Multiresponsive Color-Tunable Phosphorescence With Matrix-Confined Clusters

Lihui Hou , Ting Wang , Siufung Yu , Xuhui Xu , Xue Yu

Aggregate ›› 2025, Vol. 6 ›› Issue (7) : e70071

PDF
Aggregate ›› 2025, Vol. 6 ›› Issue (7) : e70071 DOI: 10.1002/agt2.70071
RESEARCH ARTICLE

Multiresponsive Color-Tunable Phosphorescence With Matrix-Confined Clusters

Author information +
History +
PDF

Abstract

Ultralong organic phosphorescence (UOP) materials have garnered significant interest for applications in advanced optical recording and information encryption. However, it remains a formidable challenge achieving manipulated phosphorescence due to the limited color channels and poorly populated triplet energy levels. Herein, we report a novel multiresponsive organic phosphorescence material, in which the phosphorescence color can be dynamically tuned with stimuli such as radiation duration, concentration, excitation wavelength, time, and temperature. The material is based on the confined 7H-benzo[c]carbazole (BCz) molecules in the polymer matrix, which is achieved through the size-dependent cluster-triggered emission (CTE) mechanism. The BCz molecules form isolated molecules and different-sized clusters in the matrix, resulting in multiple luminescent centers with different energy levels and phosphorescence lifetimes. Through matrix confinement effects, the activation states of the monomers and multiple clusters could be precisely modulated, resulting in temperature-controlled tunable orange-to-green variations. Furthermore, the multiresponsive properties of the material have been used in both civil and military applications through sophisticated mathematical modeling. This work potentially proposes a guiding strategy for the development of multiresponsive UOP materials based on CTE molecules.

Keywords

cluster-triggered emission / multiresponsive phosphorescence / organic phosphorescence / polymer matrix

Cite this article

Download citation ▾
Lihui Hou, Ting Wang, Siufung Yu, Xuhui Xu, Xue Yu. Multiresponsive Color-Tunable Phosphorescence With Matrix-Confined Clusters. Aggregate, 2025, 6(7): e70071 DOI:10.1002/agt2.70071

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

a) S. Xiong, Y. Xiong, D. Wang, et al., “Achieving Tunable Organic Afterglow and UV-Irradiation-Responsive Ultralong Room-Temperature Phosphorescence From Pyridine-Substituted Triphenylamine Derivatives,” Advanced Materials 35 (2023): e2301874. b) D. Li, Z. Liu, M. Fang, et al., “Ultralong Room-Temperature Phosphorescence With Second-Level Lifetime in Water Based on Cyclodextrin Supramolecular Assembly,” ACS Nano 17 (2023): 12895-12902.

[2]

a) D. Li, Y. Yang, J. Yang, et al., “Completely Aqueous Processable Stimulus Responsive Organic Room Temperature Phosphorescence Materials With Tunable Afterglow Color,” Nature Communications 13 (2022): 347. b) W. Xu, G. Huang, Z. Yang, et al., “Nucleic-acid-base Photofunctional Cocrystal for Information Security and Antimicrobial Applications,” Nature Communications 15 (2024): 2561. c) G. Yang, S. Hao, X. Deng, et al., “Efficient Intersystem Crossing and Tunable Ultralong Organic Room-temperature Phosphorescence via Doping Polyvinylpyrrolidone With Polyaromatic Hydrocarbons,” Nature Communications 15 (2024): 4674. d) H. Im, J. Yoon, B. So, et al., “Four-Dimensional Physical Unclonable Functions and Cryptographic Applications Based on Time-Varying Chaotic Phosphorescent Patterns,” ACS Nano 18 (2024): 11703-11716.

