ABSTRACT
Conjugated polymers featuring thermally activated delayed fluorescence (TADF) attract tremendous attention in both academic and industry communities due to their easy solution processing for fabricating large-area and low-cost high-performance polymer light-emitting diodes (PLEDs). However, current nondoped solution-processed PLEDs frequently encounter significant efficiency roll-offs and unreasonably high operating voltages at high brightness, especially for red-emitting polymers. Herein, we design hyperbranched conjugated polymers (HCPs) with D-A-D type TADF characteristics for high-performance red-emitting PLEDs. Multiple intramolecular charge transfer (ICT) channels induced by quasi-equivalent donors of the TADF core strongly boost the reverse intersystem crossing (RISC) process and singlet excitons radiative transition. Coupling with the efficient energy transfer process generated by structure advantages of HCPs, the strongly electron-withdrawing oxygen atoms located on the TADF cores further accelerate hole transportation from the host chains to the TADF cores. Under a rational regulation of the TADF core ratio, the related nondoped red-emitting device performs an outstanding performance with an EQEmax of 8.39% and exhibits no roll-off while the luminance is less than 100 cd/m2 and only 3.3% decrease at 500 cd/m2. Simultaneously, the EQE can maintain 7.4% under 1000 cd/m2. Furthermore, the corresponding nondoped device exhibits a low turn-on voltage of around 2.5 V and achieves a luminance of 500 cd/m2 at 3.5 V and even 1000 cd/m2 at 3.9 V. To our knowledge, this is the best performance among all nondoped red PLEDs with high brightness obtained at low operating voltage.
ABSTRACT
The blends of high and low molecular weights poly(ε-caprolactone) (PCL) with poly(vinyl chloride (PVC) were prepared. The samples before and after the crystallization of PCL were uniaxially stretched to different draw ratios. The orientation features of PCL in a stretched crystalline PCL/PVC blend and crystallized from the amorphous PCL/PVC blends under varied strains were studied by wide-angle X-ray diffraction (WAXD) diffraction. It was found that a uniaxial stretching of crystalline PCL/PVC blend with high molecular weight PCL results in the c-axis orientation along the stretching direction, as is usually done for the PCL bulk sample. For the stretched amorphous PCL/PVC blend samples, the crystallization of high molecular weight PCL in the blends under a draw ratio of λ = 3 with a strain rate of 6 mm/min leads to a ring-fiber orientation. In the samples with draw ratios of λ = 4 and 5, the uniaxial orientation of a-, b-, and c-axes along the strain direction coexist after crystallization of high molecular weight PCL. With a draw ratio of λ = 6, mainly the b-axis orientation of high molecular weight PCL is identified. For the low molecular weight PCL, on the contrary, the ring-fiber and a-axis orientations coexist under a draw ratio of λ = 3. The a-axis orientation decreases with the increase of draw ratio. When the λ reaches 5, only a poorly oriented ring-fiber pattern has been recognized. These results are different from the similar samples stretched at a higher strain rate as reported in the literatures and demonstrate the important role of strain rate on the crystallization behavior of PCL in its blend with PVC under strain.
