Journal
NANO RESEARCH
Volume 15, Issue 7, Pages 6422-6429Publisher
TSINGHUA UNIV PRESS
DOI: 10.1007/s12274-022-4277-7
Keywords
bismuth; luminescent nanocrystals; metal halide; excited-state dynamics; electron-phonon coupling
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Funding
- National Natural Science Foundation of China (NSFC) [12074379, U1805252, 21875250, 12074380, 11904365, 12004384]
- Chinese Academy of Sciences/State Administration of Foreign Experts Affairs (CAS/SAFEA) International Partnership Program for Creative Research Teams
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This study reports a controlled synthesis strategy for Bi3+-doped Cs2SnCl6 nanocrystals and investigates the excited-state dynamics of Bi3+ through spectroscopic methods, revealing the origin and characteristics of its photoluminescence.
Luminescent metal halides doped with ns(2)-metal ions such as 6s(2)-metal Bi3+ have aroused reviving interest owing to their outstanding optical properties; however, the origin of the photoluminescence (PL) remains controversial and unclear. Herein, we report a strategy for the controlled synthesis of Bi3+-doped vacancy-ordered double perovskite Cs2SnCl6 nanocrystals (NCs) and unravel the triplet excited-state dynamics of Bi3+ through temperature-dependent PL and ultrafast femtosecond transient absorption spectroscopies. Owing to the aliovalent Bi3+ doping in the spatially confined zero-dimensional (OD) structure of Cs2SnCl6, Bi3+ ions experience an enhancive Jahn-Teller distortion in the excited state, which results in intense broadband blue PL originating from the inter-configurational P-3(0,1) -> S-1(0) transitions of Bi3+ at 450 nm, with a large Stokes shift and a quantum yield of 35.2%. Specifically, an unusual thermal-enhanced Jahn-Teller splitting of the excitation band and a remarkable transition of the PL lifetime from ms at 10 K to mu s at 300 K were observed, as solid evidence for the isolated Bi3+ emission. These findings clarify the controversy about the PL origin in ns(2)-metal ion-doped lead-free luminescent metal halides, thereby paving the way for exploring their optoelectronic applications.
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