京都大学 / 0048 / 新制・課程博士 / 博士(農学) / 甲第22486号 / 農博第2390号 / 新制||農||1075(附属図書館) / 学位論文||R2||N5266(農学部図書室) / 京都大学大学院農学研究科森林科学専攻 / (主査)教授 髙野 俊幸, 教授 和田 昌久, 教授 河本 晴雄 / 学位規則第4条第1項該当 / Doctor of Agricultural Science / Kyoto University / DGAM

No description available.

Organic semiconductors (OSCs) have already been shown to have great potential to play an important role in the future of clean energy generation (organic solar cells) and provide energy efficient lighting (organic light-emitting diodes, OLED). Prior research has found that the light-emission efficiency of OLED is severely limited by the magnetic state (technically the spin-configuration) of the light-emission process. In this thesis, we work on the processes using external magnetic fields that can overcome these magnetic limitations. A major focus of this research is to enhance the performance of OLED, while at the same time to unravel the scientific mechanisms by which magnetic fields act on OSCs devices. Thermally activated delayed fluorescence (TADF) is a next-generation OLED emission technology which enables nearly 100% light-emission efficiency without using heavy precious metals. TADF characteristics depend on the probability of reverse intersystem crossing (RISC) from the triplet excited states (T1) to singlet excited states (S1). The conversion (T1 to S1) process depends strongly on spin dynamics, thus we predict a dramatic magnetic field effects (MFEs) in such TADF OLED devices. In subsequent experiments we observed that changes in TADF devices due to various forms of electrical stress can lead to enormous increases in magnetic field effects (MFEs) on the current (> 1400%) and electroluminescence (> 4000%). Our work provides a flexible and inexpensive pathway towards magnetic functionality and field sensitivity in current organic devices. Such OLED pave the way for novel magnetic sensitive OSCs devices with integrated optical, electronic and magnetic characteristics. Organic magnetoresistance (OMAR) has been observed to alter the current and efficiency of OLED without any ferromagnetic components. Here we utilizes slight alterations to the device properties, the addition of a radical-doped functional layer, in which the spin-relaxing effects of localized nuclear spins and electronic spins interfere, to address the assumption about the importance of the hyperfine interaction and to attempt to differentiate between the different models for OMAR. A feature where the magnitude of OMAR exhibits a plateau over a wide range of doping fraction was observed at all temperatures investigated. This phenomenon is well explained by a theory in which a single dopant spin strongly interacts, by exchange, with one of the bottleneck sites. A similar can be used to explain the efficiency increases observed in organic solar cells for certain doping fractions.

Thermally activated delayed fluorescence (TADF) has been proposed as a pathway to achieve high efficiency organic light-emitting diodes (OLEDs) without the use of heavy metal atoms in molecular structures. Many different factors can be decisive for efficient light emission from TADF emitters. However, a complete picture of the working mechanisms behind TADF is still missing and further research exploring novel material and device ideas is required. This thesis aims to extend the understanding of TADF emitter and OLED design considerations by investigating photophysical properties of novel materials as well as fabricating, optimizing and characterizing devices. TADF emitters have great potential of being used in OLEDs because they allow for high quantum efficiencies by utilizing triplet states via reverse intersystem crossing (RISC). In small molecules this is done by spatially separating the frontier orbitals, forming an intramolecular charge-transfer state (iCT) and leading to a small energy difference between lowest excited singlet and triplet states (Δ𝐸ST). In polymer emitters, sufficient frontier orbital separation is harder to achieve, and typical strategies usually include adding known TADF units as sidechains onto a polymer backbone. In this thesis, a novel pathway of TADF polymer design is explored. A shift from a non-TADF monomer to TADF oligomers is explored. The monomer shows non-TADF emission and the delayed emission is shown to be of triplet-triplet annihilation (TTA) origin. An iCT state is formed already in the dimer, leading to a much more efficient TADF emission. This is confirmed by an almost two-fold increase of photoluminescence quantum yield (PLQY), a decrease in the delayed luminescence lifetime and the respective spectral line shapes of the molecules. Recently, intermolecular effects between small-molecule TADF emitters have been given more attention, revealing strong solid-state solvation or aggregation induced changes of sample performance. Implications of this on device performance are not yet fully covered. A thorough investigation of a novel TADF emitter 5CzCO2Me is conducted. Steady-state emission spectra reveal a luminescence redshift with increasing emitter concentration in a small molecule host. In all investigated concentrations, the emission profile remains the same, thus the redshift is attributed to the solid-state solvation effect. The highest photoluminescence quantum yield (PLQY) is achieved in the 20 wt% sample, reaching 66 %. The best OLED in terms of current-voltage-luminance and external quantum efficiency parameters is the device with 60 wt% emitter concentration, reaching maximal EQE values of 7.5 %. It is shown that the emitter transports holes and that charge carrier recombination does not take place on the bandgap of the host, but rather, a mixed host-guest concentration dependent recombination is seen. The hole transporting properties of 5CzCO2Me allows for a new dimension in tuning the device performance by controlling the emitter concentration.

