Marc K. Etherington

ORCID: 0000-0003-2101-5757
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Research Areas
  • X-ray Diffraction in Crystallography
  • Crystallization and Solubility Studies
  • Luminescence and Fluorescent Materials
  • Organic Light-Emitting Diodes Research
  • Organic Electronics and Photovoltaics
  • Photochemistry and Electron Transfer Studies
  • Perovskite Materials and Applications
  • Molecular Junctions and Nanostructures
  • Molecular Sensors and Ion Detection
  • Analytical Chemistry and Sensors
  • Synthesis and Properties of Aromatic Compounds
  • Chemistry and Chemical Engineering
  • Conducting polymers and applications
  • Click Chemistry and Applications
  • Radical Photochemical Reactions
  • Photoreceptor and optogenetics research
  • Synthesis and Biological Evaluation
  • Quantum optics and atomic interactions
  • Advanced Memory and Neural Computing
  • Gas Sensing Nanomaterials and Sensors
  • ZnO doping and properties
  • Supramolecular Chemistry and Complexes
  • Quantum and electron transport phenomena
  • Fullerene Chemistry and Applications
  • Various Chemistry Research Topics

Northumbria University
2020-2024

Durham University
2012-2023

University of Bristol
2022

Durham Technical Community College
2017-2020

Newcastle upon Tyne Hospital
2020

University of Cambridge
2014

Abstract Knowing the underlying photophysics of thermally activated delayed fluorescence (TADF) allows proper design high efficiency organic light-emitting diodes. We have proposed a model to describe reverse intersystem crossing (rISC) in donor–acceptor charge transfer molecules, where spin–orbit coupling between singlet and triplet states is mediated by one local donor (or acceptor). This second order, vibronically coupled mechanism describes basic TADF. Through series measurements,...

10.1038/ncomms13680 article EN cc-by Nature Communications 2016-11-30

Abstract A new family of anthracene core, highly fluorescent emitters is synthesized which include diphenylamine hole transport end groups. Using a very simple one or two layer organic light emitting diode (OLED) structure, devices without outcoupling achieve an external quantum efficiency 6% and photonic efficiencies 20 cd/A. The theoretical maximum such should not exceed 3.55%. Detailed photophysical characterization shows that for these based 2T 1 ≤T n so in this special case, triplet...

10.1002/adfm.201201750 article EN Advanced Functional Materials 2012-09-24

Abstract Regio- and conformational isomerization are fundamental in chemistry, with profound effects upon physical properties, however their role excited state properties is less developed. Here two regioisomers of bis(10H-phenothiazin-10-yl)dibenzo[b,d]thiophene- S,S -dioxide, a donor–acceptor–donor (D–A–D) thermally-activated delayed fluorescence (TADF) emitter, studied. 2,8-bis(10H-phenothiazin-10-yl)dibenzo[b,d]thiophene- -dioxide exhibits only one quasi-equatorial conformer on both...

10.1038/ncomms14987 article EN cc-by Nature Communications 2017-04-13

Abstract Hyperfluorescence shows great promise for the next generation of commercially feasible blue organic light-emitting diodes, which eliminating Dexter transfer to terminal emitter triplet states is key efficiency and stability. Current devices rely on high-gap matrices prevent transfer, unfortunately leads overly complex from a fabrication standpoint. Here we introduce molecular design where ultranarrowband emitters are covalently encapsulated by insulating alkylene straps. Organic...

10.1038/s41563-024-01812-4 article EN cc-by Nature Materials 2024-03-13

Small, apolar aromatic groups, such as phenyl rings, are commonly included in the structures of fluorophores to impart hindered intramolecular rotations, leading desirable solid-state luminescence properties. However, they not normally considered take part through-space interactions that influence fluorescent output. Here, we report on photoluminescence properties a series phenyl-ring molecular rotors bearing three, five, six, and seven groups. The emissions from two found originate,...

10.1021/jacs.7b08570 article EN cc-by Journal of the American Chemical Society 2017-11-18

This review summarises the significant developments in our understanding and control of thermally-activated delayed fluorescence (TADF) molecules spin–vibronic coupling mechanism, from which we have designed new generations emitters.

10.1039/c8tc00991k article EN Journal of Materials Chemistry C 2018-01-01

We expose significant changes in the emission color of carbazole-based thermally activated delayed fluorescence (TADF) emitters that arise from presence persistent dimer states thin films and organic light-emitting diodes (OLEDs). Direct photoexcitation this state 1,2,3,5-tetrakis(carbazol-9-yl)-4,6-dicyanobenzene (4CzIPN) reveals influence species on purity its photoluminescence electroluminescence. The is sensitive to sample preparation method, enduring contributes widely reported...

