Enhanced luminescence of a silica‐nitride phosphor; La3Si6N11:Ce3+by using Cr3+‐activated TiO2 nanoparticles

Author:

Aydin Ilkyaz1,Ertekin Kadriye234ORCID,Azem Funda Ak45,Delice Tulay Koc46,Birlik Isil45

Affiliation:

1. The Graduate School of Natural and Applied Sciences, Department of Chemistry Dokuz Eylul University Izmir Turkey

2. Center for Fabrication and Application of Electronic Materials Dokuz Eylul University Izmir Turkey

3. Department of Chemistry, Faculty of Science, Dokuz Eylul University 35390, Buca Izmir Turkey

4. Department of Nanoscience and Nano‐Engineering Dokuz Eylul University, The Graduate School of Natural and Applied Sciences Izmir Turkey

5. Department of Metallurgical and Materials Engineering Dokuz Eylul University Izmir Turkey

6. Türkiye Nuclear and Mineral Research Agency (TENMAK) Republic of Türkiye, Ministry of Energy and Natural Resources Ankara Turkey

Abstract

AbstractCe3+‐activated silica nitride phosphors (lanthanum silicate‐nitride [LSN]) are promising thermostable conversion components for white‐light‐emitting diodes, screen technologies, and other optoelectronic applications. Cr3+‐activated TiO2, on the other hand, is a strongly absorbing material depending on its size and optical microenvironment. In this work, we gathered Cr3+‐doped TiO2 and La3Si6N11:Ce3+ in an optically transparent polymethylmethacrylate matrix. Photoluminescence of the binary blends of La3Si6N11:Ce3+/TiO2 and La3Si6N11:Ce3+/TiO2:Cr3+ has been investigated under two different excitation energies by steady‐state and lifetime‐based measurements, respectively. When the microscale La3Si6N11:Ce3+ phosphor and nanoscale TiO2:Cr3+ particles were gathered at a critical concentration, the resulting composite exhibited 3.14‐fold enhancement in the emission signal intensity with respect to the additive‐free phosphor. Upon excitation, the La3Si6N11:Ce3+–TiO2:Cr3+ blend exhibited different excited‐state lifetimes for the nano‐ and microsecond time‐scales compared to the LSN. The microsecond time‐scale measurements performed under 378 nm excitation supported the existence of a potential energy transfer from the TiO2:Cr3+ to the La3Si6N11:Ce3+.

Publisher

Wiley

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