Zero-dimensional (0D) organic metal halide hybrids, in which organic and metal halide ions cocrystallize to form neutral species, are a promising platform for the development of multifunctional crystalline materials. Herein we report the design, synthesis, and characterization of a ternary 0D organic metal halide hybrid, (HMTA)₄ PbMn0.69 Sn0.31 Br₈ , in which the organic cation N-benzylhexamethylenetetrammonium (HMTA⁺ , C₁₃ H₁₉ N₄ ⁺ ) cocrystallizes with PbBr₄ ²⁻ , MnBr₄ ²⁻ , and SnBr₄ ²⁻ . The wide band gap of the organic cation and distinct optical characteristics of the three metal bromide anions enabled the single-crystalline "host-guest" system to exhibit emissions from multiple "guest" metal halide species simultaneously. The combination of these emissions led to near-perfect white emission with a photoluminescence quantum efficiency of around 73 %. Owing to distinct excitations of the three metal halide species, warm- to cool-white emissions could be generated by controlling the excitation wavelength.
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Xu et al. (2020) studied this question.
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