In this letter, we investigate electronic structures and electron-injection mechanisms of the effective cathode structures for organic light-emitting devices incorporating cesium carbonate ͑Cs 2 CO 3 ͒, either deposited as an individual thin injection layer or doped into the organic electron-transport layers. The electronic structures and the interface chemistry studied by ultraviolet and x-ray photoemission spectroscopy show that the enhanced electron injection is associated with strong n-doping effects and increase of electron concentrations in the electron-transport layer induced by Cs 2 CO 3. Since such a reaction occurs without the presence of metals, cathode structures incorporating Cs 2 CO 3 may be applied to a wide range of electrode materials.

A new dye, SSD1, featuring two donor/acceptor chromophores aligned in a spiro configuration with two anchoring groups separated at a distance of 10.05 A (closely matching the distance between the adsorption sites of the anatase TiO(2) surface) undergoes efficient dye adherence on TiO(2) films. A dye-sensitized solar cell incorporating SSD1 exhibited a short-circuit current of 8.9 mA cm(-2), an open-circuit voltage of 0.63 V, a fill factor of 0.67, and a power conversion efficiency of 3.75%.

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A novel ambipolar spiro-configured D-A blue-light emitter bearing hole-transporting diphenylamino groups and electron-transporting phenylbenzimidazole groups was synthesized, characterized, and incorporated into an efficient single-layer organic light-emitting diode (OLED) device exhibiting blue-emission Commission International d'Eclairage (CIE) coordinates of 0.15 and 0.14, a turn-on potential of 4 V, a maximum brightness of 2800 cd/m2 at 830 mA/cm2 (19 V), and a maximum quantum efficiency of 0.53% (0.61 cd/A).