Environmentally friendly, highly efficient, and large stokes shift-emitting ZnSe:Mn2+/ZnS core/shell quantum dots for luminescent solar concentrators
- Authors
- Byambasuren, Nyamsuren; Hong, A-Ra; Lee, Woo-Young; Byun, Ji Young; Kang, Gumin; Ko, Hyungduk; Jang, Ho Seong
- Issue Date
- 2022-10
- Publisher
- Nature Publishing Group
- Citation
- Scientific Reports, v.12, no.1
- Abstract
- In this study, heavy-metal-free orange light-emitting ZnSe:Mn2+/ZnS doped-core/shell (d-C/S) quantum dots (QDs) were synthesized using a nucleation doping strategy. To synthesize high quality d-C/S QDs with high photoluminescence (PL) quantum yield (QY), the Mn2+ concentration was optimized. The resulting ZnSe:Mn2+(5%)/ZnS d-C/S QDs showed a high PL QY of 83.3%. The optical properties of the synthesized QDs were characterized by absorption and PL spectroscopy. Their structural and compositional properties were studied by X-ray diffraction, transmission electron microscopy, and energy dispersive X-ray spectroscopy. After doping Mn2+ into a ZnSe core, the ZnSe:Mn2+/ZnS d-C/S QDs showed a large Stokes shift of 170 nm. The ZnSe:Mn2+/ZnS d-C/S QDs were embedded in a poly(lauryl methacrylate) (PLMA) polymer matrix and the ZnSe:Mn2+/ZnS-based polymer film was fabricated. The fabricated ZnSe:Mn2+/ZnS-PLMA film was highly transparent in the visible spectral region (transmittance > 83.8% for lambda >= 450 nm) and it exhibited bright orange light under air mass (AM) 1.5G illumination using a solar simulator. The optical path-dependent PL measurement of the ZnSe:Mn2+/ZnS-PLMA film showed no PL band shift and minimal PL decrease under variation of excitation position. These results indicate that the highly efficient and large Stokes shift-emitting ZnSe:Mn2+/ZnS QDs are promising for application to luminescent solar concentrators.
- Keywords
- MN-DOPED ZNSE; NANOCRYSTAL EMITTERS; OPTICAL-PROPERTIES; ENERGY; ABSORPTION; EMISSION; DYE
- ISSN
- 2045-2322
- URI
- https://pubs.kist.re.kr/handle/201004/114464
- DOI
- 10.1038/s41598-022-21090-x
- Appears in Collections:
- KIST Article > 2022
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