PRZEMYSŁAW DATA / RESEARCH

Research

Photophysical and electrochemical processes in organic semiconductors.

My research examines the relationship between molecular structure, excited-state dynamics and device performance. Experimental spectroscopy and electrochemistry connect the properties of individual molecules with their behaviour in thin films and electronic devices.

01 / PHOTOPHYSICS

Excited-state dynamics

Thermally activated delayed fluorescence (TADF), room-temperature phosphorescence (RTP) and charge-transfer states in organic materials. The focus is on the mechanisms that govern emission and non-radiative decay.

02 / ELECTROCHEMISTRY

Electronic structure and redox processes

Electrochemical and spectroelectrochemical characterisation of conjugated molecules and polymers, including the relationship between redox behaviour and the properties of optoelectronic active layers.

03 / ORGANIC ELECTRONICS

Materials for OLEDs

Development and characterisation of organic emitters, exciplex systems and hyperfluorescent materials. Connecting photophysical mechanisms with electroluminescence and device efficiency.

04 / EMERGING DIRECTIONS

Organic energy materials

Research interests extend to organic thermoelectrics, redox-active storage interfaces and coupled light–heat–charge processes. These directions build on existing expertise in spectroscopy, electrochemistry and organic electronic materials.

Experimental methods

Electrochemistry and spectroelectrochemistry; steady-state and time-resolved spectroscopy; thin-film preparation; OLED fabrication and characterisation.

EXCITED-STATE PHOTOPHYSICS

Thermally activated delayed fluorescence

Thermal energy enables reverse intersystem crossing (RISC) from T₁ to S₁. Fluorescence then occurs from S₁ to S₀.

Simplified scheme · selected pathways · not to scale.
Mechanism reference

Simplified TADF energy-level scheme Energy increases upwards. The excited singlet S1 lies above the triplet T1. Intersystem crossing connects S1 to T1. Thermally activated reverse intersystem crossing returns the population from T1 to S1, followed by fluorescence from S1 to the ground state S0. Only selected pathways are shown; the scheme is not to scale. S₁ T₁ S₀ RISC ISC ΔEST Energy