Excitation Wavelength‐Dependent Upconversion Luminescence Enhancement in Tm3+‐Doped LiErF4@LiYF4 System Under High Pressure

Author:

Zhang Ling1,Lang Zhongling23,Lu Yang1,Zhao Xu1,Jiang Bin1,Yan Xu1,Sun Peng1,Liu Fengmin1,Zhou Guangdong4,Zhou Mi2,Wang Yanchao2,Liu Xiaomin1ORCID,Lu Geyu1

Affiliation:

1. State Key Laboratory of Integrated Optoelectronics College of Electronic Science and Engineering Jilin University Changchun 130012 P. R. China

2. State Key Laboratory of Superhard Materials Jilin University Changchun 130012 P. R. China

3. Centre for Advanced Optoelectronic Functional Materials Research Key Laboratory of UV‐Emitting Materials and Technology Ministry of Education Northeast Normal University Changchun 130024 P. R. China

4. College of Chemistry Jilin University Changchun 130021 P. R. China

Abstract

AbstractLocal structural engineering is an endogenous approach to modulate upconversion luminescence (UCL) from upstream to meet the needs of specific application scenarios. Herein, high pressure is utilized as a means to modulate the local structure, and the designed LiErF4:0.5%Tm3+@LiYF4 (Er:Tm@Y) nanoparticles with fast energy transfer rates, abundant cross‐relaxation processes, and multiple near‐infrared wavelengths (808, 980, 1530 nm) excitation properties are tailored as local structure‐sensitive hosts. A unique excitation wavelength‐dependent UCL enhancement of Er:Tm@Y upconversion nanoparticles is observed by pressure‐induced local structure distortions. When the pressure of ≈6 GPa is applied, the UCL is enhanced by a factor of 2.6 at 980 nm excitation only. After pressure release, the luminescence diminishes and recovers. Density functional theory calculations show that the symmetry distortion of the LiErF4 crystal reaches a maximum at pressurization to 6 GPa, while a new Er‐4f state emerges, greatly reducing the bandgap from 8.3 to 5.7 eV. Comparative experiments demonstrate that the local symmetry distortion caused by 0.5%Tm3+ doping and the different energy transfer patterns of Er3+ to Tm3+ at different excitations are responsible for this wavelength‐dependent luminescence enhancement.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Jilin Province

Publisher

Wiley

Subject

Atomic and Molecular Physics, and Optics,Electronic, Optical and Magnetic Materials

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