“…The evacuated samples were exposed to vapors from the precursors for approximately 10 min before purging excess precursor by evacuation. The precursors choices for the A-site cations were the same as one of the previous publications [17], bis(2,2,6,6-tetramethyl-3,5-heptanedionato) calcium (Ca(TMHD) 2 , Strem, Newburyport, MA, USA), bis(2,2,6,6-tetramethyl-3,5-heptanedionato) strontium hydrate (Sr(TMHD) 2 , Strem, USA), and bis(2,2,6,6-tetramethyl-3,5-heptanedionato) barium hydrate (Ba(TMHD) 2 , Strem, USA) were chosen for Ca, Sr, and Ba ALD processes, respectively, and the exposure was carried out at 573 K. Because the TMHD ligands can only be removed at elevated temperatures by air [26], the oxidation step of the ALD cycle for these precursors was performed by transferring the samples to a muffle furnace at 773 K for 5 min. For the TiO 2 -ALD process, Titanium chloride (TiCl 4 , Sigma-Aldrich, St. Louis, MO, USA) was chosen as the precursor.…”