Spiro[fluorene-9,9′-xanthene]-based hole transporting materials modulated by mono- and bis- benzodioxino[2,3-b]pyrazine pendant groups for perovskite QLEDs.

In this work, we designed and synthesized two new hole-transporting materials with a nonplanar three-dimensional (3D) conformation. They were achieved by incorporating spiro[fluorene-9,9′-xanthene] as a cross-shaped configuration scaffold and adding either mono- (H1) or bis- benzodioxino[2,3-b]pyrazine (H2) pyrazine as pendant groups. Both compounds exhibit remarkable thermal stability, with thermal decomposition temperature (T d) of 462 (H1) and 504 °C (H2), respectively. Moreover, the structural substitution with benzodioxino[2,3-b]pyrazine units successfully aligned the energy levels of both materials with the perovskite quantum dot luminescence layer. Hereby, the fabricated perovskite QLEDs using H1 as hole-transporting materials (HTMs) featured an excellent average external quantum efficiency (EQE) of up to 9.5% with a maximum luminance of 22368 cd m−2, which is much higher than that of the H2 -based devices with an EQE of 6.6% under the same conditions. The excellent device performance from H1 can be attributed to its asymmetric structure by the introduction of monosubstituted benzodioxino[2,3-b]pyrazine groups, as evidenced by its high hole mobility of 1.90 × 10−4 cm2 V−1 s−1 and improved interface interaction with adjunct layers. Thus, this design approach may bring a fresh perspective to the utilization of solution-processable small-molecule HTMs in high-performance Pe-QLEDs and other optoelectronics in the future. [Display omitted] • Two spirofluorene-based hole transport materials with pyrazine were developed. • Both materials reveal excellent thermal stability, featuring high T g and T d. • They exhibit good hole transport capability and suitable energy level alignment. • Perovskite green QLEDs using single-pyrazine H1 achieved nearly 9.5% EQE avg. [ABSTRACT FROM AUTHOR]