Photocatalytic activity can be enhanced up to three times by confining the catalyst within a compact single-chain polymer nanoparticle environment, while retaining homocatalytic reaction conditions.
We introduce a ...
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The solid-state nanomorphology that enables aggregation-induced emission (AIE) is shown to be compatible with the ion redistribution that defines the operation of light-emitting electrochemical cells (LECs), and appropriately designed AIE-LECs are reported to deliver fast-to-turn and efficient emission at low voltage.
The emission efficiency of organic semiconductors (OSCs) often suffers from aggregation caused quenching (ACQ). An elegant solution is aggregation-induced emission (AIE), which constitutes the design of the OSC so that its morphology inhibits quenching π–π interactions and non-radiative motional deactivation. The light-emitting electrochemical cell (LEC) can be sustainably fabricated, but its function depends on motion of bulky ions in proximity of the OSC. It is therefore questionable whether the AIE morphology can be retained during LEC operation. Here, we synthesize two structurally similar OSCs, which are distinguished by that 1 features ACQ while 2 delivers AIE. Interestingly, we find that the AIE-LEC significantly outperforms the ACQ-LEC. We rationalize our finding by showing that the AIE morphology remains intact during LEC operation, and that it can feature appropriately sized free-volume voids for facile ion transport and suppressed non-radiative excitonic deactivation.Zum Volltext
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