journal article·2024-05Open access

Quantum Dot Modification of Large Area Graphene Surfaces via Amide Bonding

T. J. Neubert, F. Rösicke, K. Hinrichs, N. H. Nickel, J. Rappich

Advanced Materials Interfaces· Volume 11· Issue 15

Abstract

Abstract Large‐area graphene grown by chemical vapor deposition is functionalized by p‐aminophenyl groups via the diazonium‐route. Subsequently, carboxylic acid‐modified CdSXSe1‐X/ZnS dots (QDs) with maximum emission wavelengths of 540 nm and 630 nm are immobilized via amidation reaction to the amino‐functionalized graphene on the copper growth substrate forming stable covalent bonds in all functionalization steps. After immobilization of the QDs, the functional QD/graphene stack is available for transfer from the growth substrate onto any other substrate. In this study, the QD‐modified graphene is transferred to a Si wafer with surface oxide without losing the QD modification. The successful binding of the QDs onto the functionalized graphene is characterized by their vibrational signature using Raman backscattering and infrared‐spectroscopic ellipsometry and by their specific light emission as measured by photoluminescence (PL) spectroscopy.
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Research context

OpenAlex topics: Graphene research and applications · Quantum Dots Synthesis And Properties · Graphene and Nanomaterials Applications

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

Affiliations

Department of Chemistry Laboratory for Organic Synthesis of Functional Systems Humboldt‐Universität zu Berlin Brook‐Taylor‐Str. 2 12489 Berlin Germany

Bayer AG Kaiser‐Wilhelm‐Allee 1 51373 Leverkusen Germany

Leibniz‐Institut für Analytische Wissenschaften – ISAS – e. V. Application Labs Berlin Schwarzschildstr. 8 12489 Berlin Germany

Young Investigator Group Nanoscale Solid‐Liquid Interfaces Helmholtz‐Zentrum Berlin für Materialien und Energie GmbH Schwarzschildstr. 8 12489 Berlin Germany

References (37)

Show source-provided references
1. 10.1021/acsanm.8b0052010.1021/acsanm.8b00520 ↗
2. 10.1021/ja061131o10.1021/ja061131o ↗
3. 10.1002/jps.260069072510.1002/jps.2600690725 ↗
4. 10.1016/j.memsci.2003.12.00510.1016/j.memsci.2003.12.005 ↗
5. 10.1039/c0cs00056f10.1039/c0cs00056f ↗
6. 10.1039/b517613c10.1039/b517613c ↗
7. 10.1021/ja066658f10.1021/ja066658f ↗
8. Sai H. T. · Analytical Sciences · 2001 · 17 · 269
9. 10.1039/c2nr30915g10.1039/c2nr30915g ↗
10. 10.1002/chem.20130344610.1002/chem.201303446 ↗
11. 10.1002/aenm.20130192510.1002/aenm.201301925 ↗
12. 10.1002/aenm.20150001010.1002/aenm.201500010 ↗
13. 10.1002/smll.20090237010.1002/smll.200902370 ↗
14. 10.3390/bios201000110.3390/bios2010001 ↗
15. 10.1002/anie.20150147310.1002/anie.201501473 ↗
16. 10.1039/C7CC03951D10.1039/C7CC03951D ↗
17. 10.1021/acsami.0c1455910.1021/acsami.0c14559 ↗
18. Hinrichs K. · Encycl. Interfacial Chem. Surf. Sci. Electrochem. · 2018 · 80
19. Leenaerts O. · 2013
20. 10.1088/0953-8984/26/44/44300110.1088/0953-8984/26/44/443001 ↗
21. 10.1021/acsami.6b1321110.1021/acsami.6b13211 ↗
22. 10.1016/j.apsusc.2017.04.23510.1016/j.apsusc.2017.04.235 ↗
23. 10.1002/jmr.239610.1002/jmr.2396 ↗
24. 10.1021/ja00040a07410.1021/ja00040a074 ↗
25. 10.1039/c0cs00149j10.1039/c0cs00149j ↗
26. 10.1039/b406228k10.1039/b406228k ↗
27. 10.1016/j.elecom.2010.07.03210.1016/j.elecom.2010.07.032 ↗
28. 10.1002/appl.20220005410.1002/appl.202200054 ↗
29. 10.1039/c0cp00058b10.1039/c0cp00058b ↗
30. 10.1515/zpch-2014-045010.1515/zpch-2014-0450 ↗
31. 10.1038/nchem.142110.1038/nchem.1421 ↗
32. 10.1021/nn901570m10.1021/nn901570m ↗
33. 10.1021/jacs.8b0875310.1021/jacs.8b08753 ↗
34. 10.1016/S0022-2313(99)00363-410.1016/S0022-2313(99)00363-4 ↗
35. 10.1038/nature2142410.1038/nature21424 ↗
36. 10.1002/prac.1990332021610.1002/prac.19903320216 ↗
37. 10.1149/2.044210jes10.1149/2.044210jes ↗