Process-Mechanized Green Approach to Organic Phosphorescence: From Mechanochemistry Synthesis to 3D Printing
Carbazole-based organic room-temperature phosphorescent (RTP) materials have attracted widespread attention, yet their structural diversification has remained limited due to inherent synthetic constraints. In this work, a dual-mechanical strategy integrating mechanochemical synthesis with 3D-printed processing is introduced. A g-configured benzoindole (Bd[g]) skeleton is efficiently obtained through a solvent-free mechanochemical protocol, enabling rapid and scalable access to high-performance RTP molecular frameworks. When dispersed within a poly(vinyl butyral) (PVB) matrix, Bd[g] derivatives display stable RTP emission as a result of suppressed molecular motion and minimized environmental quenching. Benefiting from the excellent processability of PVB-based composites, the RTP materials are further shaped into customizable 3D-printed architectures featuring persistent phosphorescence, mechanical flexibility, and strong resistance to seawater. This fully mechanical "molecule-to-device" methodology establishes a practical route toward durable organic RTP systems and underscores their potential in marine sensing, underwater imaging, and long-term anticorrosion applications.
Authors
- Э. А. Захидов
- Xiaokun Ding (ORCID: https://orcid.org/0009-0001-8428-8018)
- Feng Li (ORCID: https://orcid.org/0000-0001-5892-6496)
- Meng Guo (ORCID: https://orcid.org/0000-0001-5772-2272)
- Tao Zhuang (ORCID: https://orcid.org/0009-0001-4216-4551)
- Xinyue Xu
- Jing Lv
- Mingliang Sun
- Dong Ding
Institutions
- Academy of Sciences Republic of Uzbekistan (UZ)
- Ministry of Education of the People's Republic of China (CN)
- Qingdao University of Science and Technology (CN)
- Ocean University of China (CN)
Publication Details
- Journal
- The Journal of Physical Chemistry Letters
- Published
- 2026-02-09
- DOI
- https://doi.org/10.1021/acs.jpclett.5c03971
- Primary Topic
- Luminescence and Fluorescent Materials
- Type
- article
- Field-Weighted Citation Impact
- 0.00