Abstract

Based on the strategy of using small cross-linkable thermally activated delayed fluorescence (TADF) molecules act as the host or the guest, a highly efficient TADF polymer is successfully constructed to develop efficient solution-processed organic light-emitting diodes (OLEDs). In this paper, two small cross-linkable TADF monomers, namely DV-2CzBN and DV-2CzTBN, are designed and synthesized. Simultaneously, small molecular TADF monomers are linked together using two vinylbenzyl linkers to form polymers. Systematic studies demonstrate that the polymers based on the host-guest TADF system can maintain the intrinsic TADF nature unchanged, and also effectively inhibit the triplet excitons quenching. Encouragingly a solution-processed OLED based on the host-guest system TADF polymer showed an excellent device performance with the maximum current efficiency (CE) of 25.1 cd A −1 , the power efficiency (PE) of 19.6 lm W −1 and external quantum efficiency (EQE) of 11.4%, respectively, which are two times higher in device efficiency than the corresponding device with the polymers based on the single-molecule system. Here, a new series of non-conjugated polymers were designed and synthesized based on the strategy of the host-guest system constructing with two small cross-linkable TADF molecules. • A new series of TADF polymers have been synthesized based on two small cross-linkable TADF molecules. • The TADF characteristics of small cross-linkable molecule are perfectly inherited by these VBN-based polymers. • The TADF behaviors can be improved by managing the content of DV-2CzTBN unit in the polymers. • The VBN10-based device can afford a high TADF OLED by solution process with EQE of 11.4%.

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