Self-heating in light-emitting electrochemical cells (LECs) has been long overlooked, while it has a significant impact on i) device chromaticity by changing the electroluminescent band shape, ii) device efficiency due to thermal quenching and exciton dissociation reducing the external quantum efficiency (EQE), and iii) device stability due to thermal quenching of excitons and formation of doped species, phase separation, and collapse of the intrinsic emitting zone. Herein, we reveal, for the first time, a direct relationship between self-heating and the early changes of the device chromaticity as well as the magnitude of the error comparing theoretical/experimental EQEs -i.e., overestimation error of ca. 35 % at usual pixel working temperatures of around 50 °C. This has been realized in LECs using a benchmark nanographene i.e., a substituted hexa-peri-hexabenzocoronene -as an emerging class of emitters with outstanding device performance compared to the prior-art of small molecule LECs -e.g., luminances of 345 cd/m 2 and EQEs of 0.35%. As such, this work is a fundamental contribution highlighting how self-heating is a critical limitation towards the optimization and wide use of LECs.