Red and Time‐Dependent Phosphorescence Color Generated from Cellulose Carbonized Polymer Dots via Precise Core–Shell Structure Modulation

Abstract Achieving red room temperature phosphorescence (RTP) in sustainable materials is attractive but challenging due to the lack of sufficient through‐bond conjugation. Herein, a core–shell structure modulation strategy is proposed to activate red RTP and time‐dependent phosphorescence color (TDPC) in cellulose carbonized polymer dots (CPDs). The CPDs show dual RTP emission species of polymer shell with functional groups and carbon core with conjugation domain, which are responsible for the green RTP at 535 nm and red RTP at 610 nm, respectively. The ratio of the two emission species can be well regulated by modulating the core–shell structure. Whether the core or shell structure dominates RTP, the CPDs display monotonous green or red afterglow. Significantly, the dual RTP emission species can be simultaneously activated by precisely balancing the core–shell structure, leading to dynamic TDPC varying from red to green over time. This work uncovers the origin of core–shell dual emission centers of cellulose CPDs, providing an efficient and simple method toward TDPC and affording a promising sustainable material for information encryption and anti‐counterfeiting.

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Publication Details

Journal
Advanced Functional Materials
Published
2025-09-29
DOI
https://doi.org/10.1002/adfm.202517387
Citations
3
Primary Topic
Carbon and Quantum Dots Applications
Type
article
Field-Weighted Citation Impact
1.55
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article

Red and Time‐Dependent Phosphorescence Color Generated from Cellulose Carbonized Polymer Dots via Precise Core–Shell Structure Modulation

Baozhong Lü, Feng Peng, Zhengjun Shi, Gegu Chen et al.
3 citations
Advanced Functional Materials
Carbon and Quantum Dots Applications
1.55
article

Red and Time‐Dependent Phosphorescence Color Generated from Cellulose Carbonized Polymer Dots via Precise Core–Shell Structure Modulation

Baozhong Lü, Feng Peng, Zhengjun Shi, Gegu Chen, Meichao Shi, Yuetong Kang, Pengyu Li, Mingxing Chen, Qian Gao, Junli Ren
article en
3 citations

Abstract

Abstract Achieving red room temperature phosphorescence (RTP) in sustainable materials is attractive but challenging due to the lack of sufficient through‐bond conjugation. Herein, a core–shell structure modulation strategy is proposed to activate red RTP and time‐dependent phosphorescence color (TDPC) in cellulose carbonized polymer dots (CPDs). The CPDs show dual RTP emission species of polymer shell with functional groups and carbon core with conjugation domain, which are responsible for the green RTP at 535 nm and red RTP at 610 nm, respectively. The ratio of the two emission species can be well regulated by modulating the core–shell structure. Whether the core or shell structure dominates RTP, the CPDs display monotonous green or red afterglow. Significantly, the dual RTP emission species can be simultaneously activated by precisely balancing the core–shell structure, leading to dynamic TDPC varying from red to green over time. This work uncovers the origin of core–shell dual emission centers of cellulose CPDs, providing an efficient and simple method toward TDPC and affording a promising sustainable material for information encryption and anti‐counterfeiting.

Advanced Functional MaterialsVol. 36(16)
Peking University (CN), Southwest Forestry University (CN), Beijing Forestry University (CN), Beijing Chemical Industry Research Institute (China) (CN), South China University of Technology (CN)
Openalex Percentile: Top 16%
Carbon and Quantum Dots Applications
1.55
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