10.1021/acs.jpcc.9b01458 article EN cc-by The Journal of Physical Chemistry C 2019-04-03

Understanding the excited-state dynamics and conformational relaxation in thermally activated delayed fluorescence (TADF) molecules, including conformations that potentially support intramolecular through-space charge transfer, can open new avenues for TADF molecular design as well elucidate complex photophysical pathways structurally molecules. Emissive molecules comprising a donor (triphenylamine, TPA) an acceptor (triphenyltriazine, TRZ) bridged by second...

10.1021/acs.jpcc.9b01900 article EN cc-by The Journal of Physical Chemistry C 2019-04-17

Rather than donor–acceptor dihedral angles, the TADF performance of DMAC–BZN positional isomers is instead controlled by differences in acceptor strength arising from π-system electron density – along with a through-space dipole interaction.

10.1039/c9tc02742d article EN cc-by Journal of Materials Chemistry C 2019-01-01

Herein, we expose how the antagonistic relationship between solid-state luminescence and photocyclization of oligoaryl alkene chromophores is modulated by conjugation length their alkenyl backbones. Heptaaryl cycloheptatriene molecular rotors exhibit aggregation-induced emission characteristics. We show that turned off upon breaking epoxide formation. While this modification deleterious to photoluminescence, it enables formation extended polycyclic frameworks Mallory reactions. exploit...

10.1002/anie.202202193 article EN cc-by Angewandte Chemie International Edition 2022-03-28

A new iptycene unequivocally validates homoconjugation as a viable strategy to simultaneously enhance TADF reverse intersystem crossing and radiative decay.

10.1039/d2tc00460g article EN cc-by Journal of Materials Chemistry C 2022-01-01

We report magnetoconductance measurements on polymer:fullerene photovoltaic devices in the regime of high fields and low temperatures, where spin polarization injected carriers plays an important role. The current either decreases or increases with magnetic field, depending whether interfacial charge-transfer state lies above below intramolecular triplet energy. Rapid transitions from states to lower-lying excitons constitute loss mechanism that is responsible for negative observed.

10.1063/1.4865203 article EN Applied Physics Letters 2014-02-10

Thermally activated delayed fluorescence has been found in a group of tricarbazolylamines that are purely electron-donating, non-charge-transfer (CT) molecules. We show the reverse intersystem crossing step these materials is mediated through upper triplet states. Reverse internal conversion shown to be thermally mechanism behind harvesting mechanism. The strongly mixed n−π*/π–π* character lowest energy optical transitions retains high oscillator strength and gives rise ΦPL. Organic...

10.1021/acs.jpcc.8b07610 article EN The Journal of Physical Chemistry C 2018-09-28

Emitters showing thermally activated delayed fluorescence (TADF) in electroluminescent devices rely on efficient reverse intersystem crossing (rISC) arising from small thermal activation barriers between the lowest excited triplet and singlet manifolds. A donor–acceptor compound consisting of a demethylacridine donor methylbenzoate acceptor group is used as model TADF emitter. The spectroscopic signatures this system are characterized using combination photoluminescence excitation, decay...

10.1021/acs.jpca.9b11083 article EN The Journal of Physical Chemistry A 2020-02-05

Heterocyclic dimers consisting of combinations butterfly-shaped phenothiazine (PTZ) and its chemically oxidized form phenothiazine-5,5-dioxide (PTZ(SO

10.1002/chem.202300428 article EN cc-by Chemistry - A European Journal 2023-03-14

A versatile <italic>N</italic>-alkylation strategy controls the presence of charge-transfer excited states and emission colour N-heterocyclic chromophores.

10.1039/d0sc02460k article EN cc-by Chemical Science 2020-01-01

Greater than the sum of its parts – a 3D ICT molecule displays greatly improved optoelectronic properties over 2D analogue.

10.1039/c9tc03255j article EN Journal of Materials Chemistry C 2019-01-01

In tweezer-like dinuclear platinum( ii ) complexes, the exchange of chloride ligand for thiocyanate promotes interfacial interactions, leading to low-energy emission.

10.1039/d4nj03357d article EN cc-by New Journal of Chemistry 2024-01-01

Anisotropy within three TADF materials has been observed using steady-state fluorescence polarization. This technique allowed for the observation of differences in polarization dilute solution, and both unstretched stretched films; latter producing highly aligned molecules sample. Using these films anisotropy can be between emission from 1LE 1CT states upon exciting different absorption bands. Furthermore, time-resolved measurements highlights strong vibronic coupling charge-transfer local...

10.1021/acs.jpclett.7b00729 article EN The Journal of Physical Chemistry Letters 2017-05-26

4DTPIPN has a strong tendency for dimer formation, even in dilute film, and possesses higher colour purity than 4CzIPN but this is traded-off against the photoluminescence quantum yield. (Credit to LeStudio/Shutterstock James Bond themed background.)

10.1039/d1tc04913e article EN cc-by Journal of Materials Chemistry C 2022-01-01
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