Organic Electronics最新文献

Transparent organic photovoltaic (TOPV) cells integrated into windows are key to reducing the carbon dioxide emissions associated with the building sector. However, TOPV cells that reach a compromise between efficiency and transparency must still be developed. In addition, to implement this technology in glass production companies, the materials and processes used in TOPV cell development must be compatible with producing these devices on an industrial scale. Here, an infrared (IR) cell combining a PC₆₀BM-based active material, ITO/ZnO as the back transparent electrode, PEDOT:PSS and ITO or Ag as the top transparent electrode, and a DBR as an antireflective coating was developed and applied on 625 mm² glass samples. The structure of the DBR based on titanium dioxide (TiO₂) and silicon dioxide (SiO₂) monolayers was adjusted to the IR cell absorption spectra to reach a power conversion efficiency (PCE) of 5 and 4.3, and an average visible transmission (AVT) of 41 % and 51 % for ITO and Ag top electrodes, respectively. The manufacturing route of these devices involved commercial polymers and coatings that can be deposited by technologies already applied in the glass industry, such as magnetron sputtering or thermal evaporation. Therefore, the IR cells developed here showed a good compromise between efficiency, transparency, and large-scale production manufacturability.

This study presents the design, synthesis, and comprehensive theoretical and photophysical analysis of two new D₃-A type thermally activated delayed fluorescence (TADF) emitters for organic light-emitting diode (OLED) applications. Utilizing a triarylboron core as the electron-accepting group and phenothiazine (PTZ) or phenoselenazine (PSZ) as electron-donating units, the molecules BTP-S and BTP-Se were developed. The D₃-A structure supports the separation of frontier molecular orbitals (FMOs), leading to minimized singlet-triplet energy gaps (ΔE_ST), which are crucial for the TADF mechanism. Density functional theory (DFT) calculations presented that BTP-S and BTP-Se exhibit band gaps (E_g) of 2.52 and 3.23 eV, respectively, with BTP-S showing an ΔE_ST value as low as 0.007 eV for the S₁-T₁ transition at the lowest energy conformation. Photophysical studies revealed high photoluminescence quantum yields (PLQYs) for both compounds, with BTP-S achieving up to 85 % in mCP films and BTP-Se up to 59 %. In vacuum-processed OLEDs, BTP-S achieved a maximum external quantum efficiency (EQE) of 25.3 %, a current efficiency (ηc) of 195.8 cd/A, and a maximum luminance (Lmax) of 17356 cd/m², while BTP-Se reached an EQE of 7.5 %, an ηc of 132.19 cd/A, and an Lmax of 16826 cd/m² likely limited by the contributions of a folded-donor conformer enabled by the Se substitution. These findings underscore the impact of donor unit selection and conformation on the TADF characteristics, and provide valuable insights for designing high-performance OLED materials.

Because of the energy gap law, as well as the spin-forbidden nature of triplet formation and transformation, it remains formidable task to achieve efficient and long-lived organic afterglow materials with long emission wavelengths, especially in the near-infrared region, under ambient conditions. Here we incorporate TADF-type afterglow mechanism in dopant-matrix systems which features a moderate k_RISC of 10¹-10² s⁻¹ to harvest triplet energies, boost afterglow efficiency and maintain afterglow lifetime. Specifically, we design a series of boron difluoride curcuminoid (CurBF₂) compounds to serve as luminescent dopants. Organic matrices of crystalline nature and with carbonyl groups are selected to suppress triplet quenching by their rigid microenvironment and populate triplet states via dipole effect developed in our group. The resultant dopant-matrix systems display near-infrared TADF-type organic afterglow with emission wavelength >700 nm, quantum yield around 10 % and afterglow lifetime >10 ms, which can function as deep-penetrating and background-independent bioimaging probes.

There inevitably appear dead zones in organic thin films fabricated by sheet-to-sheet slot-die coating because a coating start varies and the recovery time of internal pressure in slot-die head differs for each coating, resulting in poor coating repeatability. Slot-coated thin films within dead zones are thinner or thicker, possibly causing non-uniform light emission from solution-processable organic light-emitting diodes (OLEDs). To tackle it, we have devised an automatic coating start method based on the monitoring of meniscus formation. It automatically starts coatings when the cross-sectional area of meniscus reaches a certain optimal value in such a way that the start of each coating is kept unchanged. It is found that high-viscosity (4800 cPs) polydimethylsiloxane (PDMS) requires a longer time for the internal pressure of slot-die head to reach a steady state than low-viscosity (80 cPs) poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS). It can be reduced to a great extent by applying a method of discharging the solution in advance (pre-discharging scheme). Compared with high-viscosity PDMS films, low-viscosity PEDOT:PSS films are shown to have longer dead zones and poorer repeatability due to the fact that the dead zone of relatively thin films varies sensitively to a small change in the coating start timing. With this scheme, we have successfully fabricated a highly uniform OLED device with no dead zones in the emission area.

