期刊
INORGANIC CHEMISTRY FRONTIERS
卷 6, 期 12, 页码 3621-3628出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c9qi00905a
关键词
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资金
- National Natural Science Foundation of China [51972020, 51832005, 51702329]
- Fundamental Research Funds for the Central Universities [FRF-TP-18-005A1]
- Beijing Natural Science Foundation [2182080]
Searching for high performance and broader applications of inorganic halide perovskites has drawn extensive attention. In this work, a Cr3+-doped halide perovskite, Cs2AgInCl6:Cr3+, which exhibits broadband near-infrared (NIR) emission is first obtained via the traditional high temperature solid-state reaction. A broad emission band ranging from 850 to 1350 nm centered at 1010 nm with a full-width at half-maximum (FWHM) of 180 nm is assigned to the spin-allowed T-4(2) -> (4)A(2) transition of octahedrally coordinated Cr3+ ions in a very weak crystal-field environment. The excitation bands centered at 353, 565 and 800 nm can be attributed to the absorption of the Cs2AgInCl6 host, the Cr3+ d-d transitions of (4)A(2) -> T-4(1) and (4)A(2) -> T-4(2), respectively. Upon 760 nm excitation, the photoluminescence quantum yield (PLQY) of Cs2AgIn0.9Cl6:0.1Cr(3+) is about similar to 22.03%. Cs2AgInCl6:Cr3+ phosphors with such broadband NIR emission have potential in phosphor converted light emitting diodes (pc-LEDs) which have applications in bioimaging and biomonitoring.
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