Mutual energy transfer luminescent properties in novel CsGd(MoO4)2:Yb3+,Er3+/Ho3+ phosphors for solid-state lighting and solar cells

Literature Information

Publication Date 2018-11-27
DOI 10.1039/C8CP06538A
Impact Factor 3.676
Authors

Kai Li, Rik Van Deun


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Abstract

In this work, we prepared a novel kind of Yb3+,Er3+/Ho3+ co-doped CsGd(MoO4)2 phosphors with a different structure from the reported ALn(MoO4)2 (A = Li, Na or K; Ln = La, Gd or Y) compounds using a high-temperature solid-state reaction method. X-ray diffraction showed that the as-prepared samples had a pure phase. Based on the efficient energy transfer from Yb3+ to Er3+/Ho3+, the up-conversion (UC) luminescence of the optimal CsGd(MoO4)2:0.30Yb3+,0.02Er3+ sample showed intensely green light with dominant emission peaks at 528 and 550 nm corresponding to Er3+ transitions 2H11/2 → 4I15/2 and 4S3/2 → 4I15/2, respectively, as well as a weak emission peak originating from 4F9/2 → 4I15/2 at 671 nm, under 975 nm laser excitation. The CsGd(MoO4)2:Yb3+,Ho3+ samples mainly displayed two emission bands around 540 and 660 nm together with a negligible one at 755 nm, which corresponded to Ho3+ transitions 4F4,5F2 → 5I8, 5F5 → 5I8 and 4F4,5F2 → 5I7, respectively, under 975 nm laser excitation. With increasing Yb3+ concentration in CsGd(MoO4)2:Yb3+,Ho3+ phosphors, the emission color could be tuned from orange red to light yellow due to the large energy gap between levels 4F4,5F2 and 5F5. In addition, the CsGd(MoO4)2:Yb3+,Er3+ showed green light under 376 nm UV irradiation similar to that upon 975 nm laser excitation. However, the emissions for CsGd(MoO4)2:Yb3+,Ho3+ samples under 358 nm UV or 449 nm blue excitation showed dominant emission peaks at 540 nm and weak 660 nm and 752 nm peaks, which were a bit different from those under 975 nm excitation. Interestingly, we observed efficient energy transfer phenomena (possible quantum cutting) from Er3+/Ho3+ to Yb3+ and a Yb3+–O2− charge transfer (CT) transition in the molybdates, which was deduced from the visible and near-infrared emission spectra and the decrease of the Er3+/Ho3+ luminescent lifetimes with increasing Yb3+ concentration in the CsGd(MoO4)2:Yb3+,Er3+/Ho3+ samples. The luminescence properties of these phosphors suggest their potential possibility for applications in solid-state lighting and displays as well as in c-Si solar energy conversion systems.

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Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics
CiteScore: 5.5
Self-citation Rate: 10.3%
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Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.

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