Solid-state light-emitting electrochemical cells (LECs) using sustainable and eco-friendly materials and affording high brightness, efficiency, and stability are highly desired. Here, intrinsically ionic, thermally activated delayed fluorescence (TADF) materials 1-3 for efficient, bright, and stable LECs are reported. 1-3 feature carbazole-type donors and cationic triazine-type acceptors, which are located ortho to each other on the phenyl linkers. Through-space chargetransfer (CT) dominates the CT transitions in 1-3. In doped and neat films, 1-3 show blue and green TADF emission, respectively, with reverse intersystem crossing rates at around 7.0 × 10 5 s −1 . 1-3 possess excellent electrochemical stability (except for the oxidation of 1) and film-forming abilities. LECs using neat films of 1-3 as the single active layers afford green electroluminescence with peak brightness/peak external quantum efficiency (EQE) of up to 572 cd m −2 /6.8% under 4.0 V and peak brightness/peak EQE/halflifetime of up to 860 cd m −2 /5.4%/48 h under 50 A m −2 . A longer half-lifetime of 218 h has further been achieved at 162 cd m −2 under 10 A m −2 . The work reveals the bright prospect for the development of efficient, bright, and stable LECs with intrinsically-ionic TADF materials.