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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.
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http://dx.doi.org/10.1038/s41467-025-62807-6 | DOI Listing |
Small
September 2025
Department of Applied Biology and Chemical Technology and Research Institute for Smart Energy, The Hong Kong Polytechnic University, Hong Kong, 999077, P. R. China.
The precise modulation of the lifetime and the responsive properties of room-temperature phosphorescence (RTP) is essential for realizing its multifunctional applications. Herein, a facile strategy is presented to achieve a series of cellulose benzoate esters (CBE-X, X = H/CH/OH/NH) with lifetime-tunable RTP through substituent engineering. Enhancing the electron-donating ability of CBE-X effectively modulates the HOMO-LUMO gap, exciton energy, spin-orbit coupling, and interaction between cellulose chains, thereby enabling control over the RTP lifetime.
View Article and Find Full Text PDFSpectrochim Acta A Mol Biomol Spectrosc
August 2025
Shanxi Normal University, Taiyuan 030031, PR China. Electronic address:
Visible light is a more accessible and less phototoxic excitation light source in practical applications than ultraviolet light. However, it's still a challenge to prepare visible-light-excited carbon-dot long-afterglow photochromic materials. In this study, a carbon dots/boronic acid composite (CDs/BA) based on boron-carbon bond (BC) was synthesized.
View Article and Find Full Text PDFNat Commun
August 2025
Beijing Key Laboratory of Lignocellulosic Chemistry, MOE Engineering Research Center of Forestry Biomass Materials and Bioenergy, College of Materials Science and Technology, Beijing Forestry University, Beijing, 100083, China.
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.
View Article and Find Full Text PDFSmall
July 2025
State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, Beijing, 100029, China.
The development of eco-friendly time-dependent phosphorescent color (TDPC) materials faces a critical paradox: Boron oxide (BO) derived from commercial boric acid (BO-) exhibits stable room-temperature phosphorescence (RTP) regardless of purity, while ultrapure synthetic analogs remain non-emissive. Here, this dilemma is resolved by engineering carbon dots (CDs) doped into BO- at ultralow concentrations (10 ppb), achieving programmable TDPC through three breakthroughs. Synergistic host-guest confinement amplifies green RTP efficiency by an order of magnitude enhancement while activating yellow guest emission; Defect-mediated exciton transfer extends RTP lifetimes to 304 ms, doubling BO-; Time-resolved chromatic evolution (Δλ = 65 nm) emerges exclusively in doped systems, enabled by bifurcated decay kinetics from dual confinement mechanisms.
View Article and Find Full Text PDFNano Lett
July 2025
Beijing Key Laboratory of Lignocellulosic Chemistry, MOE Engineering Research Center of Forestry Biomass Materials and Bioenergy, College of Materials Science and Technology, Beijing Forestry University, Beijing 100083, China.
Bioplastics are developed to replace petrochemical-based plastics to address environmental pollution, but their practicality is limited (e.g., mechanical performance, cost, and wet stability).
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