Synthesis of Conjugated Polymers and Small Molecules for Organic Light-Emitting Devices and Photodetectors
Doctoral thesis, 2018
In organic light-emitting devices, the emissive molecule is commonly mixed with a charge transporting host matrix, which can be either a small molecule or a conjugated polymer. The latter is beneficial since it does not require deposition of the emitter and matrix components in high vacuum and high temperature conditions. The polymeric materials can be dissolved and printed on a substrate of any desired size and production scale, at room temperature, and even under ambient air. The specific wavelength range of near-infrared (NIR) at λ >700 nm is of interest for a wide range of applications spanning from optical communication to biosensing. However, the low energy of NIR range poses challenges for the materials design, in terms of emission efficiency and light intensity, which are further addressed in this thesis, allowing the fabrication of high-performance NIR-OLEDs and NIR-LECs.
For photodetectors, absorption of a wide spectrum of light is beneficial in biosensing and imaging applications. Low noise and fast charge extraction are necessary for the detection of light at high speeds even at low intensities. These aspects are studied in this thesis by designing new polymers with different absorption, charge transport, and morphological properties in the photoactive layer. Two polymers enabled the fabrication of visible (red) OPDs with a low dark current (the main constituent in the noise), high detectivity, and high photoresponse speed.
solution processing
conjugated polymers
fluorescence
near-infrared
light-emitting electrochemical cell
organic photodetector
organic light-emitting diode
Author
Petri Henrik Murto
Chalmers, Chemistry and Chemical Engineering, Applied Chemistry
High-Performance Organic Photodetectors from a High-Bandgap Indacenodithiophene-Based π-Conjugated Donor-Acceptor Polymer
ACS Applied Materials & Interfaces,;Vol. 10(2018)p. 12937-12946
Journal article
Efficient Near-Infrared Electroluminescence at 840 nm with “Metal-Free” Small-Molecule:Polymer Blends
Advanced Materials,;Vol. 30(2018)
Journal article
High performance all-polymer photodetector comprising a donor-Acceptor-Acceptor structured indacenodithiophene-bithieno[3,4-c] pyrroletetrone copolymer
ACS Macro Letters,;Vol. 7(2018)p. 395-400
Journal article
Incorporation of Designed Donor−Acceptor−Donor Segments in a Host Polymer for Strong Near-Infrared Emission from a Large-Area Light-Emitting Electrochemical Cell
ACS Applied Energy Materials,;Vol. 1(2018)p. 1753-1761
Journal article
Intense and Stable Near-Infrared Emission from Light-Emitting Electrochemical Cells Comprising a Metal-Free Indacenodithieno[3,2-b]thiophene-Based Copolymer as the Single Emitter
Chemistry of Materials,;Vol. 29(2017)p. 7750-7759
Journal article
Triazolobenzothiadiazole-Based Copolymers for Polymer Light-Emitting Diodes: Pure Near-Infrared Emission via Optimized Energy and Charge Transfer
Advanced Optical Materials,;Vol. 4(2016)p. 2068-2076
Journal article
In this thesis, polymer-based semiconductors are designed for the attainment of emission in the special spectral range of near-infrared (NIR) region. NIR-emitting materials are used for the fabrication of high-performance light-emitting devices, which are of interest for a wide range of applications from optical communication to medical purposes. This thesis also covers the application of conjugated polymers as light-harvesting semiconductors for photodetectors. These devices convert incident light into electrical current. Photodetectors that have low noise and fast signal response allow the operation at high speeds even in low light, for example in biosensing and imaging applications.
Subject Categories
Polymer Chemistry
Materials Chemistry
Other Physics Topics
Other Chemistry Topics
Organic Chemistry
ISBN
978-91-7597-800-0
Doktorsavhandlingar vid Chalmers tekniska högskola. Ny serie: 4481
Publisher
Chalmers
Vasa A-salen, Vasa Hus 2-3 entréhall, Vera Sandbergs Allé 8, Göteborg
Opponent: Prof. Andrew P. Monkman, Durham University, UK