Okumura Ryosuke, Tanaka Hiroyuki, Shizu Katsuyuki, Fukushima Shohei, Yasuda Yuka, Kaji Hironori
Institute for Chemical Research, Kyoto University, Uji, Kyoto, 611-0011, Japan.
Angew Chem Int Ed Engl. 2024 Aug 26;63(35):e202409670. doi: 10.1002/anie.202409670. Epub 2024 Aug 13.
In thermally activated delayed fluorescence (TADF)-based organic light-emitting diodes (OLEDs), acceleration of reverse intersystem crossing (RISC) and suppression of intersystem crossing (ISC) are demanded to shorten a lifetime of triplet excitons. As a system realizing RISC faster than ISC, inverted singlet-triplet excited states (iST) with a negative energy difference (ΔE) between the lowest excited singlet and the lowest triplet states have been gathering much attention recently. Here, we have focused on an asymmetric hexa-azaphenalene (A6AP) core to obtain a new insight into iST. Based on A6AP, we have newly designed A6AP-Cz with the calculated ΔE of -44 meV. The experimental studies of a synthesized A6AP-Cz revealed that the lifetime of delayed fluorescence (τ) was only 54 ns, which was the shortest among all organic materials. The rate constant of RISC (k=1.9×10 s) was greater than that of ISC (k=1.0×10 s). The negative ΔE of A6AP-Cz was experimentally confirmed from 1) the k and k (-45 meV) and 2) the temperature-dependent τ. 3) The onsets of fluorescence and phosphorescence spectra at 77 K also supported the evidence of negative ΔE (-73 meV). This study demonstrated the potential of A6AP as an iST core for the first time.
在基于热激活延迟荧光(TADF)的有机发光二极管(OLED)中,需要加速反向系间窜越(RISC)并抑制系间窜越(ISC),以缩短三重态激子的寿命。作为一种实现RISC比ISC更快的体系,最低激发单重态和最低三重态之间具有负能差(ΔE)的反转单重态-三重态激发态(iST)最近备受关注。在此,我们聚焦于不对称六氮杂并苯(A6AP)核,以获得对iST的新见解。基于A6AP,我们新设计了A6AP-Cz,其计算得到的ΔE为 -44 meV。对合成的A6AP-Cz的实验研究表明,延迟荧光寿命(τ)仅为54 ns,这在所有有机材料中是最短的。RISC的速率常数(k = 1.9×10 s)大于ISC的速率常数(k = 1.0×10 s)。A6AP-Cz的负ΔE通过以下方式得到实验证实:1)k和k(-45 meV);2)与温度相关的τ。3)77 K下荧光和磷光光谱的起始点也支持了负ΔE(-73 meV)的证据。这项研究首次证明了A6AP作为iST核的潜力。