Rubrene

The crystal structures of two rubrene derivatives, 5,11-diphenyl-6,12-bis-[4-(tri-fluoro-meth-yl)phen-yl]tetra-cene, C44 H26 F6 , and 5,11-bis-(4- tert -butyl-phen-yl)-6,12-di-phenyl-tetra-cene, C50 H44 , are presented. Each are substituted on diagonal (5/11) phenyl rings. Each derivative has one polymorph reported previously. A discussion of the differences between each derivative and its previously reported polymorph is provided. The triclinic packing of the CF3 -substituted structure is similar to the packing of the parent rubrene's triclinic polymorph...

Triplet-triplet annihilation photon upconversion (TTA-UC) has received significant attention in energy harvesting applications such as solar cells. The realization of high upconversion (UC) performance in the form of films is a crucial factor for the incorporation of this technology into large-area devices. Herein, we propose a porous UC film prepared by an emulsification method with a poly(vinyl alcohol) (PVA) aqueous solution and a toluene solution of chromophores (rubrene/Pd-tetraphenyltetraanthraporphyrin pair) that achieved considerable UC performance in the near-infrared (NIR) (810 nm) to visible (560 nm) range with a maximum quantum yield of 3...

Halide perovskite-based photon upconverters utilize perovskite thin films to sensitize triplet exciton formation in a small-molecule layer, driving triplet-triplet annihilation upconversion. Despite having excellent carrier mobility, these systems suffer from inefficient triplet formation at the perovskite/annihilator interface. We studied triplet formation in formamidinium-methylammonium lead iodide/rubrene bilayers using photoluminescence and surface photovoltage methods. By studying systems constructed on glass as well as hole-selective substrates, comprising self-assembled layers of the carbazole derivative 2PACz ([2-(9H-carbazol-9-yl)ethyl]phosphonic acid) on indium-doped tin oxide, we saw how changes in the carrier dynamics induced by the hole-selective substrate perturbed triplet formation at the perovskite/rubrene interface...

Two-dimensional (2D) Ruddlesden-Popper (RP) metal halide perovskites have emerged as a promising material for X-ray detection. However, defects and ion migration generated nonradiative recombination and high dark current could cause severe performance degradation, which hinders their application. Herein, rubrene was added to the precursor solution of BA2 MA3 Pb4 I13 to modulate the performance of the 2D RP perovskite X-ray detectors. The cation-π interaction between rubrene and perovskite could passivate the defects and inhibit the ion migration, resulting in improved performance and stability...

Transfer integral is a crucial parameter that determines the charge mobility of organic semiconductors, and it is very sensitive to molecular packing motifs. The quantum chemical calculation of transfer integrals for all the molecular pairs in organic materials is usually an unaffordable task; fortunately, it can be accelerated by the data-driven machine learning method now. In this work, we develop machine learning models based on artificial neutral networks to predict transfer integrals accurately and efficiently for four typical organic semiconductor molecules: quadruple thiophene (QT), pentacene, rubrene, and dinaphtho[2,3-b:2',3'-f]thieno[3,2-b]thiophene (DNTT)...

Recent progress in organic electronics has attracted interest due to their excellent characteristics that include photovoltaic, light emission, and semiconducting behaviours. Spin-induced properties play important roles in organic electronics, while introducing spin into an organic layer in which spin responses, such as a weak spin-orbital coupling and long spin-relaxation time, allows a variety of spintronic applications to be achieved. However, such spin responses are rapidly attenuated by misalignment in the electronic structure of hybrid structures...

Describing charge carrier anisotropy in crystalline organic semiconductors with ab initio methods is challenging because of the weak intermolecular interactions that lead to both localized and delocalized charge transport mechanisms. Small polaron hopping models (localized) are generally used to describe materials with small charge carrier mobilities, while periodic band models (delocalized) are used to describe materials with high charge carrier mobilities. Here, we prove the advantage of applying the constant relaxation time approximation of the Boltzmann transport equation (BTE) to efficiently predict the anisotropic hole mobilities of several unsubstituted (anthracene, tetracene, pentacene, and hexacene) and substituted (2,6-diphenylanthracene, rubrene, and TIPS-pentacene) high-mobility n-acene single crystals...

Quantum dynamics (QD) simulation is a powerful tool for interpreting ultrafast spectroscopy experiments and unraveling their microscopic mechanism in out-of-equilibrium excited state behaviors in various chemical, biological, and material systems. Although state-of-the-art numerical QD approaches such as the time-dependent density matrix renormalization group (TD-DMRG) already greatly extended the solvable system size of general linearly coupled exciton-phonon models with up to a few hundred phonon modes, the accurate simulation of larger system sizes or strong system-environment interactions is still computationally highly challenging...

Perovskite-sensitized triplet-triplet annihilation (TTA) upconversion (UC) holds potential for practical applications of solid-state UC ranging from photovoltaics to sensing and imaging technologies. As the triplet sensitizer, the underlying perovskite properties heavily influence the generation of spin-triplet states once interfaced with the organic annihilator molecule, typically polyacene derivatives. Presently, most reported perovskite TTA-UC systems have utilized rubrene doped with ∼1% dibenzotetraphenylperiflanthene (RubDBP) as the annihilator/emitter species...

