Gutiérrez Mario, de la Hoz Tomás Mario, Rakshit Soumyadipta, Lezama Luis, Cohen Boiko, Douhal Abderrazzak
Departamento de Química Física, Facultad de Ciencias Ambientales y Bioquímica, e INAMOL, Campus Tecnológico de Toledo, Universidad de Castilla-La Mancha (UCLM), Avenida Carlos III, S.N., Toledo, 45071, Spain.
Departamento de Química Orgánica e Inorgánica, Facultad de Ciencia y Tecnología, Universidad del País Vasco, UPV/EHU, B° Sarriena s/n, Leioa, 48940, Spain.
Adv Sci (Weinh). 2024 Jul;11(26):e2400879. doi: 10.1002/advs.202400879. Epub 2024 Apr 24.
Luminescent Mn(II)-based organic-inorganic hybrid halides have drawn attention as potential materials for sensing and photonics applications. Here, the synthesis and characterization of methylammonium (MA) manganese bromide ((MA)BrMn(HO), (n = 1, 4 and x = 3, 6)) with different stoichiometries of the organic cation and inorganic counterpart, are reported. While the Mn centers have an octahedral conformation, the two coordinating water molecules are found either in cis (1) or in trans (2) positions. The photophysical behavior of 1 reflects the luminescence of Mn in an octahedral environment. Although Mn in 2 also has octahedral coordination, at room temperature dual emission bands at ≈530 and ≈660 nm are observed, explained in terms of emission from Mn in tetragonally compressed octahedra and self-trapped excitons (STEs), respectively. Above the room temperature, 2 shows quasi-tetrahedral behavior with intense green emission, while at temperatures below 140 K, another STE band emerges at 570 nm. Time-resolved experiments (77-360 K) provide a clear picture of the excited dynamics. 2 shows rising components due to STEs formation equilibrated at room temperature with their precursors. Finally, the potential of these materials for the fabrication of color-tunable down-converted light-emitting diode (LED) and for detecting polar solvent vapors is shown.
基于发光锰(II)的有机-无机杂化卤化物作为传感和光子学应用的潜在材料受到了关注。本文报道了具有不同化学计量比的有机阳离子和无机对应物的甲基铵(MA)溴化锰((MA)BrMn(HO),(n = 1, 4且x = 3, 6))的合成与表征。虽然锰中心具有八面体构象,但两个配位水分子处于顺式(1)或反式(2)位置。1的光物理行为反映了八面体环境中锰的发光。尽管2中的锰也具有八面体配位,但在室温下观察到≈530和≈660 nm处的双发射带,分别解释为来自四方压缩八面体中的锰和自陷激子(STE)的发射。在室温以上,2表现出具有强烈绿色发射的准四面体行为,而在低于140 K的温度下,另一个STE带在570 nm处出现。时间分辨实验(77 - 360 K)提供了激发动力学的清晰图像。2显示出由于STE形成而产生的上升成分,在室温下与其前体达到平衡。最后,展示了这些材料用于制造颜色可调下转换发光二极管(LED)以及检测极性溶剂蒸气的潜力。