0 Datasets
0 Files
Get instant academic access to this publication’s datasets.
Yes. After verification, you can browse and download datasets at no cost. Some premium assets may require author approval.
Files are stored on encrypted storage. Access is restricted to verified users and all downloads are logged.
Yes, message the author after sign-up to request supplementary files or replication code.
Join 50,000+ researchers worldwide. Get instant access to peer-reviewed datasets, advanced analytics, and global collaboration tools.
✓ Immediate verification • ✓ Free institutional access • ✓ Global collaborationJoin our academic network to download verified datasets and collaborate with researchers worldwide.
Get Free AccessAbstract We developed a catalyst‐free, atom‐economical interfacial amino‐yne click polymerization to in situ synthesize new aggregation‐induced emission luminogen (AIEgen)‐based free‐standing porous organic polymer films at room temperature. The crystalline properties of POP films were confirmed by powder X‐ray diffraction and high‐resolution transmission electron microscopy. The good porosity of these POP films was proved by their N 2 uptake experiments. The thickness of POP films can be easily regulated from 16 nm to ≈1 μm by adjusting monomer concentration. More importantly, these AIEgen‐based POP films show bright luminescence with high absolute photoluminescent quantum yields up to 37.8 % and good chemical and thermal stability. The AIEgen‐based POP film can encapsulate an organic dye (e.g., Nile red) to further form an artificial light‐harvesting system with a large red‐shift (Δ λ =141 nm), highly efficient energy‐transfer ability ( Φ ET =91 %), and high antenna effect (11.3).
Bo Song, Liang Zhang, Jianwei Sun, Jacky W. Y. Lam, Ben Zhong Tang (2023). In Situ Synthesis of AIEgen‐based Porous Organic Polymer Films by Interfacial Amino‐yne Click Polymerization for Efficient Light‐Harvesting. , 135(18), DOI: https://doi.org/10.1002/ange.202302543.
Datasets shared by verified academics with rich metadata and previews.
Authors choose access levels; downloads are logged for transparency.
Students and faculty get instant access after verification.
Type
Article
Year
2023
Authors
5
Datasets
0
Total Files
0
Language
en
DOI
https://doi.org/10.1002/ange.202302543
Access datasets from 50,000+ researchers worldwide with institutional verification.
Get Free Access