摘要
The rapid development of organic-inorganic metal halides in optoelectronic devices has been considered a promising approach for light-emitting diodes. Mn-based halogen hybrids represent a class of fascinating luminescence functional materials . Up to date, studies on Mn-based metal halides remain blurry and suffer from instability and low photoluminescence quantum yield (PL QY). Here, the single crystalline of MEA(MnBr 4- x Cl x ) 2 (MEA=((CH 3 ) 4 N)((C 2 H 5 ) 4 N) 2 ·NH 4 , x = 0, 2, 3) were designed and constructed by a one-pot solution method for the first time, featuring brilliant green emissions under ultraviolet light and revealing PL QY up to 99 ± 1% with x = 3 at room temperature. The excellent luminescence is ascribed to the Mn 2+ d 5 configuration with the 4 T 1 – 6 A 1 transition. Moreover, the thermostability and anomalous photoluminescence (PL) behavior triggered by heat are modulated via varying halogen ratio Cl/Br. Particularly, MEA(MnBr 4 ) 2 has an ultrahigh melting up to 600 K, which is, as we know, the highest one among the Mn-based organic-inorganic hybrid compounds. Our findings not only present the outstanding performance of three crystals, but also highlight the potential of these compounds in optoelectronics.
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