[3]

a) G. Yin, W. Lu, J. Huang, et al., “Ultralong excimer phosphorescence by the self-assembly and confinement of terpyridine derivatives in polymeric matrices,” Aggregate 4 (2023): e344. b) D. Wang, J. Gong, Y. Xiong, et al., “Achieving Color-Tunable and Time-Dependent Organic Long Persistent Luminescence via Phosphorescence Energy Transfer for Advanced Anti-Counterfeiting,” Advanced Functional Materials 33 (2023): 2208895. c) Q. Zhang, S. Xu, L. Zhang, L. Yang, and C. Jiang, “Multiemitting Ultralong Phosphorescent Carbonized Polymer Dots via Synergistic Enhancement Structure Design,” Advanced Science 11 (2024): e2400781. d)Q. Gao, M. Shi, J. Rao, et al., “Fully Exploiting Clusterization-Triggered Room Temperature Phosphorescence of Cellulose by Stepwise Rigidification for Long-Lived and Excitation Wavelength-Dependent Afterglows,” Advanced Functional Materials 34 (2024): 2403977.

[4]

a) H. Wang, H. Ma, N. Gan, et al., “Abnormal Thermally-Stimulated Dynamic Organic Phosphorescence,” Nature Communications 15 (2024): 2134. b) J. Wang, Y. Yang, K. Li, L. Zhang, and Z. Li, “Purely Organic Fluorescence Afterglow: Visible-Light-Excitation, Inherent Mechanism, Tunable Color, and Practical Applications With Very Low Cost,” Angewandte Chemie International Edition 62 (2023): e202304020. c) J. Chen, H. Liu, J. Guo, et al., “Robust Luminescent Molecules With High-Level Reverse Intersystem Crossing for Efficient Near Ultraviolet Organic Light-Emitting Diodes,” Angewandte Chemie International Edition 61 (2022): e202116810. d) B. Zhang, B. Li, H. Zhang, et al., “New Wine in Old Bottles: Fully Substituted Arylthio Effect Realizes High-Efficiency Purely Organic Phosphorescence Light-Emitting Diode With Single and Ultra-Stable Spectra Under 2000 cd m−2,” Aggregate 6 (2025): e726.

[5]

a) C. Ji, L. Lai, P. Li, et al., “Organic Dye Assemblies With Aggregation-Induced Photophysical Changes and Their Bio-Applications,” Aggregate 2 (2021): e39. b) G. Jiang, J. Yu, J. Wang, and B. Z. Tang, “Ion−π Interactions for Constructing Organic Luminescent Materials,” Aggregate 3 (2022): e285. c) J. Gu, W. Yuan, K. Chang, et al., “Organic Materials With Ultrabright Phosphorescence at Room Temperature Under Physiological Conditions for Bioimaging,” Angewandte Chemie International Edition 64 (2025): e202415637. d) D. Guo, W. Wang, K. Zhang, et al., “Visible-Light-Excited Robust Room-Temperature Phosphorescence of Dimeric Single-Component Luminophores in the Amorphous State,” Nature Communications 15 (2024): 3598.

[6]

a) S. Cai, H. Ma, H. Shi, et al., “Enabling Long-Lived Organic Room Temperature Phosphorescence in Polymers by Subunit Interlocking,” Nature Communications 10 (2019): 4247. b) H. Shi, W. Yao, W. Ye, et al., “Ultralong Organic Phosphorescence: From Material Design to Applications,” Accounts of Chemical Research 55 (2022): 3445-3459.

[7]

W. Shao and J. Kim, “Metal-Free Organic Phosphors toward Fast and Efficient Room-Temperature Phosphorescence,” Accounts of Chemical Research 55 (2022): 1573-1585.

[8]

a) X. Bi, Y. Shi, T. Peng, et al., “Multi-Stimuli Responsive and Multicolor Adjustable Pure Organic Room Temperature Fluorescence-Phosphorescent Dual-Emission Materials,” Advanced Functional Materials 31 (2021): 2101312. b) Z. Mao, Z. Yang, Y. Mu, et al., “Linearly Tunable Emission Colors Obtained From a Fluorescent–Phosphorescent Dual-Emission Compound by Mechanical Stimuli,” Angewandte Chemie International Edition 54 (2015): 6270-6273.

[9]

a) S. Garain, S. Kuila, B. C. Garain, et al., “Arylene Diimide Phosphors: Aggregation Modulated Twin Room Temperature Phosphorescence From Pyromellitic Diimides,” Angewandte Chemie International Edition 60 (2021): 12323-12327. b) K. Gu, Z. Meng, X. W. Liu, et al., “A Gated Strategy Stabilizes Room-Temperature Phosphorescence,” Aggregate 4 (2023): e337.

