Issue 12, 2016

A novel double-perovskite Gd2ZnTiO6:Mn4+ red phosphor for UV-based w-LEDs: structure and luminescence properties

Abstract

Red-emitting Mn4+ activated oxide phosphors with a cheap price and excellent physical/chemical stability have become a hot research topic for their potential applications in white LEDs (w-LEDs). Herein, we report a novel double-perovskite Gd2ZnTiO6:Mn4+ (GZT:Mn4+) red phosphor. The material microstructures were characterized with the aid of XRD Rietveld refinement and HRTEM observations. The luminescence properties and dynamics of Mn4+ in GZT were studied in detail using low/room temperature steady/transient spectroscopic techniques. The crystal field strength and nephelauxetic effect influencing the Mn4+ emission energy were also analyzed. It is revealed that the special crystal structure of GZT featuring alternately slant-wise arranged [TiO6]/[ZnO6] octahedrons with the [–Mn4+–O2−–Zn2+–] bond angle deviating from 180° is beneficial to achieving efficient Mn4+: 2Eg4A2 transition in the deep-red region. After mixing the red-emitting GZT:Mn4+ with the commercial blue and green phosphors in various ratios, and then coupling the mixture with a 365 nm UV chip to build a w-LED, the white light was found to evolve from cool to warm with a tunable correlated color temperature (CCT) from 6977 K to 4742 K, a color rendering index (CRI) up to 82.9, and an improved R9 value to 43, which validates that GZT:Mn4+ is a promising red color converter for UV-based w-LEDs.

Graphical abstract: A novel double-perovskite Gd2ZnTiO6:Mn4+ red phosphor for UV-based w-LEDs: structure and luminescence properties

Supplementary files

Article information

Article type
Paper
Submitted
22 Jan 2016
Accepted
29 Feb 2016
First published
01 Mar 2016

J. Mater. Chem. C, 2016,4, 2374-2381

A novel double-perovskite Gd2ZnTiO6:Mn4+ red phosphor for UV-based w-LEDs: structure and luminescence properties

H. Chen, H. Lin, Q. Huang, F. Huang, J. Xu, B. Wang, Z. Lin, J. Zhou and Y. Wang, J. Mater. Chem. C, 2016, 4, 2374 DOI: 10.1039/C6TC00313C

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