We demonstrated that the open-circuit voltage (V) of rubrene/C organic photovoltaic (OPV) devices can be substantially improved by changing the rubrene thickness. A shoulder exhibited in a range of 500-550 nm was observed. This result indicated that the singlet excitons of rubrene were increased when the thickness of the rubrene layer was increased. Capacitance-voltage measurements were conducted for estimating the built-in potential of the devices. The calculated V was higher than that of the experiment, thus indicating that energetic losses occurred in the devices. We reused the reciprocity and revised Marcus theory for determining the charge-transfer (CT) properties of the devices. The CT properties of the CT states at the rubrene/C interface remained similar. The nonradiative energetic losses become smaller when the rubrene layer was increased, thus indicating the bimolecular recombination was increased. The increased recombination thermally activated the electrons in C into rubrene for forming the singlet excitons in rubrene. The reduction in reorganization energy indicated that the electroluminescence of rubrene was enhanced, thereby improving V. These results proved that the two-step thermal activation of C electrons and the improved V of rubrene were caused by the increased singlet excitons of rubrene.
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http://dx.doi.org/10.1021/acsami.6b08363 | DOI Listing |
Chem Commun (Camb)
December 2024
Department of Chemistry, Indian Institute of Science Education and Research (IISER), Pune (411008), Maharashtra, India.
In this study, we investigated the aggregation-induced delayed fluorescence (AIDF) properties of three luminogens - TN, TA, and TP. Our comprehensive theoretical analysis reveals a significant reduction in the Δ in their aggregated or solid-state, activating TADF, on a ∼μs time-scale. Additionally, these luminogens demonstrate two-photon excited anti-Stokes photoluminescence emission and improved photocurrent generation, attributed to their strong charge transfer characteristics and longer singlet exciton lifetimes.
View Article and Find Full Text PDFAdv Mater
December 2024
Research Laboratory of Electronics, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, MA, 02139, USA.
Singlet exciton fission has the potential to increase the efficiency of crystalline silicon solar cells beyond the conventional single junction limit. Perhaps the largest obstacle to achieving this enhancement is uncertainty about energy coupling mechanisms at the interfaces between silicon and exciton fission materials such as tetracene. Here, the previously reported silicon-hafnium oxynitride-tetracene structure is studied and a combination of magnetic-field-dependent silicon photoluminescence measurements and density functional theory calculations is used to probe the influence of the interlayer composition on the triplet transfer process across the hafnium oxynitride interlayer.
View Article and Find Full Text PDFJ Am Chem Soc
December 2024
Department of Chemistry and Paula M. Trienens Institute for Sustainability and Energy, Northwestern University, Evanston, Illinois 60208-3113, United States.
Singlet exciton fission (SF) and symmetry-breaking charge separation (SB-CS) are both photophysical processes that can occur between two organic chromophores and are both of interest to improve solar energy conversion. Here, we tuned the photophysics of a 9,9'-bianthracene () single crystal between SF and SB-CS using solvent intercalation to change the electric field within the crystal. Crystals of were grown in -xylene, chlorobenzene, -dichlorobenzene, and benzonitrile, as well as solvent-free from a melt.
View Article and Find Full Text PDFSpectrochim Acta A Mol Biomol Spectrosc
December 2024
Henan Key Laboratory of Infrared Materials & Spectrum Measures and Applications, School of Physics, Henan Normal University, 46# East of Construction Road, Xinxiang 453007, Henan, China; Institute of Physics, Henan Academy of Sciences, Zhengzhou 450046, Henan, China. Electronic address:
The para-linked carbazole-biphenyl (CBP) is commonly utilized in phosphorescent organic light-emitting diodes. This study investigates the steric hindrance and heavy-atom effects in CBP derivatives through transient absorption spectroscopy. In contrast to CBP, CBP derivatives shows new triplet-triplet absorption signals and isosbestic points, accompanied by the decay of excited state absorption signal, which indicates the occurrence of intersystem crossing (ISC).
View Article and Find Full Text PDFChem Sci
December 2024
Université Paris-Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell (I2BC) Gif-sur-Yvette 91190 France
[This corrects the article DOI: 10.1039/D4SC04732J.].
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