Rivet Graphene
Source abstract
Abstract
Large-area graphene has emerged as a promising material for use in flexible and transparent electronics due to its flexibility and optical and electronic properties. The anchoring of transition metal nanoparticles on large-area single-layer graphene is still a challenge. Here, we report an in situ preparation of carbon nano-onion-encapsulated Fe nanoparticles on rebar graphene, which we term rivet graphene. The hybrid film, which allows for polymer-free transfer and is strong enough to float on water with no added supports, exhibits high optical transparency, excellent electric conductivity, and good hole/electron mobility under certain tensile/compressive strains. The results of contact resistance and transfer length indicate that the current in the rivet graphene transistor does not just flow at the contact edge. Carbon nano-onions encapsulating Fe nanoparticles on the surface enhance the injection of charge between rivet graphene and the metal electrode. The anchoring of Fe nanoparticles encapsulated by carbon nano-onions on rebar graphene will provide additional avenues for applications of nanocarbon-based films in transparent and flexible electronics.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Graphene research and applications · Supercapacitor Materials and Fabrication · Graphene and Nanomaterials Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Materials Science and Engineering, Chongqing University, Chongqing 400030, China
School of Materials Science and Engineering, Tianjin Key Laboratory of Composite and Functional Materials, Tianjin University, Tianjin 300350, China
Collaborative Innovation Center of Chemical Science and Engineering, Tianjin 300350, China
Funding
Chongqing Science and Technology Commission, Chongqing People's Municipal Government · Air Force Office of Scientific Research · China Scholarship Council
References (24)
Show source-provided references
1. 10.1038/ncomms958910.1038/ncomms9589 ↗
2. 10.1038/ncomms392010.1038/ncomms3920 ↗
3. 10.1038/srep1191110.1038/srep11911 ↗
4. 10.1039/C4RA14165B10.1039/C4RA14165B ↗
5. 10.1016/j.carbon.2015.07.01110.1016/j.carbon.2015.07.011 ↗
6. 10.1021/nn501132n10.1021/nn501132n ↗
7. 10.1021/nn505792n10.1021/nn505792n ↗
8. 10.1016/S0009-2614(99)01029-510.1016/S0009-2614(99)01029-5 ↗
9. 10.1126/science.117124510.1126/science.1171245 ↗
10. 10.1016/j.physrep.2009.02.00310.1016/j.physrep.2009.02.003 ↗
11. 10.1021/nl801827v10.1021/nl801827v ↗
12. 10.1021/nn303328e10.1021/nn303328e ↗
13. 10.1016/j.apsusc.2007.09.06310.1016/j.apsusc.2007.09.063 ↗
14. 10.1039/C5NR04929F10.1039/C5NR04929F ↗
15. 10.1021/nl904286r10.1021/nl904286r ↗
16. 10.1038/ncomms195510.1038/ncomms1955 ↗
17. 10.1063/1.369162910.1063/1.3691629 ↗
18. 10.1063/1.349180410.1063/1.3491804 ↗
19. 10.1126/science.124435810.1126/science.1244358 ↗
20. 10.1063/1.487570910.1063/1.4875709 ↗
21. 10.1038/nnano.2011.19610.1038/nnano.2011.196 ↗
22. 10.1088/0957-4484/25/1/01400210.1088/0957-4484/25/1/014002 ↗
23. 10.1038/nnano.2008.6710.1038/nnano.2008.67 ↗
24. 10.1021/ja026501x10.1021/ja026501x ↗