The d-f luminescence of Eu2+, Ce3+ and Yb2+ ions in Cs2MP2O7 (M = Ca2+, Sr2+)

17Citations
Citations of this article
31Readers
Mendeley users who have this article in their library.
Get full text

Abstract

The efficient narrow band emission of Eu2+ in Cs2MP2O7 (M = Ca2+, Sr2+) is characterized by a large Stokes shift and a high quenching temperature which makes the material promising for application in warm white LEDs. The unusual Eu2+ luminescence properties were reported recently but an explanation for the peculiar behavior is lacking. In this paper we aim at providing new insights in the luminescence of the Eu2+ emission in Cs2MP2O7 through measurements at cryogenic temperatures (down to 4 K) and by comparison with the d-f luminescence of Ce3+ and Yb2+ in the same host. The results reveal a sharp onset of the Eu2+ emission and excitation bands at 4 K. Usually the sharp onset for narrow excitation and emission bands coincide at an energy corresponding to the zero-phonon (purely electronic) transition, but for Eu2+ in Cs2MP2O7 there is a large shift of 3500 cm-1 between the onsets, consistent with the large Stokes shift observed. The onset shift can be explained by emission from a lower energy distorted excited 4f65d1 state. For Ce3+, the f-d absorption bands are at energies expected based on the relation between the absorption energies for Eu2+ and Ce3+ reported by Dorenbos. Contrary to Eu2+, the emission for Ce3+ shows a normal Stokes shift and therefore the emission bands are at much higher energies than predicted from the energy of the Eu2+ emission and the Dorenbos relations. Based on the present results the unusually large Stokes shift for the Eu2+ emission in Cs2MP2O7 is assigned to a Jahn-Teller like deformation in the excited 4f65d1 state of Eu2+ that is not present in the 5d state of Ce3+.

Cite

CITATION STYLE

APA

Senden, T., & Meijerink, A. (2016). The d-f luminescence of Eu2+, Ce3+ and Yb2+ ions in Cs2MP2O7 (M = Ca2+, Sr2+). Journal of Luminescence, 177, 254–260. https://doi.org/10.1016/j.jlumin.2016.04.050

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free