Ein vielversprechendes Design für organische lichtemittierende Dioden (OLEDs) verwendet eine Wirt-Gast-Strategie durch Dispergieren einer kleinen Menge eines hocheffizienten Emitters (der Gast) in eine passende Transportmatrix (der Wirt). Die Aufgabe des Wirts ist den Exzitonentranport zum Emitter sicherzustellen und den Zerfall von Triplet-Exzitonen zu verhindern, und damit eine hohe Bauteilperformance zu erreichen. Die vorliegende Arbeit konzentriert sich auf die Beziehung zwischen Molekülstruktur und optoelektrischer Eigenschaften von Carbazol/Dibenzothiophen-Derivaten. Die Untersuchung umfasst sieben dieser Derivate für den Wirt, bei denen die Carbazoleinheit als Donator und die Dibenzothiopheneinheit als Akzeptor fungiert, wobei beide durch einen oder mehrere Phenylabstandshalter verbunden sind. Diese Wahl der Wirtsmaterialien erlaubt es den Einfluss der erweiterten Phenylabstandshalter und der unterschiedlichen molaren Verhältnisse von Akzeptor zu Donator zu untersuchen. Es ergab sich, dass eine kürzere Phenylabstandshalterlänge die Bauteilperformance durch eine größere Löcher- und Elektronendichte in der Emitterschicht verbessert; und ein 1:1 Carbazol-zu-Dibenzothiophen-Verhältnis der Bauteilperformance zuträglich ist, da es zu einem Ladungsträgergleichgewicht in der Emitterschicht führt. Diese Arbeit zeigt, unter Verwendung dieser Wirtsmaterialien, blaue FIrpic-basierte phosphoreszierende OLEDs (PhOLEDs) und grüne 4CzIPN-basierte thermisch aktivierte verzögerte Phosphoreszenz (TADF) OLEDs. Die blauen PhOLEDs und grünen TADF OLEDs mit mDCP zeigten Effizienzen von 43 cd/A (18.6%) beziehungsweise 66 cd/A (21%). / A particularly interesting organic light-emitting diodes (OLEDs) design adopts a host-guest strategy by dispersing a small amount of highly efficient emitter (the guest) into an appropriate transport matrix (the host). The host is utilized to transfer excitons to the emitter and to prevent triplet exciton quenching, thus high device performance can be achieved. The present thesis focuses on the relationship between the molecular structure and opto-electrical properties of carbazole/dibenzothiophene derivatives. The investigation encompasses seven of these derivatives for the host, in which the carbazole unit acts as a donor and the dibenzothiophene as an acceptor while they are linked through phenyl spacer(s). This choice of host materials enables to assess the impact of extended phenyl spacers and different acceptor to donor molar ratios. It was found that decreasing the phenyl spacer length enhances the device performance due to the larger both hole and electron densities in the emitting layer; and a 1:1 carbazole to dibenzothiophene ratio is favorable for device performance, since it balances the charge carriers in the emitting layer. Using these host materials, the work presented in this thesis demonstrates high-performance blue FIrpic-based phosphorescent OLEDs (PhOLEDs) and green 4CzIPN-based thermally activated delayed fluorescence (TADF) OLEDs. The blue PhOLEDs and green TADF OLEDs with mDCP showed efficiencies of 43 cd/A (18.6%) and 66 cd/A (21%), respectively.

Maleimide based highly luminescent material Cbz-MI with donor acceptor donor (D-A-D) backbone has been synthesized and characterized. An organic light emitting diode fabricated using this material as emitting layer exhibited EQE of 2.5% in the yellow region of visible spectrum. Due to the small energy gap of materials emitting in this region of spectrum, EQE of OLED is usually limited by various non-radiative decays and high EQE of OLED using this material proves that most of the nonradiative decay pathways have been avoided by the careful design of molecule and device structure. Although Cbz-MI did not show TADF properties, but if tailored with right electron donor along with maleimide as an acceptor, such derivatives may exhibit TADF properties

No description available.

