Author
Listed:
- Xue Chen
(Northwestern Polytechnical University)
- Zhenyu Gong
(Northwestern Polytechnical University)
- Chenxi Peng
(Northwestern Polytechnical University)
- Tian Bai
(Northwest Institute for Non-Ferrous Metal Research)
- Zhongbin Wu
(Northwestern Polytechnical University)
- Weidong Xu
(Northwestern Polytechnical University)
- Xiaowang Liu
(Northwestern Polytechnical University)
- Wei Huang
(Northwestern Polytechnical University
Nanjing University of Posts & Telecommunications
Nanjing Tech University (Nanjing Tech))
Abstract
Developing monodisperse microparticles with tailored afterglow properties is crucial for optoelectronic applications, achieving afterglow tuning in uniform microsized platforms remains a significant challenge. Here, we present programmable afterglow tuning in monodisperse SiO2 MPs through spatially confined emitter doping, creating core@shell@shell SiO2 MPs. By repeatedly performing pseudomorphic transformation, we achieve spatially confined doping of 4-phenylpyridine, 4,4’-bipyridine, and 1,8-naphthalimide into different layers. This method enables afterglow color output from blue to cyan and orange by shifting main excitation from 250 to 350 nm. It also allows tuning of afterglow lifetime and quantum yields of the dopants by gradually enhancing dopant-matrix interactions through repeating hydrothermal reactions. Additionally, altering the doping positions further controls the optical properties due to a combined screen effect by the outer SiO2 matrix and dopants. Our approach enables the creation of a versatile library of optically active SiO2 MPs with finely tuned properties, paving the way for advanced photonic crystal platforms for optical encoding and spontaneous emission regulation.
Suggested Citation
Xue Chen & Zhenyu Gong & Chenxi Peng & Tian Bai & Zhongbin Wu & Weidong Xu & Xiaowang Liu & Wei Huang, 2025.
"Programmable afterglow tuning in monodisperse SiO2 microparticles through spatially confined emitter doping,"
Nature Communications, Nature, vol. 16(1), pages 1-10, December.
Handle:
RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-63901-5
DOI: 10.1038/s41467-025-63901-5
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