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  • Mechanism for Broadband White-Light Emission from Two-Dimensional (110) Hybrid Perovskites JOURNAL OF PHYSICAL CHEMISTRY LETTERS Hu, T., Smith, M. D., Dohner, E. R., Sher, M., Wu, X., Tuan Trinh, M., Fisher, A., Corbett, J., Zhu, X., Karunadasa, H. I., Lindenberg, A. M. 2016; 7 (12): 2258-2263

    Abstract

    The recently discovered phenomenon of broadband white-light emission at room temperature in the (110) two-dimensional organic-inorganic perovskite (N-MEDA)[PbBr4] (N-MEDA = N(1)-methylethane-1,2-diammonium) is promising for applications in solid-state lighting. However, the spectral broadening mechanism and, in particular, the processes and dynamics associated with the emissive species are still unclear. Herein, we apply a suite of ultrafast spectroscopic probes to measure the primary events directly following photoexcitation, which allows us to resolve the evolution of light-induced emissive states associated with white-light emission at femtosecond resolution. Terahertz spectra show fast free carrier trapping and transient absorption spectra show the formation of self-trapped excitons on femtosecond time-scales. Emission-wavelength-dependent dynamics of the self-trapped exciton luminescence are observed, indicative of an energy distribution of photogenerated emissive states in the perovskite. Our results are consistent with photogenerated carriers self-trapped in a deformable lattice due to strong electron-phonon coupling, where permanent lattice defects and correlated self-trapped states lend further inhomogeneity to the excited-state potential energy surface.

    View details for DOI 10.1021/acs.jpclett.6b00793

    View details for Web of Science ID 000378196000017

    View details for PubMedID 27246299