Author
Listed:
- Meichao Shi
(Beijing Forestry University)
- Qian Gao
(Beijing Forestry University)
- Mingxing Chen
(Peking University)
- Ziwen Lv
(Beijing Forestry University)
- Jun Rao
(Beijing Forestry University)
- Gegu Chen
(Beijing Forestry University)
- Baozhong Lü
(Beijing Forestry University)
- Wei Qi
(Chinese Academy of Sciences)
- Junli Ren
(South China University of Technology)
- Feng Peng
(Beijing Forestry University
State Key Laboratory of Efficient Production of Forest Resources)
Abstract
Time-dependent phosphorescence color is attractive for various applications; however, the modulation mechanism of multiple luminescence centers is still confused. Herein, we proposed a hierarchical luminescence center coupling strategy to develop self-protective xylan carbonized polymer dots with time-dependent phosphorescence color. When using 1,3-diaminopropane as the cross-linker, the polymer dots feature a highly stable and rigid architecture, the clusterization-triggered phosphorescence of which is fully exploited to form hierarchical core−shell phosphorescence centers with different afterglow colors. The core with blue afterglow is dominant at first, and the shell with yellow-green afterglow becomes dominant over time, leading to a typical time-dependent phosphorescence color evolution with large color contrast. The eco-friendly xylan carbonized polymer dots with high contrast time-dependent phosphorescence color can be used for advanced dynamic information encryption and anti-counterfeiting. This work provides an effective method to achieve time-dependent phosphorescence color, and gives insights into the phosphorescence mechanism of carbonized polymer dots.
Suggested Citation
Meichao Shi & Qian Gao & Mingxing Chen & Ziwen Lv & Jun Rao & Gegu Chen & Baozhong Lü & Wei Qi & Junli Ren & Feng Peng, 2025.
"Hierarchical luminescence center coupling enables time-dependent phosphorescence color from self-protective carbonized polymer dots,"
Nature Communications, Nature, vol. 16(1), pages 1-10, December.
Handle:
RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-62807-6
DOI: 10.1038/s41467-025-62807-6
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