[10]

a) J. Yang, Y. Zhang, X. Wu, et al., “Rational Design of Pyrrole Derivatives With Aggregation-Induced Phosphorescence Characteristics for Time-Resolved and Two-Photon Luminescence Imaging,” Nature Communications 12 (2021): 4883. b) Y. Tao, C. Liu, Y. Xiang, et al., “Resonance-Induced Stimuli-Responsive Capacity Modulation of Organic Ultralong Room Temperature Phosphorescence,” Journal of the American Chemical Society 144 (2022): 6946-6953.

[11]

a) J. W. Oh, S. Lee, H. Han, et al., “Dual-Light Emitting 3D Encryption With Printable Fluorescent-Phosphorescent Metal-Organic Frameworks,” Light: Science & Applications 12 (2023): 226. b) J. Han, W. Feng, D. Y. Muleta, et al., “Small-Molecule-Doped Organic Crystals With Long-Persistent Luminescence,” Advanced Functional Materials 29 (2019): 1902503. c) G. Chen, H. Feng, F. Feng, et al., “Photophysical Tuning of Organic Ionic Crystals From Ultralong Afterglow to Highly Efficient Phosphorescence by Variation of Halides,” The Journal of Physical Chemistry Letters 9 (2018): 6305-6311.

[12]

a) Z. He, W. Zhao, J. W. Y. Lam, et al., “White Light Emission From a Single Organic Molecule With Dual Phosphorescence at Room Temperature,” Nature Communications 8 (2017): 416. b) H. Im, J. Yoon, J. Choi, et al., “Chaotic Organic Crystal Phosphorescent Patterns for Physical Unclonable Functions,” Advanced Materials 33 (2021): e2102542. c) W. Zhao, T. S. Cheung, N. Jiang, et al., “Boosting the Efficiency of Organic Persistent Room-Temperature Phosphorescence by Intramolecular Triplet-Triplet Energy Transfer,” Nature Communications 10 (2019): 1595.

[13]

a) A. W. K. Law, T. S. Cheung, J. Zhang, et al., “Sergeant-and-Soldier Effect in an Organic Room-Temperature Phosphorescent Host-Guest System,” Advanced Materials 36 (2024): e2410739. b) Y. Tian, J. Yang, Z. Liu, et al., “Multistage Stimulus-Responsive Room Temperature Phosphorescence Based on Host–Guest Doping Systems,” Angewandte Chemie International Edition 60 (2021): 20259-20263.

[14]

a) Y. Yu, M. S. Kwon, J. Jung, et al., “Room-Temperature-Phosphorescence-Based Dissolved Oxygen Detection by Core-Shell Polymer Nanoparticles Containing Metal-Free Organic Phosphors,” Angewandte Chemie International Edition 56 (2017): 16207-16211. b) K. Chen, Y. Xiong, D. Wang, et al., “A Facile Strategy for Achieving Polymeric Afterglow Materials With Wide Color-Tunability and Persistent Near-Infrared Luminescence,” Advanced Functional Materials 34 (2024): 2312883. c) Y. Zhang, Y. Su, H. Wu, et al., “Large-Area, Flexible, Transparent, and Long-Lived Polymer-Based Phosphorescence Films,” Journal of the American Chemical Society 143 (2021): 13675-13685.

[15]

a) C. Qian, Z. Ma, X. Fu, et al., “More Than Carbazole Derivatives Activate Room Temperature Ultralong Organic Phosphorescence of Benzoindole Derivatives,” Advanced Materials 34 (2022): e2200544. b) L. Gu, H. Shi, L. Bian, et al., “Colour-Tunable Ultra-Long Organic Phosphorescence of a Single-Component Molecular Crystal,” Nature Photonics 13 (2019): 406-411.

