Inorganic Nanoarchitectures by Organic Self-Assembly

This book explores the implementation of soft matter design principles for inorganic thin film nanoarchitectures. It presents novel and unique methods of employing soft matter self-assembly for photonic and optoelectronic.

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 TiO2 and SiO2. Novel fabrication and characterization methods allow unprecedented control of material formation on the 10 500 nm length scale, allowing the design of material architectures with interesting photonic and optoelectronic properties.

Nominated by the University of Cambridge as an outstanding Ph.D. thesis Novel and unique methods of employing soft matter self-assembly for photonic and optoelectronic devices Extended tutorials on soft matter self-assembly and on optical aspects of thin films and interfaces Includes supplementary material: sn.pub/extras

Inhalt
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.