Photon Upconversion at Crystalline Organic–Organic Heterojunctions
Source abstract
Abstract
Triplet transfer across a surface-anchored metal–organic-framework heterojunction is demonstrated by the observation of triplet–triplet annihilation photon upconversion in a sensitizer–emitter heterostructure. Upconversion thresholds under 1 mW cm−2 are achieved. In the broader context, the double-electron-exchange mechanism of triplet transfer indicates that the heterojunction quality is sufficient for electrons to move between layers in this solution-processed crystalline heterostructure. As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Luminescence and Fluorescent Materials · Lanthanide and Transition Metal Complexes · Luminescence Properties of Advanced Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Karlsruhe Institute of Technology Institute of Microstructure Technology (IMT) Hermann‐von‐Helmholtz‐Platz 1 76344 Eggenstein‐Leopoldshafen Germany
Karlsruhe Institute of Technology Institute of Functional Interfaces (IFG) Hermann‐von‐Helmholtz‐Platz 1 76344 Eggenstein‐Leopoldshafen Germany
Karlsruhe Institute of Technology Karlsruhe Nano Micro Facility (KNMF) Hermann‐von‐Helmholtz‐Platz 1 76344 Eggenstein‐Leopoldshafen Germany
Funding
Carl-Zeiss-Stiftung
References (24)
Show source-provided references
1. 10.1038/nchem.83410.1038/nchem.834 ↗
2. 10.1038/nmat411310.1038/nmat4113 ↗
3. 10.1038/ncomms626110.1038/ncomms6261 ↗
4. 10.1021/ja206029a10.1021/ja206029a ↗
5. 10.1021/ja310596a10.1021/ja310596a ↗
6. 10.1021/jacs.6b0165210.1021/jacs.6b01652 ↗
7. 10.1038/nmat436610.1038/nmat4366 ↗
8. 10.1126/science.124673810.1126/science.1246738 ↗
9. 10.1002/adma.20150107810.1002/adma.201501078 ↗
10. 10.1039/c2cp23900k10.1039/c2cp23900k ↗
11. 10.1039/C4EE02481H10.1039/C4EE02481H ↗
12. 10.1039/c2sc20065a10.1039/c2sc20065a ↗
13. 10.1002/adfm.20110159210.1002/adfm.201101592 ↗
14. 10.1021/nl404767k10.1021/nl404767k ↗
15. 10.1039/c4qi00037d10.1039/c4qi00037d ↗
16. 10.1002/anie.20150186210.1002/anie.201501862 ↗
17. 10.1002/anie.20110424010.1002/anie.201104240 ↗
18. 10.1038/srep0092110.1038/srep00921 ↗
19. 10.1103/PhysRevB.81.16520810.1103/PhysRevB.81.165208 ↗
20. 10.1038/srep1088210.1038/srep10882 ↗
21. 10.1016/j.micromeso.2015.02.04810.1016/j.micromeso.2015.02.048 ↗
22. 10.1007/978-0-387-46312-410.1007/978-0-387-46312-4 ↗
23. 10.1021/jacs.6b0270010.1021/jacs.6b02700 ↗
24. 10.1002/adma.1997009030810.1002/adma.19970090308 ↗