journal article·2019-10Open access

Host–Guest Hybrid Redox Materials Self‐Assembled from Polyoxometalates and Single‐Walled Carbon Nanotubes

Jack W. Jordan, Grace A. Lowe, Robert L. McSweeney, Craig T. Stoppiello, Rhys W. Lodge, Stephen T. Skowron, Johannes Biskupek, Graham A. Rance, Ute Kaiser, Darren A. Walsh, Graham N. Newton, Andrei N. Khlobystov

Advanced Materials· Volume 31· Issue 41

Abstract

Abstract The development of next‐generation molecular‐electronic, electrocatalytic, and energy‐storage systems depends on the availability of robust materials in which molecular charge‐storage sites and conductive hosts are in intimate contact. It is shown here that electron transfer from single‐walled carbon nanotubes (SWNTs) to polyoxometalate (POM) clusters results in the spontaneous formation of host–guest POM@SWNT redox‐active hybrid materials. The SWNTs can conduct charge to and from the encapsulated guest molecules, allowing electrical access to >90% of the encapsulated redox species. Furthermore, the SWNT hosts provide a physical barrier, protecting the POMs from chemical degradation during charging/discharging and facilitating efficient electron transfer throughout the composite, even in electrolytes that usually destroy POMs.
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Research context

OpenAlex topics: Polyoxometalates: Synthesis and Applications · Conducting polymers and applications · Supercapacitor Materials and Fabrication

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

School of Chemistry University of Nottingham Nottingham NG7 2RD UK

GSK Carbon Neutral Laboratories for Sustainable Chemistry University of Nottingham Nottingham NG7 2TU UK

Electron Microscopy Group of Materials Science Ulm University 89081 Ulm Germany

Nanoscale and Microscale Research Centre University of Nottingham Nottingham NG7 2RD UK

Funding

Engineering and Physical Sciences Research Council

References (31)

Show source-provided references
1. 10.1126/science.121274110.1126/science.1212741 ↗
2. 10.1126/science.109067710.1126/science.1090677 ↗
3. 10.1002/adma.20180015910.1002/adma.201800159 ↗
4. 10.1039/B502666K10.1039/B502666K ↗
5. 10.1038/nature1395110.1038/nature13951 ↗
6. 10.1038/s41570-018-011210.1038/s41570-018-0112 ↗
7. 10.1039/C4CP03202K10.1039/C4CP03202K ↗
8. 10.1039/C4EE03749A10.1039/C4EE03749A ↗
9. 10.1038/nchem.76110.1038/nchem.761 ↗
10. 10.1002/adfm.20130162410.1002/adfm.201301624 ↗
11. 10.1039/C5EE03084F10.1039/C5EE03084F ↗
12. 10.1021/nn700250810.1021/nn7002508 ↗
13. 10.1103/PhysRevMaterials.1.07300110.1103/PhysRevMaterials.1.073001 ↗
14. 10.1021/acsnano.7b0222510.1021/acsnano.7b02225 ↗
15. 10.1126/science.289.5483.132410.1126/science.289.5483.1324 ↗
16. 10.1039/C0JM02821E10.1039/C0JM02821E ↗
17. 10.1021/ja105802610.1021/ja1058026 ↗
18. 10.1039/c2sc01026g10.1039/c2sc01026g ↗
19. 10.1021/ja208746z10.1021/ja208746z ↗
20. 10.1021/acs.accounts.7b0007810.1021/acs.accounts.7b00078 ↗
21. 10.1039/b507451g10.1039/b507451g ↗
22. 10.1021/ic50041a03810.1021/ic50041a038 ↗
23. 10.1021/jacs.6b0363310.1021/jacs.6b03633 ↗
24. 10.1021/jp300802z10.1021/jp300802z ↗
25. 10.1002/chem.20160211610.1002/chem.201602116 ↗
26. 10.1039/C8NR00402A10.1039/C8NR00402A ↗
27. 10.1016/S0379-6779(98)00278-110.1016/S0379-6779(98)00278-1 ↗
28. 10.1016/j.pmatsci.2015.09.00110.1016/j.pmatsci.2015.09.001 ↗
29. 10.1021/jp984362t10.1021/jp984362t ↗
30. 10.1021/cr960403a10.1021/cr960403a ↗
31. Bard A. J. · 2001 · 591