“…observed molecules gathering areas and reduction of built‐in potential at GBs in amplitude image of electrostatic force microscopy (EFM) ( Figure 3 a,b ) when adding a p‐type π ‐conjugated polymer poly[(2,6‐(4,8‐bis(5‐(2‐ethylhexyl) thiophen‐2‐yl)‐benzo[1,2‐ b :4,5‐ b ′] dithiophene))‐alt‐(5,5‐(1′,3′‐di‐2‐thienyl‐5′,7′‐bis(2‐ethylhexyl) benzo[1′,2′‐ c :4′,5′‐ c′ ] dithiophene‐4,8‐dione))] (PBDB‐T) in antisolvent. [ 27 ] The gathering of additives around perovskite GBs was similarly observed on other conjugated molecules such as fluorinated polymer PDTBDT‐FBT (Figure 3c ), poly[(9,9‐bis(3 0‐(( N , N ‐dimethyl)‐ N ‐ethyl‐ammonium)‐propyl)‐2,7‐fluorene)‐alt‐2,7‐(9,9‐dioctylfluorene)]di‐iodide (PFN‐I), [ 28 , 40 ] poly [(9,9‐bis(3′‐(( N , N ‐dimethyl)‐ N ‐ethylammonium)‐propyl)‐2,7‐fluorene)‐ alt ‐2,7‐(9,9‐dioctylfluorene)] dibromide (PFNBr), [ 80 ] triphenylphosphine oxides (TPPO), etc. [ 81 ] Moreover, it is found that the PeLEDs employing molecules with more phenyl groups show higher performance.…”