光致发光
掺杂剂
材料科学
钙钛矿(结构)
兴奋剂
钝化
量子点
激子
分析化学(期刊)
纳米技术
化学
光电子学
结晶学
凝聚态物理
物理
色谱法
图层(电子)
作者
Ke Xu,Evan T. Vickers,Binbin Luo,A’Lester C. Allen,Eefei Chen,Graham Roseman,Qihui Wang,David S. Kliger,Glenn L. Millhauser,Wen Yang,Xueming Li,Jin Z. Zhang
标识
DOI:10.1021/acs.jpclett.9b03700
摘要
Mn-doped CsPbBr3 perovskite magic sized clusters (PMSCs) are synthesized for the first time using benzoic acid and benzylamine as passivating ligands and MnCl2·4H2O and MnBr2 as the Mn2+ dopant sources at room temperature. The same approach is used to prepare Mn-doped CsPbBr3 perovskite quantum dots (PQDs). The concentration of MnX2 (X = Cl or Br) affects the excitonic absorption of the PMSCs and PQDs. A higher concentration of MnX2 favors PMSCs over PQDs as well as higher photoluminescence (PL) quantum yields (QYs) and PL stability. The large ratio between the characteristic Mn emission (∼590 nm) and the host band-edge emission shows efficient energy transfer from the host exciton to the Mn2+ dopant. PL excitation, electron paramagnetic resonance, and time-resolved PL results all support Mn2+ doping in CsPbBr3, which likely replaces Pb2+ ions. This study establishes a new method for synthesizing Mn-doped PMSCs with good PL stability, high PLQY and highly effective passivation.
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