研究目的
Investigating the surface orientation and dimensions of nanostructures of functionalized zinc phthalocyanines prepared with colloidal lithography using scanning probe microscopy.
研究成果
Nanostructures prepared using colloidal lithography provide a practical approach to control the growth and aggregation of molecules within defined areas of organosilane matrix films. The choice of pendant groups of phthalocyanines directs the orientation and surface assembly of the molecules. Both OTMS and PEO-silane proved effective as resists for site-selective binding of ZnPcs on APTES nanopatterns.
研究不足
The ex situ approach for studying molecular conformations does not monitor the same precise area of a sample during successive steps of nanopatterning, requiring average values for cursor measurements rather than real-time views or kinetic information for individual nanostructures.
1:Experimental Design and Method Selection:
Colloidal lithography combined with steps of solution immersion and vapor deposition of organosilanes was used to prepare patterned arrays of nanoholes and nanorings.
2:Sample Selection and Data Sources:
Polished silicon wafers, Si(111), were used as substrates. Size-sorted monodisperse silica and latex mesospheres with diameters of 250 and 300 nm were used as surface masks.
3:List of Experimental Equipment and Materials:
Atomic force microscopy (AFM) was used for characterization. Materials included (3-aminopropyl)triethoxysilane (APTES), octadecyltrimethoxysilane (OTMS), and 2-[methoxy(polyethyleneoxy)propyl]trichlorosilane (PEO-silane).
4:Experimental Procedures and Operational Workflow:
A surface mask of colloidal latex or silica spheres was used to protect discrete areas of a Si(111) substrate from the deposition of organosilanes. After mask removal, the uncovered areas were used for further reaction steps.
5:Data Analysis Methods:
AFM was used to analyze the size and morphology of nanostructures.
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