有机化学 ›› 2025, Vol. 45 ›› Issue (11): 4202-4209.DOI: 10.6023/cjoc202503027 上一篇    下一篇

研究论文

基于分子内电荷转移技术构建高效热激活延迟荧光型有机余辉材料

罗婷a,b, 肖宇峰b, 李珣b, 夏雯a,b, 张卡卡a,b,*()   

  1. a 四川师范大学化学与材料科学学院 成都 610066
    b 中国科学院上海有机化学研究所 金属有机化学全国重点实验室 金属有机化学全国重点实验室 上海 200032
  • 收稿日期:2025-03-26 修回日期:2025-04-27 发布日期:2025-06-11
  • 基金资助:
    国家自然科学基金(22475228); 国家自然科学基金(22175194)

Fabrication of Highly-Efficient Thermally Activated Delayed Fluorescence-Type Organic Afterglow Materials Based on Intramolecular Charge Transfer Technology

Ting Luoa,b, Yufeng Xiaob, Xun Lib, Wen Xiaa,b, Kaka Zhanga,b,*()   

  1. a College of Chemistry and Materials Science, Sichuan Normal University, Chengdu 610066
    b State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032
  • Received:2025-03-26 Revised:2025-04-27 Published:2025-06-11
  • Contact: *E-mail: zhangkaka@sioc.ac.cn
  • Supported by:
    National Natural Science Foundation of China(22475228); National Natural Science Foundation of China(22175194)

报道了基于热激活延迟荧光(TADF)机制的高效可见光激发余辉材料的构筑, 采用分子内电荷转移技术, 所得的TADF型余辉材料展示了数百毫秒的发射寿命和50%左右的光致发光量子产率, 表现出显著的温度响应特性. 通过在给体-受体(D-A)型二氟化硼β-二酮(BF2bdk)分子中引入额外的电子供体基团, 设计了给体-受体-给体(D-A-D)型化合物, 所得化合物表现出适度的反向系间窜越速率, 促进了BF2bdk在刚性晶体基质中的TADF型余辉的出现. 此外, D-A-D设计方法提高了最高占据分子轨道能级, 从而实现了在可见光激发下的TADF型余辉发射. 研究结果表明分子内电荷转移技术在推进高性能有机TADF型余辉材料设计中的重要性.

关键词: 二氟化硼β-二酮, 热激活延迟荧光, 有机余辉, 室温磷光, 分子内电荷转移

The construction of highly efficient visible-light-excitable afterglow materials based on thermally activated delayed fluorescence (TADF) mechanism is reported, employing an intramolecular charge transfer technology. The resulting TADF- type afterglow materials exhibit emission lifetimes in the range of hundreds of milliseconds and photoluminescence quantum yields of approximately 50%, demonstrating remarkable temperature-responsive properties. By introducing additional electron- donating groups into the donor-acceptor (D-A)-type difluoroboron β-diketonate (BF2bdk) molecules, donor-acceptor-donor (D-A-D)-type compounds were designed. These compounds exhibit a moderate rate of reverse intersystem crossing (RISC), thereby promoting the emergence of TADF-type afterglow within a rigid crystalline matrix. Furthermore, the D-A-D design approach elevates the highest occupied molecular orbital (HOMO) energy level, enabling TADF-type afterglow emission under visible light excitation. The research findings highlight the significance of intramolecular charge transfer technology in advancing the design of high-performance organic TADF-type afterglow materials.

Key words: difluoroboron β-diketonate, thermally activated delayed fluorescence, organic afterglow, room-temperature phos- phorescence, intramolecular charge transfer