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The Resource Inorganic Nanoarchitectures by Organic Self-Assembly, by Stefan Guldin, (electronic resource)

Inorganic Nanoarchitectures by Organic Self-Assembly, by Stefan Guldin, (electronic resource)

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Summary
Macromolecular self-assembly - driven by weak, non-covalent, intermolecular forces - is a common principle of structure formation in natural and synthetic organic materials. The variability in material arrangement on the nanometre length scale makes this an ideal way of matching  the structure-function demands of photonic and optoelectronic devices. However, suitable soft matter systems typically lack the appropriate photoactivity, conductivity or chemically stability. This thesis explores the implementation of soft matter design principles for inorganic thin film nanoarchitectures. Sacrificial block copolymers and colloids are employed as structure-directing agents for the co-assembly of solution-based inorganic materials, such as TiO_2 and SiO_2.  Novel fabrication and characterization methods allow unprecedented control of material formation on the 10 {u2013} 500 nm length scale, allowing the design of material architectures with interesting photonic and optoelectronic properties
Language
eng
Work
Publication
Extent
XVII, 165 p. 66 illus., 50 illus. in color.
Contents
  • From the Contents: Self-Assembly of Soft Matter
  • Optical aspects of thin films and interfaces
  • Structure-function interplay in dye-sensitised solar cells
  • Experimental and analytical techniques
  • Block copolymer-induced structure control for inorganic nanomaterials
  • Crystal growth in block copolymer-derived mesoporous TiO_2
Isbn
9783319003122
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http://libproxy.rpi.edu/login?url=http://dx.doi.org/10.1007/978-3-319-00312-2
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Label
Inorganic Nanoarchitectures by Organic Self-Assembly
Title
Inorganic Nanoarchitectures by Organic Self-Assembly
Statement of responsibility
by Stefan Guldin
Creator
Contributor
Author
Subject
Language
eng
Summary
Macromolecular self-assembly - driven by weak, non-covalent, intermolecular forces - is a common principle of structure formation in natural and synthetic organic materials. The variability in material arrangement on the nanometre length scale makes this an ideal way of matching  the structure-function demands of photonic and optoelectronic devices. However, suitable soft matter systems typically lack the appropriate photoactivity, conductivity or chemically stability. This thesis explores the implementation of soft matter design principles for inorganic thin film nanoarchitectures. Sacrificial block copolymers and colloids are employed as structure-directing agents for the co-assembly of solution-based inorganic materials, such as TiO_2 and SiO_2.  Novel fabrication and characterization methods allow unprecedented control of material formation on the 10 {u2013} 500 nm length scale, allowing the design of material architectures with interesting photonic and optoelectronic properties
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non fiction
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Springer Theses, Recognizing Outstanding Ph.D. Research,
Inorganic Nanoarchitectures by Organic Self-Assembly, by Stefan Guldin, (electronic resource)
Label
Inorganic Nanoarchitectures by Organic Self-Assembly, by Stefan Guldin, (electronic resource)
Link
http://libproxy.rpi.edu/login?url=http://dx.doi.org/10.1007/978-3-319-00312-2
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online resource
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cr
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Content category
text
Content type code
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Content type MARC source
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Contents
From the Contents: Self-Assembly of Soft Matter -- Optical aspects of thin films and interfaces -- Structure-function interplay in dye-sensitised solar cells -- Experimental and analytical techniques -- Block copolymer-induced structure control for inorganic nanomaterials -- Crystal growth in block copolymer-derived mesoporous TiO_2
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Extent
XVII, 165 p. 66 illus., 50 illus. in color.
File format
multiple file formats
Form of item
electronic
Isbn
9783319003122
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uncompressed
Media category
computer
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Media type code
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online resource.
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