Electronic Resource

Inorganic nanoarchitectures by organic self-assembly

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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 – 500 nm length scale, allowing the design of material architectures with interesting photonic and optoelectronic properties.

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Ketersediaan

Informasi Detail

Judul Seri

Springer Theses

No. Panggil

E1641

Penerbit

Switzerland : Springer Cham., 2013

Deskripsi Fisik

xvii, 165 hlm.

Bahasa

English

ISBN/ISSN

9783319003122

Klasifikasi

NONE

Tipe Isi

text

Tipe Media

computer

Tipe Pembawa

online resource

Edisi

-

Subjek

Nanoarsitektur Inorganik
Pengorganisasian Spontan : Nano Struktur

Info Detail Spesifik

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Pernyataan Tanggungjawab

Stefan Guldin

Versi lain/terkait

Lampiran Berkas

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