2023
DOI: 10.1016/j.orgel.2023.106816
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All organic transport materials (TMs) based QLEDs: Revisiting molecular electron TMs with mapping hole TMs via cross-linking strategy

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Cited by 2 publications
(5 citation statements)
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“…This cross-linking process was much more robust when comparing the fact that TFB:X1 and TFB:X2−X5 needed a weight ratio of 5:1 and 10:1, respectively. 26,39 Additionally, decreasing the weight ratio of X8/X9 to 50:1 can still maintain over 90% of the original absorbance after rinsing. These findings demonstrate the high solvent resistance of the two developed tridentate cross-linkers.…”
Section: Resultsmentioning
confidence: 99%
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“…This cross-linking process was much more robust when comparing the fact that TFB:X1 and TFB:X2−X5 needed a weight ratio of 5:1 and 10:1, respectively. 26,39 Additionally, decreasing the weight ratio of X8/X9 to 50:1 can still maintain over 90% of the original absorbance after rinsing. These findings demonstrate the high solvent resistance of the two developed tridentate cross-linkers.…”
Section: Resultsmentioning
confidence: 99%
“…By systematically optimizing the weight ratios of TFB:X8/X9, it was found that the tridentate carbene precursors, X8 and X9, both can provide cross-linked films with >95% solvent resistance even at an extremely low cross-linker weight ratio of 30:1 (TFB:X8/X9). This cross-linking process was much more robust when comparing the fact that TFB:X1 and TFB:X2–X5 needed a weight ratio of 5:1 and 10:1, respectively. , Additionally, decreasing the weight ratio of X8/X9 to 50:1 can still maintain over 90% of the original absorbance after rinsing. These findings demonstrate the high solvent resistance of the two developed tridentate cross-linkers.…”
Section: Resultsmentioning
confidence: 99%
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“…The TFB is one of the most widely used HTLs in QLEDs due to the high hole carrier mobility; however, its highest occupied molecular orbital (HOMO) is about −5.3 ± 0.1 eV, which is not suitable for the QD with deep energy bands, especially the green and blue QDs . Various chemical approaches were reported to modify the molecular structure of TFB to lower the HOMO toward better energy-level alignments. , For example, a TFB derivative with 2-cyanopropan-2-yl was developed with high conductivity and stabilized HOMO for the QLED applications . TF-DCF3 was also developed with two electron-withdrawing trifluoromethyl groups attached to the triphenylamine units, leading to 0.22 and 0.07 eV downshifts of the E HOMO and the lowest unoccupied molecular orbital energy level ( E LUMO ), respectively, agreeing with the previous report .…”
Section: Resultsmentioning
confidence: 99%