Dominik Madea
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Dominik Madea has a total of 12 co-authors. Here are the top co-authors by number of shared publications:
- Kaede Kawaguchi
Organic Optoelectronics Unit Okinawa Institute of Science and Technology Graduate University (OIST) Onna‐son Okinawa Japan
2 shared publications - Ryoko Oyama
Division of Materials Science Nara Institute of Science and Technology (NAIST) Nara Japan
2 shared publications - Ryota Kabe
Organic Optoelectronics Unit, Okinawa Institute of Science and Technology Graduate University, 1919-1 Tancha, Onna-son, Okinawa 904-0495, Japan
2 shared publications - Yemineni S. L. V. Narayana
Okinawa Institute of Science and Technology Graduate University
2 shared publications Amal Jose
Organic Optoelectronics Unit, Okinawa Institute of Science and Technology Graduate University, 1919-1 Tancha, Onna-son, Okinawa 904-0495, Japan
1 shared publication- Amal Jose
Okinawa Institute of Science and Technology Graduate University
1 shared publication
Latest Publications
- Open Access
- 5 December 2025
- Published by American Association for the Advancement of Science (AAAS) in Science Advances
- Vol. 11 (49) , eadx9806
Investigating charge accumulation mechanisms in organic materials via slow transient emission spectroscopy
Long-persistent luminescent (LPL) materials store photon energy as charges and emit light over extended periods via charge recombination. LPL decay typically follows a power law rather than an exponential decay, enabling confirmation of charge accumulation from emission decay characteristics. While charge generation in organic materials has been widely studied at donor-acceptor (D/A) interfaces, it remains underexplored in single-component luminescent materials. Here, we investigate charge generation in organic solids by dispersing a luminescent molecule in various hosts and performing slow transient emission analyses. This approach enables the evaluation of ionization through accumulated triplet excited states and the detection of weak charge accumulation, which are difficult to capture using conventional transient techniques. Our results show that ionization in single-component materials proceeds through resonance-enhanced multiphoton ionization, although it is less efficient than at D/A interfaces. This approach provides insight into long-term photophysical and photochemical processes such as photodegradation.
- 5 December 2025
- Published by American Association for the Advancement of Science (AAAS) in Science Advances
- Vol. 11 (49) , eadx9806
Open AccessInvestigating charge accumulation mechanisms in organic materials via slow transient emission spectroscopy
Long-persistent luminescent (LPL) materials store photon energy as charges and emit light over extended periods via charge recombination. LPL decay typically follows a power law rather than an exponential decay, enabling confirmation of charge accumulation from emission decay characteristics. While charge generation in organic materials has been widely studied at donor-acceptor (D/A) interfaces, it remains underexplored in single-component luminescent materials. Here, we investigate charge generation in organic solids by dispersing a luminescent molecule in various hosts and performing slow transient emission analyses. This approach enables the evaluation of ionization through accumulated triplet excited states and the detection of weak charge accumulation, which are difficult to capture using conventional transient techniques. Our results show that ionization in single-component materials proceeds through resonance-enhanced multiphoton ionization, although it is less efficient than at D/A interfaces. This approach provides insight into long-term photophysical and photochemical processes such as photodegradation.
- Open Access
- 6 February 2025
- Published by American Chemical Society (ACS) in ChemRxiv
Revealing Charge Accumulation Mechanisms in Organic Materials via Slow Transient Emission Spectroscopy
Long-persistent luminescent (LPL) materials store photon energy as charge and emit light over extended periods due to charge recombination. The LPL decay profiles follow a power-law rather than an exponential decay, enabling the confirmation of charge accumulation from the emission decay characteristics. While charge generation in organic materials has primarily been discussed in the context of photo-induced charge separation at electron donor-acceptor (D/A) interfaces, charge generation in single-component luminescent materials has not been extensively addressed. Here, we investigated the mechanism of charge generation in organic solids by dispersing the same luminescent material in various host media and performing slow transient emission analyses. This approach allowed us to evaluate ionization through accumulated triplet excited states and detect extremely weak charge accumulation, which is challenging with conventional transient analyses.
- 6 February 2025
- Published by American Chemical Society (ACS) in ChemRxiv
Open AccessRevealing Charge Accumulation Mechanisms in Organic Materials via Slow Transient Emission Spectroscopy
Long-persistent luminescent (LPL) materials store photon energy as charge and emit light over extended periods due to charge recombination. The LPL decay profiles follow a power-law rather than an exponential decay, enabling the confirmation of charge accumulation from the emission decay characteristics. While charge generation in organic materials has primarily been discussed in the context of photo-induced charge separation at electron donor-acceptor (D/A) interfaces, charge generation in single-component luminescent materials has not been extensively addressed. Here, we investigated the mechanism of charge generation in organic solids by dispersing the same luminescent material in various host media and performing slow transient emission analyses. This approach allowed us to evaluate ionization through accumulated triplet excited states and detect extremely weak charge accumulation, which is challenging with conventional transient analyses.