Rapid synthesis and mechanochemical reactions of cesium copper halides for convenient chromaticity tuning and efficient white light emission
Lead halide perovskites are emerging as important candidates for many photoelectric applications; however, the toxicity of the heavy metal Pb poses a barrier to such applications. Thus, intense research efforts have been directed to developing lead-free photoelectric materials. Here, we report on th...
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Veröffentlicht in: | Journal of materials chemistry. C, Materials for optical and electronic devices Materials for optical and electronic devices, 2020-01, Vol.8 (14), p.4895-491 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Lead halide perovskites are emerging as important candidates for many photoelectric applications; however, the toxicity of the heavy metal Pb poses a barrier to such applications. Thus, intense research efforts have been directed to developing lead-free photoelectric materials. Here, we report on the synthesis and transformation of the cesium copper halides Cs
3
Cu
2
I
5
and CsCu
2
I
3
. These Cu based halide compounds are synthesized through a rapid antisolvent crystallization process with the use of isopropanol. The Cs
3
Cu
2
I
5
has blue emission at 445 nm with a full width at half maximum (FWHM) of ∼81.7 nm; CsCu
2
I
3
has a yellow emission at 575 nm with a FWHM of ∼119.9 nm. Notably, these two compounds can be interconverted through mechanochemical reactions. Therefore, standard white light emission can be obtained from a mixture of these two halides at an appropriate ratio and a white light emitting diode device is fabricated. We report a convenient route for rapid synthesis and easy tuning of Commission Internationale de l'Eclairage chromaticity coordinates to achieve white light emission. These findings might promote the large-scale synthesis of lead-free all-inorganic compounds for future applications in optoelectronic devices.
Emitting wavelength of cesium copper halides can be effectively tuned by regulating the process of mechanochemical reaction firstly. |
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ISSN: | 2050-7526 2050-7534 |
DOI: | 10.1039/d0tc00015a |