Abstract
High maximum external quantum efficiency (EQEmax ), small efficiency roll-offs, and long operational lifetime at practical luminances are three crucial parameters for commercialization of organic light-emitting diodes (OLEDs). To simultaneously achieve these goals, it is desirable to have the radiative decay rate constant (kr ) as large as possible, which, for a thermally activated delayed fluorescent (TADF) emitter, requires both a large S1 →S0 radiative decay rate constant (kr S ) and a small singlet-triplet energy gap (ΔEST ). Here, the design of a class of tetradentate gold(III) TADF complexes for narrowing the ΔEST while keeping the kr S large is reported. The as-synthesized complexes display green emission with close to unity emission quantum yields, and kr approaching 2× 106 s-1 in thin films. The vacuum-deposited green OLEDs based on 1 and 4 demonstrate maximum EQEs of up to 24 and 27% with efficiency roll-offs of 5.5 and 2.2% at 1000cd m-2 , respectively; the EQEs maintain high at 10000cd m-2 (19% (1) and 24% (4)). A long LT90 device lifetime of 1820h at 1000cd m-2 for complex 1 is achieved, which is one of the longest device lifetimes of TADF-OLEDs reported in the literature.
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