Abstract:Lead‐free halide perovskite nanocrystals (NCs) with the unique optical properties are of interest for broad applications. There are a few studies on near‐infrared (NIR) emission in perovskite NCs. Here, all‐inorganic rare‐earth‐based Cs2NaEr1−xBxCl6 (B: In, Sb, or Bi; x = 0, 0.13, and 0.5) double perovskite (DP) NCs have been successfully sythesized. The Cs2NaErCl6 NCs show good air stability and emit a sharp NIR photoluminescence (PL) at telecommunication wavelength of 1543 nm, originating from 4I13/2→4I15/2 … Show more
“…In addition, doping lanthanide ions in lead-free metal halide perovskite NCs is another effective strategy for achieving NIR emission. For instance, the doping of Yb 3+ can endow Cs 2 AgBiX 6 (X = Cl – or Br – ) and Cs 2 AgInCl 6 NCs with NIR emission around 980 nm, which is ascribed to the 2 F 5/2 → 2 F 7/2 transition of Yb 3+ ; , Cs 2 NaErCl 6 and Er 3+ -doped Cs 2 AgInCl 6 exhibit NIR emission centered at 1540 nm due to the 4 I 13/2 → 4 I 15/2 transition. , However, these previous efforts all focus on narrowband NIR emission, while the broadband NIR emitters with greater application potential such as in 3D sensing and food analyzing are rarely mentioned but are essential for the applications. Meanwhile, the tunability of the emission spectra that are equally important in NIR applications has not yet been achieved in such lead-free perovskite NCs.…”
Lead-free halide perovskite nanocrystals
(NCs) have attracted more
attention and demonstrated versatile potential in optoelectronic applications.
However, achieving broadband near-infrared (NIR) emission in such
materials remains a challenge. Herein, we successfully obtained Cr3+-doped Cs2AgInCl6 NCs via hot-injection
synthesis, which exhibits a NIR emission with a large full width at
half-maximum of 193 nm. Furthermore, tunable emission from 998 to
958 nm along with an enhanced photoluminescence quantum yield of 19.7%
is realized by gradually substituting Ag+ with Na+, and the blue shift luminescence behavior is attributed to a strengthened
crystal field around Cr3+. The excellent chemical and moisture
stability together with the as-fabricated Cs2NaInCl6:Cr3+ NC film made by screen printing showcases
its application potential in high-resolution images and NIR fluorescent
signs. This work proves the possibility of realizing tunable broadband
NIR emission in lead-free perovskite NCs and provides guidance for
expanding their application in the NIR region.
“…In addition, doping lanthanide ions in lead-free metal halide perovskite NCs is another effective strategy for achieving NIR emission. For instance, the doping of Yb 3+ can endow Cs 2 AgBiX 6 (X = Cl – or Br – ) and Cs 2 AgInCl 6 NCs with NIR emission around 980 nm, which is ascribed to the 2 F 5/2 → 2 F 7/2 transition of Yb 3+ ; , Cs 2 NaErCl 6 and Er 3+ -doped Cs 2 AgInCl 6 exhibit NIR emission centered at 1540 nm due to the 4 I 13/2 → 4 I 15/2 transition. , However, these previous efforts all focus on narrowband NIR emission, while the broadband NIR emitters with greater application potential such as in 3D sensing and food analyzing are rarely mentioned but are essential for the applications. Meanwhile, the tunability of the emission spectra that are equally important in NIR applications has not yet been achieved in such lead-free perovskite NCs.…”
Lead-free halide perovskite nanocrystals
(NCs) have attracted more
attention and demonstrated versatile potential in optoelectronic applications.
However, achieving broadband near-infrared (NIR) emission in such
materials remains a challenge. Herein, we successfully obtained Cr3+-doped Cs2AgInCl6 NCs via hot-injection
synthesis, which exhibits a NIR emission with a large full width at
half-maximum of 193 nm. Furthermore, tunable emission from 998 to
958 nm along with an enhanced photoluminescence quantum yield of 19.7%
is realized by gradually substituting Ag+ with Na+, and the blue shift luminescence behavior is attributed to a strengthened
crystal field around Cr3+. The excellent chemical and moisture
stability together with the as-fabricated Cs2NaInCl6:Cr3+ NC film made by screen printing showcases
its application potential in high-resolution images and NIR fluorescent
signs. This work proves the possibility of realizing tunable broadband
NIR emission in lead-free perovskite NCs and provides guidance for
expanding their application in the NIR region.
“…The long ms‐scale lifetime is attributed to Er 3+ forbidden 4 I 13/2 → 4 I 15/2 transitions. These preliminary results suggest Er 3+ ions are well‐incorporated inside the host lattice [ 13,18 ] and the existence of energy transfer from Mn 2+ to Er 3+ .…”
suitable penetration. [1] However, traditional NIR light sources, such as halogen lamps, tungsten lamps, suffer from several deficiencies, such as large sizes, low efficiency, short lifetimes, and poor matching degree with special infrared detectors, which provides the impetus to explore a new generation of high-performance NIR phosphor-converted lightemitting diodes (pc-LEDs) light sources. [2] In recent years, researchers have developed some lead halide perovskite materials with NIR photoluminescence (PL). [3] Although their excellent photoelectric properties, lead halide perovskites still face severe challenges which lack stability and the intrinsic toxicity of lead. [4] In order to solve these problems, we need to find stable, environmentally friendly metal halide perovskite materials with attractive optical properties.Recent studies have suggested an available option to substitute two divalent Pb 2+ ions with a pair of singly and triply charged cations in conventional lead halide perovskites while maintaining a 3D perovskite structure and charge neutrality to form the referred to double perovskites (DPs). [5] Among the possible DPs materials A
“…Recently, Miao and Han et al doped Er 3+ ions into the lead-free Cs 2 NaEr 1-x B x Cl 6 (B is In, Sb or Bi) perovskite NCs, thus, to obtain effective NIR emission at a telecommunication wavelength of 1543 nm. Such NIR emission can be mainly attributed to the energy transition from 4 I 13/2 → 4 I 15/2 to Er 3+ [ 74 ]. Recently, ultrasmall CsPbX 3 QDs formed on the surface of NaYF 4 :Yb/Tm@NaYF 4 :Yb core-shell UCNPs (see in Figure 6 e) and could exhibit tunable down-conversion PL and up-conversion PL under UV and NIR excitation, respectively, which can be potentially applied in the field of fluorescent anticounterfeiting technology [ 75 ].…”
Section: Application Of Ln
3+
In Perovskite Light-...mentioning
In recent years, rare-earth metals with triply oxidized state, lanthanide ions (Ln3+), have been demonstrated as dopants, which can efficiently improve the optical and electronic properties of metal halide perovskite materials. On the one hand, doping Ln3+ ions can convert near-infrared/ultraviolet light into visible light through the process of up-/down-conversion and then the absorption efficiency of solar spectrum by perovskite solar cells can be significantly increased, leading to high device power conversion efficiency. On the other hand, multi-color light emissions and white light emissions originated from perovskite nanocrystals can be realized via inserting Ln3+ ions into the perovskite crystal lattice, which functioned as quantum cutting. In addition, doping or co-doping Ln3+ ions in perovskite films or devices can effectively facilitate perovskite film growth, tailor the energy band alignment and passivate the defect states, resulting in improved charge carrier transport efficiency or reduced nonradiative recombination. Finally, Ln3+ ions have also been used in the fields of photodetectors and luminescent solar concentrators. These indicate the huge potential of rare-earth metals in improving the perovskite optoelectronic device performances.
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