Among a large variety of organic semiconducting materials, rubrene (5,6,11,12-tetraphenyltetracene) represents one of the most prominent molecular entities mainly because of its unusually high carrier mobility. Toward finding superior rubrene-based organic semiconductors, several synthetic strategies for related molecules have been established. However, despite its outstanding properties and significant attention in the field of materials science, late-stage functionalizations of rubrene remains undeveloped, thereby limiting the accessible chemical space of rubrene-based materials...

Quantum dot-organic semiconductor hybrid materials are gaining increasing attention as spin mixers for applications ranging from solar harvesting to spin memories. Triplet energy transfer between the inorganic quantum dot (QD) and organic semiconductor is a key step to understand in order to develop these applications. Here we report on the triplet energy transfer from PbS QDs to four energetically and structurally similar tetracene ligands. Even with similar ligands we find that the triplet energy transfer dynamics can vary significantly...

Semi-experimental gas-phase structures of anthracene and rubrene (5,6,11,12-tetraphenyltetracene) were determined by means of gas electron diffraction (GED). The use of the flexible restraints in the refinement of the GED data successfully resolves non-equivalent C-C bond lengths. The tetracene core of an isolated rubrene molecule was found to exhibit a twist distortion of about 18°; this is less than DFT calculations predict (30-40°). The modified Feller-Peterson-Dixon method in conjunction with high-level DLPNO-CCSD(T) calculations was employed to resolve the discrepancy between the available experimental gas-phase enthalpies of formation for rubrene...

Transient chemistry of sensitizing dyes is important to obtain insights into the photochemical conversion processes of light harvesting assemblies. We have now employed transient absorption spectroscopy (pulsed laser and pulse radiolysis) to characterize the excited state and radical intermediates of a perylene derivative, (5,10,15,20-Tetraphenylbisbenz[5,6]indeno[1,2,3- cd :1',2',3'- lm ]perylene (DBP). The distinguishable transient absorption features for the singlet and triplet excited states and radical anion and radical cation provide spectral fingerprints to identify the reaction intermediates in photochemical energy and electron transfer processes of composite systems involving DBP...

One of the major limitations of solid-state perovskite-sensitized photon upconversion to date is that the only annihilator successfully paired with the perovskite sensitizer has been rubrene, raising the question of whether this appraoch of triplet sensitization is universal or limited in scope. Additionally, the inherent energetic mismatch between the perovskite bandgap and the rubrene triplet energy has restricted the apparent anti-Stokes shift achievable in the upconversion process. To increase the apparent anti-Stokes shift for upconversion processes, anthracene derivates are of particular interest due to their higher triplet energies...

Epitaxial growth, often termed "epitaxy", is one of the most essential techniques underpinning semiconductor electronics, because crystallinities of the materials seriously dominate operation efficiencies of the electronic devices such as power gain/consumption, response speed, heat loss, and so on. In contrast to already well-established epitaxial growth methodologies for inorganic (covalent or ionic) semiconductors, studies on inter-molecular (van der Waals) epitaxy for organic semiconductors is still in the initial stage...

Triplet and singlet exciton diffusion plays a decisive role in triplet-triplet annihilation (TTA) and singlet fission (SF) processes of rubrene (Rub) films at low excitation power, and therefore has an important implication for TTA-mediated photon upconversion (UC). Although triplet diffusion in crystalline Rub was studied before, there is no quantitative data on diffusion in disordered Rub films most widely employed for NIR-to-Vis UC. The lack of these data hinders the progress of TTA-UC applications relying on a Rub annihilator (emitter)...

Singlet fission is detrimental to NIR-to-vis photon upconversion in the solid rubrene (Rub) films, as it diminishes photoluminescence efficiency. Previous studies have shown that thermally activated triplet energy transport drives singlet fission with nearly 100% efficiency in closely packed Rub crystals. Here, we examine triplet separation and recombination as a function of intermolecular distance in the crystalline films of Rub and the t -butyl substituted rubrene ( t BRub) derivative. The increased intermolecular distance and altered molecular packing in t BRub films cause suppressed singlet dissociation into free triplets due to slower triplet energy transport...

The ability to manipulate low-energy triplet excited states into higher-energy emissive singlet states, a process known as photon upconversion (UC), has potential applications in bioimaging, photocatalysis, and in increasing the efficiency of solar cells. However, the overall UC mechanism is complex and can involve many intermediate states, especially when semiconductors such as lead halide perovskites are used to sensitize the required triplet states. Using a combination of pulse radiolytic and electrochemical techniques, we have now explored the transient features of rubrene─a commonly employed triplet annihilator in UC systems...

In spite of the DNA walkers executing the signal accumulation task in the process of moving along the predetermined paths, the enhancement of walking dynamics and walking path controllability are still challenging due to the unprogrammed arrangements of DNA orbits. Taking these dilemmas into account, a bipedal DNA walker was designed skillfully by the virtue of wireframe orbits assembled by DNA cubes in order, which improved the efficiency and the continuity of walking. It could be attributed to the fact that both the contact chance and the dynamic interaction between walking strands and designated orbits were beneficial to minimize the possibility of derailment and improve the accumulation of signal...

Devices made using thin-film semiconductors have attracted much interest recently owing to new application possibilities. Among materials systems suitable for thin-film electronics, organic semiconductors are of particular interest; their low cost, biocompatible carbon-based materials and deposition by simple techniques such as evaporation or printing enable organic semiconductor devices to be used for ubiquitous electronics, such as those used on or in the human body or on clothing and packages1-3 . The potential of organic electronics can be leveraged only if the performance of organic transistors is improved markedly...