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.
Following a simple thermodynamic model, which predicts that an array of non-wettable pores can be filled by dewetting of sufficiently thin films, we use molecular dynamics to simulate the rupture of nanometre-thick liquid Au films on nanoporous substrates. Our simulations clearly exhibit spinodal dewetting and hole nucleation, and some of the metal is indeed absorbed by non-wettable pores solely as a virtue of the Laplace pressure acting on dewetted droplets and rivulet-like structures. Finally, we show that the fraction of absorbed Au can be increased through patterning of the initial film.
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