Highly sensitive permeation measurements are crucial for the characterization and development of polymeric substrates for flexible display applications. In particular, organic light-emitting devices require substrates with extremely low permeation rates for water and oxygen. Here we demonstrate a concept for measuring ultralow permeation rates. The amount of oxidative degradation in a thin Ca sensor is monitored by in situ resistance measurements. The benefits of this technique are demonstrated for polyester foils with single- and double-sided barrier coatings. A sensitivity limit is imposed by the quality of the encapsulation. The resulting base line contribution to the water vapor transmission rate of a glass reference is below 10−6 g/m2 day at accelerated test conditions.

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Due to their outstanding properties, e.g., good contrast, wide viewing angle, low power consumption, and self-emission organic light-emitting (OLE) displays on the basis of conjugated polymers are on the verge of commercialization. Two major disadvantages of the current processing technique for the polymers—spin coating—are the material waste and the difficulties involved in patterning multichrome or even full-color displays. Therefore, we investigated the screen-printing technique for the production of OLE displays. In this letter, we present performance data and images of screen-printed OLE diodes. They are already comparable to spin-coated ones. We observed luminance of 10 000 cd/m2 at 8 V and peak efficiencies exceeding 10 cd/A for green diodes. These data indicate that printed organic displays have the potential to replace “classical” spin-coated devices.

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Organic light-emitting diodes were fabricated on a 125-μm-thick polyethylene terephthalate substrate covered with 100 nm indium tin oxide. The luminance–current–voltage performance and the emission spectrum of the devices are investigated in the bent state under mechanical stress at different bending radii. Down to a curvature of 15 mm, no significant decrease in the device performance is found compared to the relaxed state, as well as to conventional devices on glass substrates.

Using a planar electrode geometry, the operational mechanism of iridium(III) ionic transition metal complex (iTMC)‐based light‐emitting electrochemical cells (LECs) is studied by a combination of fluorescence microscopy and scanning Kelvin probe microscopy (SKPM). Applying a bias to the LECs leads to the quenching of the photoluminescence (PL) in between the electrodes and to a sharp drop of the electrostatic potential in the middle of the device, far away from the contacts. The results shed light on the operational mechanism of iTMC‐LECs and demonstrate that these devices work essentially the same as LECs based on conjugated polymers do, i.e., according to an electrochemical doping mechanism. Moreover, with proceeding operation time the potential drop shifts towards the cathode coincident with the onset of light emission. During prolonged operation the emission zone and the potential drop both migrate towards the anode. This event is accompanied by a continuous quenching of the PL in two distinct regions separated by the emission line.