[16]

a) C. Kang, S. Tao, F. Yang, et al., “Enabling Carbonized Polymer Dots With Color-Tunable Time-Dependent Room Temperature Phosphorescence Through Confining Carboxyl Dimer Association,” Angewandte Chemie International Edition 63 (2024): e202316527. b) Z. Wang, L. Gao, Y. Zheng, et al., “Four-in-One Stimulus-Responsive Long-Lived Luminescent Systems Based on Pyrene-Doped Amorphous Polymers,” Angewandte Chemie International Edition 61 (2022): e202203254.

[17]

M. Shi, Q. Gao, J. Rao, et al., “Confinement-Modulated Clusterization-Triggered Time-Dependent Phosphorescence Color From Xylan-Carbonized Polymer Dots,” Journal of the American Chemical Society 146 (2024): 1294-1304.

[18]

a) X. Dou, T. Zhu, Z. Wang, et al., “Color-Tunable, Excitation-Dependent, and Time-Dependent Afterglows From Pure Organic Amorphous Polymers,” Advanced Materials 32 (2020): e2004768. b) J. Chen, T. Yu, E. Ubba, et al., “Achieving Dual-Emissive and Time-Dependent Evolutive Organic Afterglow by Bridging Molecules With Weak Intermolecular Hydrogen Bonding,” Advanced Optical Materials 7 (2019): 1801593. c) J. X. Wang, Y. G. Fang, C. X. Li, et al., “Time-Dependent Afterglow Color in a Single-Component Organic Molecular Crystal,” Angewandte Chemie International Edition 59 (2020): 10032-10036. d) Z. Wang, A. Li, Z. Zhao, et al., “Accessing Excitation- and Time-Responsive Afterglows From Aqueous Processable Amorphous Polymer Films Through Doping and Energy Transfer,” Advanced Materials 34 (2022): e2202182. e) J. Chen, X. Zhang, Z. Xie, and B. Liu, “Ultralong Thermally Activated Delayed Fluorescence Based On Intermolecular Charge Transfer Induced by Isomer in Carbazole Derivative,” Aggregate 5 (2024): e638.

[19]

Y. Gao, W. Ye, K. Qiu, et al., “Regulating Isolated-Molecular and Aggregated-State Phosphorescence for Multicolor Afterglow by Photoactivation,” Advanced Materials 35 (2023): e2306501.

[20]

a) T. Yang, Y. Wang, J. Duan, et al., “Time-Dependent Afterglow From a Single Component Organic Luminogen,” Research 2021 (2021): 9757460. b) W. Shi, R. Wang, J. Liu, et al., “Time-Dependent Phosphorescence Color of Carbon Dots in Binary Salt Matrices Through Activations by Structural Confinement and Defects for Dynamic Information Encryption,” Angewandte Chemie International Edition 62 (2023): e202303063.

[21]

H. Li, J. Gu, Z. Wang, et al., “Single-Component Color-tunable Circularly Polarized Organic Afterglow Through Chiral Clusterization,” Nature Communications 13 (2022): 429.

[22]

C. Wang, L. Qu, X. Chen, et al., “Poly(arylene piperidine) Quaternary Ammonium Salts Promoting Stable Long-Lived Room-Temperature Phosphorescence in Aqueous Environment,” Advanced Materials 34 (2022): e2204415.

[23]

K. Chen, Y. Zhang, Y. Lei, et al., “Twofold Rigidity Activates Ultralong Organic High-Temperature Phosphorescence,” Nature Communications 15 (2024): 1269.

[24]

J. Zhang, L. Hu, K. Zhang, et al., “How to Manipulate Through-Space Conjugation and Clusteroluminescence of Simple AIEgens With Isolated Phenyl Rings,” Journal of the American Chemical Society 143 (2021): 9565-9574.

[25]

H. Wang, H. Shi, W. Ye, et al., “Amorphous Ionic Polymers With Color-Tunable Ultralong Organic Phosphorescence,” Angewandte Chemie International Edition 58 (2019): 18776-18782.

[26]

T. Lu and F. Chen, “Multiwfn: A Multifunctional WaveFunction Analyzer,” Journal of Computational Chemistry 33 (2012): 580-592.

RIGHTS & PERMISSIONS

2025 The Author(s). Aggregate published by SCUT, AIEI, and John Wiley & Sons Australia, Ltd.

AI Summary AI Mindmap
PDF

2

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/