Synthesis of Self-Assembled Metal-Oxide Nanostructures in a Diblock Copolymer Matrix and Integration onto Semiconductor Surfaces

2000 ◽  
Vol 642 ◽  
Author(s):  
Robert F. Mulligan ◽  
Agis A. Iliadis ◽  
U. Lee ◽  
Peter Kofinas
Keyword(s):  
Block Copolymer ◽  
Diblock Copolymer ◽  
Photoelectron Spectroscopy ◽  
Ring Opening ◽  
Diblock Copolymers ◽  
X Ray ◽  
Oxide Nanostructures ◽  
Metal Oxide Nanostructures ◽  
Self Assembled ◽  
Zno Nanoclusters

ABSTRACTThe synthesis of self-assembled ZnO nanostructures at room temperature using a microphase separated diblock copolymer as a template is reported. Poly(norbornene) / poly(norbornene-dicarboxylic acid) diblock copolymers were synthesized using Ring Opening Metathesis Polymerization (ROMP). The polymers were dissolved and the solutions were doped with ZnCl2. Films were formed from this solution, and subsequently reacted with NH4OH. This converted the ZnCl2 into ZnO contained within the microphase-separated nanodomains of the block copolymer. Fourier Transform Infrared Spectroscopy verified the association of the metal to the second block of the polymer, and X-ray Photoelectron Spectroscopy verified the conversion of the salt to ZnO nanoclusters. The development of such ZnO - block copolymer nanocomposites is targeting the functionalization of nanostructures into device technologies.

Interaction of nitric oxide with Ru(II) complexes of deuteroporphyrindimethylester derivatives

2009 ◽  
Vol 13 (01) ◽  
pp. 35-40 ◽  
Author(s):  
Rudy Martin ◽  
Roberto Cao ◽  
Ana M. Esteva ◽  
Franz-Peter Montforts
Keyword(s):  
Nitric Oxide ◽  
Photoelectron Spectroscopy ◽  
Gold Electrode ◽  
Charge Transfer Band ◽  
Bathochromic Shift ◽  
Considerable Change ◽  
Cathodic Peak ◽  
X Ray ◽  
Polycrystalline Gold ◽  
Self Assembled

A new ruthenium(II) porphyrin disulphide derivative, [ Ru ( Pds )( CO )], was obtained from ruthenium(II)(carbonyl)deuteroporphyrin(IX), [ Ru ( DPdc )( CO )] and cystamine. The interaction of this complex with nitric oxide was studied spectrophotometrically and a bathochromic shift of the charge transfer band and considerable change in the α and β bands of the complex were observed. According to the IR spectrum, the product of this interaction is [ Ru ( DmDP )( NO +)( NO 2-)]. [ Ru ( Pds )( CO )] was then self-assembled on polycrystalline gold and characterized by X-ray photoelectron spectroscopy. [ Ru ( Pds )( CO )] was also self-assembled on gold electrode beads and its interaction with nitric oxide in aqueous solution was studied by cyclic voltammetry. A shift in the ruthenium redox process and a new irreversible cathodic peak at -0.59 V were observed, both indicating coordination of NO .

scholarly journals X-ray spectroscopy characterization of self-assembled monolayers of nitrile-substituted oligo(phenylene ethynylene)s with variable chain length

2012 ◽  
Vol 3 ◽  
pp. 12-24 ◽  
Author(s):  
Hicham Hamoudi ◽  
Ping Kao ◽  
Alexei Nefedov ◽  
David L Allara ◽  
Michael Zharnikov
Keyword(s):  
Chain Length ◽  
Photoelectron Spectroscopy ◽  
Self Assembled Monolayers ◽  
Phenylene Ethynylene ◽  
X Ray ◽  
Molecular Length ◽  
Assembled Monolayers ◽  
Self Assembled ◽  
Gold Thiolate

Self-assembled monolayers (SAMs) of nitrile-substituted oligo(phenylene ethynylene) thiols (NC-OPEn) with a variable chain length n (n ranging from one to three structural units) on Au(111) were studied by synchrotron-based high-resolution X-ray photoelectron spectroscopy and near-edge absorption fine-structure spectroscopy. The experimental data suggest that the NC-OPEn molecules form well-defined SAMs on Au(111), with all the molecules bound to the substrate through the gold–thiolate anchor and the nitrile tail groups located at the SAM–ambient interface. The packing density in these SAMs was found to be close to that of alkanethiolate monolayers on Au(111), independent of the chain length. Similar behavior was found for the molecular inclination, with an average tilt angle of ~33–36° for all the target systems. In contrast, the average twist of the OPEn backbone (planar conformation) was found to depend on the molecular length, being close to 45° for the films comprising the short OPE chains and ~53.5° for the long chains. Analysis of the data suggests that the attachment of the nitrile moiety, which served as a spectroscopic marker group, to the OPEn backbone did not significantly affect the molecular orientation in the SAMs.

Improved Functional Capabilities of Quasi-Two-Dimensional Tungsten Oxide Nanostructures

2016 ◽  
Vol 689 ◽  
pp. 55-59
Author(s):  
Serge Zhuiykov
Keyword(s):  
Photoelectron Spectroscopy ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
Current Sensing ◽  
X Ray ◽  
Force Microscopy ◽  
Functional Capabilities ◽  
Atomic Force ◽  
Oxide Nanostructures ◽  
Afm Analysis

Electrical properties and morphology of orthorhombic β–WO3 nano-flakes with thickness of ~7-9 nm were investigated at the nanoscale using energy dispersive X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and current sensing force spectroscopy atomic force microscopy (CSFS-AFM, or PeakForce TUNATM). CSFS-AFM analysis established good correlation between the topography of the developed nanostructures and various features of WO3 nano-flakes synthesized via a two-step sol-gel-exfoliation method. It was determined that β–WO3 nano-flakes annealed at 550°C possess distinguished and exceptional thickness-dependent properties in comparison with the bulk, micro- and nano-structured WO3 synthesized at alternative temperatures.

Infiltration Synthesis of Diverse Metal Oxide Nanostructures from Epoxidized Diene–Styrene Block Copolymer Templates

2019 ◽  
Vol 1 (4) ◽  
pp. 672-683 ◽  
Author(s):  
Daniel H. Yi ◽  
Chang-Yong Nam ◽  
Gregory Doerk ◽  
Charles T. Black ◽  
Robert B. Grubbs
Keyword(s):  
Block Copolymer ◽  
Metal Oxide ◽  
Oxide Nanostructures ◽  
Metal Oxide Nanostructures
Sign in / Sign up

Export Citation Format

Share Document