Star-shaped carbazole derivative based efficient solid-state dye sensitized solar cell

International audienceTwo new star-shaped carbazole molecules, including tri(9-(methoxyphenyl)carbazol-3-yl)amine named TMPCA having molecular glasses properties and hole transport properties were synthesized. Their thermal, optical, photophysical and electrochemical properties were studied. The carbazole based molecules exhibit high thermal stability with 5% weight loss temperatures over 480 °C with higher glass temperature transitions 164-175 °C than the classical spiro-OMeTAD reference molecule. Their optical band gaps (2.76 eV) are low enough not to hinder neither the absorption of the indoline sensitizer (D102) nor its photoexcitation and charge transfer. Solid state ionization potential (IPs) of TMPCA is well adapted to that of D102 and ensure a driving force ΔrG >0.2 eV for an efficient transfer and regeneration of the photo-oxidized dye. Solid-state dye sensitized solar cells ITO/TiO2/D102/T4MPCA/Au showed a power conversion efficiency of 2.23% with Jsc of 8.85 mA cm−2 under standard AM 1.5 simulated solar irradiation

Three-terminal light-emitting device with adjustable emission color

A three-terminal organic light-emitting device with a periodic interrupted middle electrode is developed to allow for an adjustable emission color. The emission results from three independent light-emitting diodes with one diode utilizing exciplex emission. An equivalent electrical circuit is suggested taking the current–voltage characteristics and the direction of current flow through the organic structure into account. Two diodes are formed between the embedded middle electrode and the LiF/Al top and ITO bottom electrode, respectively, and the third diode utilizes that part of the device without the middle-electrode exhibiting exciplex emission. It will be shown that the spectrum of the emitted light can be tuned from blue to orange by controlling the applied potentials to the device terminals

Star-Shaped Carbazole Derivatives for Bilayer White Organic Light-Emitting Diodes Combining Emission from Both Excitons and Exciplexes

Star-shaped carbazole-based compounds were synthesized by the Buchwald–Hartvig method. The materials were examined by various experimental and theoretical methods, including differential scanning calorimetry, UV spectrometry, electron photoemission, time-of-flight techniques, and DFT (B3LYP) calculations. The synthesized compounds showed high thermal stability with the initial weight loss temperature higher than 400 °C. The electron photoemission spectra of the layers of the amorphous materials showed ionization potentials of 4.9 eV. Tri­(9-hexylcarbazol-3-yl)­amine showed high hole mobility (μ = 10^–3 cm² V^–1 s^–1 at an electric field of 3.6 × 10⁵ V/cm). The star-shaped compounds were used for the preparation of bilayer white organic light-emitting diodes which combine emission from both excitons and exciplexes. The brightness of the white organic light emitting diode at 7 V is 300 cd/m² with current efficiency 2.3 cd/A and CIE coordinates (0.37, 0.35) which are very close to the equienergy white point (0.33, 0.33)

Structure Properties Relationship of Donor–Acceptor Derivatives of Triphenylamine and 1,8-Naphthalimide

Solution-processable donor–acceptor molecules consisting of triphenylamine core and 1,8-naphthalimide arms were designed and synthesized by palladium-catalyzed Heck reaction. Dilute solutions of the synthesized compounds show strong absorption peaks in the visible wavelength range from 400 to 550 nm, which can be ascribed to the intramolecular charge transfer. Fluorescence quantum yields of dilute solutions of the synthesized materials range from 0.45 to 0.70, while those of the solid samples are in the range of 0.09–0.18. The synthesized molecules exhibit high thermal stability with the thermal degradation onset temperatures ranging from 431 to 448 °C. The compounds form glasses with glass-transition temperatures of 55–107 °C. DFT calculations show that HOMO and LUMO orbitals are almost entirely localized on the donor and acceptor moieties, respectively. Consequently, the frontier orbital energies for the three synthesized compounds are similar and practically do not depend on the number of 1,8-naphthalimide moieties. Ionization potentials of the solid samples (5.75–5.80 eV) are comparable. The charge-transporting properties of the synthesized materials were studied using xerographic time-of-flight method. Hole mobilities in the layers of the compounds having one and two 1,8-naphthalimide moieties exceed 10^–3 cm²·V^–1·s^–1 at high electric fields at room temperature. The differences on the hole mobilities between the three synthesized compounds are discussed in the frame of Marcus theory by comparing the reorganization energy and electronic coupling parameters