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Molecular engineering towards efficientwhite-light-emitting perovskite.

ABSTRACT: Low-dimensional hybrid perovskites have demonstrated excellent performance as white-light emitters. The broadband white emission originates from self-trapped excitons (STEs). Since the mechanism of STEs formation in perovskites is still not clear, preparing new low-dimensional white perovskites relies mostly on screening lots of intercalated organic molecules rather than rational design. Here, we report an atom-substituting strategy to trigger STEs formation in layered perovskites. Halogen-substituted phenyl molecules are applied to synthesize perovskite crystals. The halogen-substituents will withdraw electrons from the branched chain (-R-NH₃⁺) of the phenyl molecule. This will result in positive charge accumulation on -R-NH₃⁺, and thus stronger Coulomb force of bond (-R-NH₃⁺)-(PbBr₄^2-), which facilitates excitons self-trapping. Our designed white perovskites exhibit photoluminescence quantum yield of 32%, color-rendering index of near 90 and chromaticity coordinates close to standard white-light. Our joint experiment-theory study provides insights into the STEs formation in perovskites and will benefit tailoring white perovskites with boosting performance.

SUBMITTER: Zhang M

PROVIDER: S-EPMC8361204 | biostudies-literature |

REPOSITORIES: biostudies-literature

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