Luminescence Enhancement of Mn4+-Activated Fluorides via a Heterovalent Co-Doping Strategy for Monochromatic Multiplexing.
Yuanjing WangYayun ZhouHong MingYifei ZhaoEnhai SongQin-Yuan ZhangPublished in: ACS applied materials & interfaces (2021)
Mn4+ non-equivalent doped fluorides with high color purity red emission and relatively short decay time are crucial for wide color gamut displays and emerging applications, whereas the low quantum efficiency (QE) restrains their further applications. Herein, the luminescence of Mn4+ non-equivalent doped fluoride K2NaAlF6:Mn4+ (KNAF:Mn4+) is significantly enhanced via a heterovalent co-doping strategy, where the luminescence intensity is obviously increased by ∼85%, but the decay time is almost unchanged. The experimental characterization and density functional theory (DFT) calculations provide an understanding of the luminescence enhancement mechanism of heterovalent co-doping, which is enabled by simultaneously improving the stability of Mn4+ and reducing the number of quenching centers (defects and impurities). Combining the short-decay-time (τ = 4.03 ms) emission KNAF:Mn4+, Mg2+ and long-decay-time (τ = 9.23 ms) emission K2SiF6:Mn4+, a novel monochromatic multiplexing mode in the millisecond order is presented, which can be decoded not only in high-efficiency by a digital camera but also with a high security. This work provides a new optical multiplexing for the information security applications and also inspires the design of high-efficiency Mn4+-activated luminescent materials.
Keyphrases
- transition metal
- metal organic framework
- quantum dots
- density functional theory
- high efficiency
- room temperature
- energy transfer
- molecular dynamics
- ms ms
- multiple sclerosis
- high speed
- computed tomography
- magnetic resonance imaging
- machine learning
- magnetic resonance
- molecular dynamics simulations
- drinking water
- social media
- light emitting
- molecular docking
- highly efficient
- image quality