As the third generation of luminescent materials, thermally activated delayed fluorescence (TADF)-type compounds have great potential as emitter molecules in OLEDs allowing for electro-fluorescence with 100 % internal quantum efficiency. For organic electronics, the general wide range of applications from OLEDs, bio-fluorescence imaging to sensor technologies and photonic energy storages roots on the enormous variety of organic materials. Especially in the field of metal- free aromatic designs, the range of possible materials showing diverse triplet harvesting effects is immense, making material development a highly complex task. Firstly, initial efforts in the understanding of the basic concepts behind TADF will be highlighted. A rational design strategy for TADF materials will be illustrated on an innovative material series based on phenylcarbazoles. A reasonable branch of isomers are theoretically constructed and slight stoichiometric modifications are performed to understand how molecular structure and intramolecular steric hindrance affects reverse intersystem crossing (RISC), while simultaneously revealing the strategy for deep blue TADF. The rational design of a bluish green TADF material called 5CzCF3Ph providing CIEy ≤ 0.4 is demonstrated, enabling peak EQE values of 12.1 % with a promising LT50 of 2 hrs at 500 cd∙m-2. Subsequently, the photophysics of five newly designed trimeric donor (D)-acceptor (A)-donor (D) type material compounds, analogue concepts to archetypical TADF designs, highlight the importance of intramolecular electronic couplings between adjacent triplet states for adiabatically-driven TADF, revealing the mechanism of local type triplet state perturbations on 3CT states. The most promising candidate (DMAC-PTO-DMAC) is disclosed and in turn optimized to meet required conditions for deep blue TADF emission. Ultimately, a deep blue luminescent material called isoDMAC-PTO is developed, featuring CIE coordinates of (0.16, 0.14) with an overall quantum yield of (86.4 ± 0.5) %. The focus switches to the fundamental understanding of the underlying mechanism giving rise to TADF in small molecules, leaving the scope of deep blue emission. While investigating the photophysical properties of a synthesized donor (D)-acceptor (A) type thermally activated delayed fluorescence (TADF) emitter named methyl 2-(9,9-dimethylacridin-10-yl)benzoate (DMAC-MB), it is possible to identify the excited state dynamics mediating the spin-flip process and hence the reutilization of non-radiative triplet states allowing for an internal quantum efficiency approaching unity. As experimentally observed by detailed temperature- and time-dependent transient photoluminescence (PL) measurements and consolidated by comprehensive quantum-chemical considerations, excited state configuration interaction by non-adiabatic couplings are anticipated as key property behind triplet up-conversion in the vicinity of conical intersections, contributing to recent research facing the exciton management within the auspicious field of TADF. For the first time, this thesis reports that even a TADF-silent molecule can be converted into efficient TADF systems by increasing the donor π- conjugation length through polymerization of the building block itself. With a total photoluminescence quantum yield up to 71 %, comprehensible research illustrates an efficient thermally activated delayed fluorescence polymer P1, based solely on non-TADF chromophores represented by a model compound 2 (PLQY of 3 % at RT). Finally, as predicted by TDDFT calculations and shown for the first time in the aspiring field of TADF, a thermally activated delayed fluorescence polymer based on a merely radiative, solely phosphorescent repeating unit is demonstrated. Intramolecular π-conjugation is exploited to trigger the charge-transfer excited state energy, revealing a general design tool to provoke TADF, reserved in particular for polymers. While the introduced twisted methyl 2-(9,9-dimethylacridin-10-yl) benzoate (DMAC-MB) reveals efficient thermally activated delayed fluorescence (TADF), a modified analogue 9,9-Dimethyl-5H,9H-quinolino[3,2,1-de]acridin-5-one (DMAC-ACR) shows emerging room temperature phosphorescence (RTP). As for TADF, intramolecular non-adiabatic couplings are unlocked as key feature actuating persistent RTP, linking photophysical analogies between TADF and RTP to structural self-similarities. Last but not least, degradation processes in TADF materials will be addressed. A correlation between theoretically calculated bond-dissociation energies (BDEs) and phenomenological observations reveals that low BDEs, in particular along pronounced charge-transfer bonds, ultimately lead to irreversible TADF material degradation induced by bi-molecular processes comprising TPQ as well as TTA. Finally, this thesis reveals the photophysics of 24 newly designed, synthesized and characterized TADF materials and demonstrates a fundamentally new approach for RTP, based on structural analogues to TADF. Far reaching design principles as conjugation induced TADF in polymers, as well as new design strategies selectively incorporating virbonic couplings yield device performances comprising LT50 of 2 hrs at 500 cd∙m-2 and targeted deep blue emission with CIE (0.16, 0.14). While lighting the way for TADF as future luminescent OLED materials, intrinsic material instabilities due to low bond-dissociation energies are disclosed as key-issues for tomorrows research.