4.8 Article

First Synthesis of Mn-Doped Cesium Lead Bromide Perovskite Magic Sized Clusters at Room Temperature

期刊

JOURNAL OF PHYSICAL CHEMISTRY LETTERS
卷 11, 期 3, 页码 1162-1169

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpclett.9b03700

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资金

  1. NASA through MACES [NNX15AQ01A]
  2. NSF [CHE 1904547]
  3. NIH [R35GM131781]
  4. Fundamental Research Funds for the Central Universities [2018CDGFHG0012]
  5. UCSC Committee on Research Special Research Grant
  6. China Scholarship Council (CSC)
  7. National Natural Science Foundation of China (NSFC) [51702205]
  8. STU Scientific Research Foundation for Talents [NTF17001]
  9. Office of Science, Office of Basic Energy Sciences of the U.S. Department of Energy [DE-AC02-05CH11231]
  10. [JG2018103]
  11. [SKL-ACPS-C-03]

向作者/读者索取更多资源

Mn-doped CsPbBr3 perovskite magic sized clusters (PMSCs) are synthesized for the first time using benzoic acid and benzylamine as passivating ligands and MnCl2 center dot 4H(2)O 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 (similar to 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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