Recent research on anthracene-based hydrocarbon (PNA) as the emissive layer host found that deuteration mediated the formation of these adduct species, presumably quenchers, and thus improved the device lifetime. Meanwhile, studies on deuterium in PNA host materials with stepwise deuteration are scarce. In this work, we report a systematic study of isotopic effects through independent deuteration of the phenyl or/and the dibenzofuran unit on a series of PNA materials polyaromatic dibenzofuran (PAF, PAF-d₅, PAF-d₇ and PAF-d₁₂). We fabricated fluorescent OLED based on this triplet-triplet up-conversion active host materials for conventional MR-TADF emitter. A short-lived excited delayed lifetime of less than 2 μs has been observed in their electroluminescence decay studies. In addition, LT₈₀ of up to 12.7 h has been observed in PAF-d₁₂ at the brightness of 1000 cd m⁻², corresponding to a 4-fold enhancement of OLED stability compared to the non-deuterated counterpart. We hope the current research can provide insights for further device improvement.

In this work, three orthogonally bonded phenanthroimidazole based donor-acceptor (D-A) structured blue-emissive materials N-SBPMCN, N-ABPMCN and N-TBPMCN with different donor moieties are designed synthesized. Theoretical combined experimental researches proved that the involving of weak donor (spiro-fluorene and anthracene) and strong donor triphenylamine can form different locally-emissive (LE) dominated hybrid local and charge-transfer (HLCT) excited state, which can contribute to their high photoluminescent quantum yield (PLQY), satisfied electroluminescence performance and blue purity. Specifically, N-TBPMCN with strong donor triphenylamine that possesses more CT excited state components demonstrates the best electroluminescence performance and blue purity among the three materials, revealing that the molecular design of orthogonal D-A structure is of great potential in blue-emissive functional materials. Additionally, we also discovered that intermolecular CT state can also contribute to high exciton utilization.

Two electron-transport host materials are synthesized by linking anthracene with benzimidazole derivatives through a unit of methyl substituted phenyl. The methyl substitution generates a large dihedral angle between the benzimidazole plane and bridging phenyl, keeping the excited state distribution and energy levels of T₁ and S₁ unchanged. The electron-only devices reveal that the two hosts have obviously enhanced electron transport ability than that of Ph-AN-MBP without benzimidazole. As a result, the devices with Ph-AN-BIZ and N1-AN-BIZ as hosts and a blue multiple resonance material of tBuCz-DABNA as emitter exhibit high external quantum efficiency of 10.1 % and 9.1 %, respectively, and low turn-on voltage of 2.7 V, which is better than those of Ph-AN-MBP based device (7.9 %, 3.4 V). And their electroluminescence spectra have a very small full-width at half-maximum of 16.2 nm and pure blue color with CIE coordinates of (0.12, 0.11).

With the advent of numerous flexible optoelectronic applications, the importance of flexible and stable transparent conducting electrodes (TCEs) has been considerable. The conventional silver nanowire (AgNW) is a promising candidate as TCEs due to its decent opto-electrical properties and solution processibility. However, AgNW's high surface root mean square (RMS) roughness, relatively high sheet resistance, and low work function (∼4.5 eV) limit the usage for display applications. In this work, we design and study the AgNW and MXene (Ti₃C₂T_x) hybrid TCEs for flexible organic light-emitting diodes (OLEDs) to enhance the optoelectrical properties and the hole injection within the device. Experiment investigation is carried out via an application of AgNW/MXene (AgMX) hybrid TCEs as a bottom electrode for OLEDs devices in which the photolithography process and lift-off technique are employed for such fabrication. The hybrid TCEs indicate high optical transparency (86.8 % at 550 nm) and low sheet resistance (24.1 Ω/cm²) as well as improved surface morphology, enabling the efficient OLEDs operation. The optimized OLEDs exhibit a clear and stable red electroluminescence (EL) peak with an improved maximum external quantum efficiency (EQE) and luminance of 5.25 % and 3421.7 cd/m², respectively. Furthermore, the hybrid TCEs are readily formed on poly(ethylene terephthalate) (PET) substrate, showing high durability under the bending test up to 100,000 cycles. The results demonstrate that adopting AgMX TCEs is a reasonable strategy for obtaining proper flexible optoelectronic devices.

A method for preparing a single-layer encapsulation film using an organic-inorganic hybrid precursor solution processing was investigated. The film was created using a commodity epoxy and graphene oxide to ensure cost-effectiveness. Fast curing and annealing techniques, including microwave and intense pulsed light exposure, were employed. Calcium oxide nanoparticles were incorporated as a special moisture absorbent to improve the film's barrier properties. The barrier performance of the single layer encapsulation film was considerably enhanced by post-treatment of these nanoparticles. The characterization of the calcium oxide nanoparticles after post-treatment was performed using transmission electron microscopy with energy-dispersive X-ray spectroscopy, FT-IR, Brunauer-Emmett-Teller test. The composite epoxy encapsulation film, incorporating graphene oxide and post-treated calcium oxide nanoparticles, reduced water permeability approximately 400 times compared to the neat epoxy encapsulation film. This substantial improvement makes it suitable for use in flexible disposable electronics. The enhanced water vapor blocking efficiency is attributed to the combined effect of pathway block by graphene oxide and moisture absorption by calcium oxide.