Yan, Jie, Nakamura, Takeru, Tan, Xiaolan, Yiu, Shek-Man, Mimura, Ryunosuke, Hoshi, Keigo, Zhou, Xiuwen, Chi, Yun, Sasabe, Hisahiro, and Kido, Junji
[Display omitted] • Homoleptic Ir(III) emitters with electron deficient carbene cyclometalates. • High product selectivity in syntheses. • ∼100 % PLQY and fast radiative rate constant ∼106 s−1 in doped mCPCN thin film. • Achieving >30 % efficiency in the narrowband blue emissive hyper-OLED devices. Blue phosphors are indispensable in constructing organic light-emitting diodes (OLEDs). Herein, we reported two Ir(III) complexes, namely f -CN1 and f -CN2, with asymmetrically arranged benzo[d]imidazolylidenes, to which the peri -cyano substituent has concurrently induced both the selective aryl cyclometalation and emission tuning in giving one single blue Ir(III) phosphor. With the aforementioned 'one stone for two birds' tactics, these carbene complexes exhibited photoluminescent peak (λ max) at ∼472 nm and excellent quantum yields (83–100 %) in doped thin films. Consequently, the fabricated OLED devices delivered maximum external quantum efficiencies (EQE max) of 23.6 % and 20.2 %, respectively. Furthermore, hyper-OLED devices with f -CN1 and multi-resonant TADF terminal emitter m-DiNBO displayed an EQE max of 30.8 % with CIE x,y coordinates of (0.13, 0.10), together with impressive EQE of 26.9 % at practical brightness of 100 cd m−2. [ABSTRACT FROM AUTHOR]