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Micellar Nanoreactors—Preparation and Characterization of Hexagonally Ordered Arrays of Metallic Nanodots
Author(s) -
Kästle G.,
Boyen H.G.,
Weigl F.,
Lengl G.,
Herzog T.,
Ziemann P.,
Riethmüller S.,
Mayer O.,
Hartmann C.,
Spatz J.P.,
Möller M.,
Ozawa M.,
Banhart F.,
Garnier M.G.,
Oelhafen P.
Publication year - 2003
Publication title -
advanced functional materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.069
H-Index - 322
eISSN - 1616-3028
pISSN - 1616-301X
DOI - 10.1002/adfm.200304332
Subject(s) - nanodot , nanoreactor , materials science , x ray photoelectron spectroscopy , micelle , nanotechnology , metal , chemical engineering , transmission electron microscopy , polymer , nanostructure , nanoscopic scale , nanoparticle , organic chemistry , composite material , aqueous solution , chemistry , engineering , metallurgy
The preparation of hexagonally ordered metallic nanodots was studied in detail with emphasis on the chemical state of the resulting particles. To obtain these dots, in a first step micellar structures were formed from diblock copolymers in solution. The reverse micelles themselves are capable of ligating defined amounts of a metal salt within their cores, acting as nanoreactors. After transfer of the metal‐loaded reverse micelles onto a substrate, the polymer was removed by means of different plasmas (oxygen and/or hydrogen), which also allow the metal salt to be reduced to the metallic state. In this way, ordered arrays of metallic nanodots can be prepared on various substrates. By adjusting the appropriate parameters, the separation and the size of the dots can be varied and controlled. To determine their purity, chemical state, and surface cleanliness—all of which are crucial for subsequent experiments since nanoscale structures are intrinsically surface dominated—in‐situ X‐ray photoelectron spectroscopy (XPS) and ex‐situ transmission electron microscopy (TEM) were applied, also giving information on the formation of the nanodots.