Two Photon NIR-to-Red Upconversion Mechanism in CaF 2 :Er 3+ , Yb 3+

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Authors: Zhifeng Deng, Hao Wu, Hao Wu, Huajun Wu, Huajun Wu, Yongshi Luo, Liangliang Zhang, Zhendong Hao, Feng Liu, X. Wang, Jiahua Zhang
Cited by: 5
References: 37

Abstract

The popular Er 3+ –Yb 3+ upconversion (UC) system generates green and red emissions under near-infrared (NIR) 980 nm excitation. The green emission is a two-photon process, whereas for the red emission two and three photon process are both possible, depending on host. Fluoride hosts generally favor a three-photon process because fluorides have low phonon energies and multiphonon relaxation (MPR) involved in the usual two-photon process is suppressed. However, CaF 2:Er 3+ /Yb 3+ exceptionally produces an intense two-photon upconverted red emission. Here, we show that the red UC emission in CaF 2 is generated mainly by an unusual two-photon UC mechanism that enables efficient relaxation from the UC pumped green emitting state to the red emitting state via round trip energy transfer (RTET) between Er 3+ and Yb 3+ . The efficient RTET in CaF 2 is attributed to the unique characteristic of CaF 2 in which rare earth ions are prone to clustering. The contribution of RTET to red UC emission is evaluated for various Yb 3+ and Er 3+ concentrations based on analysis of spectral and temporal behavior of luminescence. The results indicate that RTET dominates red UC emission for a wide range of dopant concentrations in CaF 2:Er 3+ /Yb 3+ . Furthermore, the origin of the commonly observed decrease of red-to-green intensity ratio on increasing Yb 3+ concentration companied by UC luminescence color change from yellow to green in (Ca, Sr)F 2 is revealed based on the RTET model.

Fields of Study & Subjects

Luminescence Properties of Advanced Materials Luminescence and Fluorescent Materials Nonlinear Optical Materials Studies

Publication details

Journal / source
The Journal of Physical Chemistry Letters
Publisher
American Chemical Society (ACS)
Volume
17
Issue
4
Pages
1077–1084
Publication date
15 January 2026
Language
EN