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Single Atom Silver‐Phosphors in Titanosilicate Matrix for Enhanced LED Applications.

Authors :
Romolini, Giacomo
Sun, Li
Fron, Eduard
Acapito, Francesco d'
Grandjean, Didier
Roeffaers, Maarten B.J.
Martìn, Cristina
Hofkens, Johan
Source :
Advanced Optical Materials. 3/22/2024, Vol. 12 Issue 9, p1-10. 10p.
Publication Year :
2024

Abstract

Small metal oligomers have gained significant attention due to their exceptional optoelectronic properties and versatile applications, ranging from sensors to imaging and catalysis. However, the need for matrices (silica, zeolites, or metal‐organic frameworks) to prevent aggregation into larger metallic particles reduces their potential applicability in light‐emitting devices (LEDs) due to their poor electrical properties. To address this issue, a novel semiconductor stabilizer, titanosilicate, is proposed as an innovative solution for Ag‐based luminescent materials. These results show that titanosilicate, characterized by high thermochemical stability and well‐defined semiconducting properties, is an ideal scaffold for Ag‐luminescent species. Optical spectroscopic techniques reveal that Ag‐titanosilicates feature an orange fluorescence with a photoluminescence quantum yield reaching 20%. In contrast, a combination of X‐ray diffraction, TEM, and XEOL‐X‐ray absorption spectroscopic techniques show that, unlike zeolites, the luminescent species consist of single Ag atoms. The electroluminescent properties of the proposed Ag‐titanosilicate are further investigated within a conventional LED architecture by using the new material as an emissive layer. The developed proof‐of‐concept LED exhibits a significant improvement of the ZEOLEDs, where a smaller low turn‐on voltage of 2 V (enabling energy‐efficient operation) and high color rendering index of 80 introduces exciting prospects for developing advanced Ag‐LED phosphors. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
21951071
Volume :
12
Issue :
9
Database :
Academic Search Index
Journal :
Advanced Optical Materials
Publication Type :
Academic Journal
Accession number :
176213106
Full Text :
https://doi.org/10.1002/adom.202301894