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Luminescent Radicals for Next Generation Optoelectronics

Reference Number
EP/Z534249/1
Title
Luminescent Radicals for Next Generation Optoelectronics
Status
Started
Energy Categories
Energy Efficiency(Residential and commercial)
Renewable Energy Sources(Solar Energy, Photovoltaics)
Not Energy Related
Research Types
Basic and strategic applied research
Science and Technology Fields
PHYSICAL SCIENCES AND MATHEMATICS (Chemistry)
PHYSICAL SCIENCES AND MATHEMATICS (Physics)
UKERC Cross Cutting Characterisation
Not Cross-cutting
Principal Investigator
Dr H Bronstein
Chemistry
University College London
Award Type
Standard
Funding Source
EPSRC
Start Date
01 April 2025
End Date
31 March 2028
Duration
36 months
Total Grant Value
£1,618,043
Industrial Sectors
Unknown
Region
London
Programme
NC : Physical Sciences
Investigators
Principal Investigator
Dr H Bronstein, Chemistry, University College London
Other Investigator
Dr E Evans, Swansea University
Dr A Rao, Physics, University of Cambridge
Dr H Stern, University of Oxford
Web Site
Objectives
Abstract
The development of new materials and devices that are relevant towards achieving net-zero either by energy generation OR by reducing power consumption is of critical importance to avoid the worst effects of climate change. Closed shell organic semiconductors have been phenomenally successful in energy related device applications. Organic Light Emitting Diodes (OLEDs) have become ubiquitous technology and organic photovoltaic devices (OPV) have efficiencies approaching those of conventional inorganic technologies. In order to move beyond the state-of-the-art it is necessary to overcome the fundamental issue associated with dark, low energy triplet states in these materials. We propose to create a new family of organic semiconductors and devices based on open-shell materials. The materials have the unique combination of high luminescence efficiency and absence of lower energy dark states meaning that the major loss processes in current generation optoelectronic devices can be overcome. Additionally, the presence of unpaired electrons means that these materials can also be used to optically generate high-spin states for use in quantum applications. Following on from our initial discovery that organic radicals based on (tris(2,4,6-trichlorophenyl) methyl) TTM can be made emissive through correct chemical functionalization. We propose a series of chemical systems which will achieve improved and unique optical properties. We will then use these new materials to understand and demonstrate their performance in a series of (spin)optical device applications. Specifically we will aim to design i) highly emissive, stable organic radicals with narrow FWHM for use in display technology. ii) strongly absorbing radical based polymers for use in organic photovoltaics and iii) high-spin radical systems which can be optically manipulated. Thus we propose a true paradigm shift in organic optoelectronic design and function by moving from closed-shell to open-shell systems. In doing so we believe that we open the door to a new chapter of spin and optically active materials which retain or improve upon all the benefits of traditional organic semiconductors whilst eliminating their biggest problems
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Added to Database
07/01/26