symmetric hexa-peri-hexabenzocoronene functionalized with alternating hydrophilic and hydrophobic side chains is used as a model system since its multivalent character can be expected to offer unique self-assembly properties and behavior in different solvents. TESVA promotes the molecule's long-range mobility, as proven by their diffusion on a Si/SiOx surface on a scale of hundreds of micrometers. This leads to self-assembly into large, ordered crystals featuring an edge-on columnar type of arrangement, which differs from the morphologies obtained using conventional solution-processing methods such as spin-coating or drop-casting. The temperature modulation in the TESVA makes it possible to achieve an additional control over the role of hydrodynamic forces in the self-assembly at surfaces, leading to a macroscopic self-healing within the adsorbed film notably improved as compared to conventional solvent vapor annealing. This surface re-organization can be monitored in real time by optical and atomic force microscopy.
引用
收藏
页码:112 / 119
页数:8
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