Author
Listed:
- Wensheng Xu
(Tianjin University)
- Bowei Wang
(Tianjin University
Zhejiang Institute of Tianjin University
Collaborative Innovation Center of Chemical Science and Engineering (Tianjin)
Tianjin Engineering Research Center of Functional Fine Chemicals)
- Shuai Liu
(Shaoxing Xingxin New Materials Co., Ltd)
- Wangwang Fang
(Tianjin University
Zhejiang Institute of Tianjin University
Shaoxing Xingxin New Materials Co., Ltd)
- Qinglong Jia
(Tianjin University)
- Jiayi Liu
(Tianjin University)
- Changchang Bo
(Tianjin University)
- Xilong Yan
(Tianjin University
Zhejiang Institute of Tianjin University
Collaborative Innovation Center of Chemical Science and Engineering (Tianjin)
Tianjin Engineering Research Center of Functional Fine Chemicals)
- Yang Li
(Tianjin University
Collaborative Innovation Center of Chemical Science and Engineering (Tianjin))
- Ligong Chen
(Tianjin University
Zhejiang Institute of Tianjin University
Collaborative Innovation Center of Chemical Science and Engineering (Tianjin)
Tianjin Engineering Research Center of Functional Fine Chemicals)
Abstract
Organic room-temperature phosphorescence materials have attracted extensive attention, but their development is limited by the stability and processibility. Herein, based on the on-line derivatization strategy, we report the urea-formaldehyde room-temperature phosphorescence materials which are constructed by polycondensation of aromatic diamines with urea and formaldehyde. Excitingly, urea-formaldehyde room-temperature phosphorescence materials achieve phosphor lifetime up to 3326 ms. There may be two ways to enhance phosphorescence performance, one is that the polycondensation of aromatic diamine with urea and formaldehyde promotes spin-orbit coupling, and another is that the imidazole derivatives derived from the condensation of aromatic o-diamine with formaldehyde maintains low levels of energy level difference and spin-orbit coupling, thus achieving ultra-long afterglow. Surprisingly, urea-formaldehyde room-temperature phosphorescence materials exhibit tunable phosphorescence emission in electrostatic field. Accordingly, 1,4-phenylenediamine, urea, and formaldehyde are copolymerized and self-assembled into phosphorescence microspheres with different electrostatic potential strengths. By mixing 1 wt% 1,4-phenylenediamine polycondensation microspheres with 1,4-phenylenediamine free microspheres, phosphor lifetime of the composite could be regulated from 27 ms to 123 ms. Moreover, vulcanization process enables precise shaping of urea-formaldehyde room-temperature phosphorescence materials. This work not only demonstrates that urea-formaldehyde room-temperature phosphorescence materials are promising candidates for organic phosphors, but also exhibits the phenomenon of electrostatically regulated phosphorescence.
Suggested Citation
Wensheng Xu & Bowei Wang & Shuai Liu & Wangwang Fang & Qinglong Jia & Jiayi Liu & Changchang Bo & Xilong Yan & Yang Li & Ligong Chen, 2024.
"Urea-formaldehyde resin room temperature phosphorescent material with ultra-long afterglow and adjustable phosphorescence performance,"
Nature Communications, Nature, vol. 15(1), pages 1-10, December.
Handle:
RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-48744-w
DOI: 10.1038/s41467-024-48744-w
Download full text from publisher
Most related items
These are the items that most often cite the same works as this one and are cited by the same works as this one.
- Xing Wang Liu & Weijun Zhao & Yue Wu & Zhengong Meng & Zikai He & Xin Qi & Yiran Ren & Zhen-Qiang Yu & Ben Zhong Tang, 2022.
"Photo-thermo-induced room-temperature phosphorescence through solid-state molecular motion,"
Nature Communications, Nature, vol. 13(1), pages 1-8, December.
- Lei Ge & Yikai Tang & Chongzhi Wang & Jian Chen & Hui Mao & Xiqun Jiang, 2024.
"A light-activatable theranostic combination for ratiometric hypoxia imaging and oxygen-deprived drug activity enhancement,"
Nature Communications, Nature, vol. 15(1), pages 1-12, December.
Corrections
All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-48744-w. See general information about how to correct material in RePEc.
If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.
If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .
If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.
For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .
Please note that corrections may take a couple of weeks to filter through
the various RePEc services.