Band Gap Tuning in Mercaptoacetic Acid Capped Mixed Halides Perovskites and Effect of Solvents on Their Fluorescence Dynamics: A Potential Sensor for Polarity.

From synthesis to application, there are always certain interactions between the polar solvents and perovskite nanocrystals (NCs). To explain the effect of solvent polarity especially on the photoluminescence (PL) properties of NCs is highly desirable, especially for sensing applications. Herein We have synthesized the methylammonium lead mixed halides (MAPbClBr, where n = 0, 0.5, 1, 1.5) perovskite nanocrystals (NCs) at room temperature by using ligand-assisted re-precipitation (LARP) method, by employing mercaptoacetic acid (MAA) as a capping ligand. Different techniques have been employed to get information regarding the structural and optical properties of the synthesized material. Powder X-ray diffraction (PXRD) confirms the orthorhombic crystal structure of the MAPbClBr perovskite NCs. FT-IR (Fourier-transform infrared) analysis confirms the successful interaction of capping ligands with NCs. By increasing MABr precursor concentration during the synthesis of perovskite NCs, a red shift in the UV-Vis absorption and PL spectra has been observed. The steady-state photoluminescence (SSPL) and time-resolved photoluminescence (TRPL) techniques suggested that these perovskite NCs exhibit tunable PL relative to the substitution of Cl with Br in NCs. The comparative PL studies in non-polar (benzene) and polar (tetrahydrofuran (THF)) revealed that the PL properties are highly sensitive and selective toward the solvent chosen. All synthesized NCs possess longer PL lifetime in benzene than in THF. Relatively, perovskite NCs synthesized with 0.166 mM MABr precursor concentration show a longer PL lifetime (6.51 ns in benzene) as compared to other MABr concentrations. These studies not only propose that by controlling precursors concentration, one can synthesize NCs having tunable PL with a longer radiative PL lifetime, but also provide a comparative understanding of PL dynamics of NCs in different solvents.