journal article·2018-09-28Open access

Enhancing Graphene Protective Coatings by Hydrogen-Induced Chemical Bond Formation

Line Kyhl, Richard Balog, Andrew Cassidy, Jakob Jørgensen, Antonija Grubisic-Čabo, Lena Trotochaud, Hendrik Bluhm, Liv Hornekær

ACS Applied Nano Materials· Volume 1· Issue 9

Abstract

Increased interactions at the graphene-metal interface are here demonstrated to yield an effective prevention of intercalation of foreign species below the graphene cover. Hereby, an engineering pathway for increasing the usability of graphene as a metal coating is demonstrated. Graphene on Ir(111) (Gr/Ir(111)) is used as a model system, as it has previously been well-established that an increased interaction and formation of chemical bonds at the graphene-Ir interface can be induced by hydrogen functionalization of the graphene from its top side. With X-ray photoelectron spectroscopy, it is shown that hydrogen-induced increased interactions at the Gr/Ir(111) interface effectively prevents intercalation of CO in the millibar range. The scheme leads to protection against at least 10 times higher pressure and 70 times higher fluences of CO, compared to the protection offered by pristine Gr/Ir(111).
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Graphene research and applications · Advancements in Battery Materials · Graphene and Nanomaterials Applications

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

Affiliations

Chemical Sciences Division, Lawrence Berkeley National Lab, Berkeley, California 94720, United States

Funding

Basic Energy Sciences · Det Frie Forskningsr?d · Villum Fonden · H2020 European Research Council · Innovationsfonden

References (42)

Show source-provided references
1. 10.1126/science.110289610.1126/science.1102896 ↗
2. 10.1038/ncomms753910.1038/ncomms7539 ↗
3. 10.1103/PhysRevB.85.15544510.1103/PhysRevB.85.155445 ↗
4. 10.1016/j.corsci.2011.12.00310.1016/j.corsci.2011.12.003 ↗
5. 10.1021/nn203507y10.1021/nn203507y ↗
6. 10.1039/C4FD00259H10.1039/C4FD00259H ↗
7. 10.1021/nl801384y10.1021/nl801384y ↗
8. 10.1126/science.115696510.1126/science.1156965 ↗
9. 10.1021/nn103028d10.1021/nn103028d ↗
10. 10.1039/C3NR05997A10.1039/C3NR05997A ↗
11. 10.1166/sam.2014.177610.1166/sam.2014.1776 ↗
12. 10.1002/anie.20120041310.1002/anie.201200413 ↗
13. 10.1021/nn304058810.1021/nn3040588 ↗
14. 10.1021/jz402054e10.1021/jz402054e ↗
15. 10.1063/1.284180910.1063/1.2841809 ↗
16. 10.1016/j.carbon.2014.07.01510.1016/j.carbon.2014.07.015 ↗
17. 10.1088/0953-8984/21/13/13400210.1088/0953-8984/21/13/134002 ↗
18. 10.1063/1.295397210.1063/1.2953972 ↗
19. 10.1088/0957-4484/22/16/16570110.1088/0957-4484/22/16/165701 ↗
20. 10.1063/1.487100010.1063/1.4871000 ↗
21. 10.1063/1.486811910.1063/1.4868119 ↗
22. 10.1038/ncomms377210.1038/ncomms3772 ↗
23. 10.1063/1.479586110.1063/1.4795861 ↗
24. 10.1021/nn404756q10.1021/nn404756q ↗
25. 10.1021/nn401435610.1021/nn4014356 ↗
26. 10.1016/j.jpowsour.2015.06.00910.1016/j.jpowsour.2015.06.009 ↗
27. 10.1021/jacs.5b0872910.1021/jacs.5b08729 ↗
28. 10.1021/jp404304510.1021/jp4043045 ↗
29. 10.1088/1361-648X/29/5/05300210.1088/1361-648X/29/5/053002 ↗
30. 10.1021/jp503485510.1021/jp5034855 ↗
31. 10.1103/PhysRevLett.107.03610110.1103/PhysRevLett.107.036101 ↗
32. 10.1063/1.352423210.1063/1.3524232 ↗
33. 10.1088/1367-2630/10/4/04303310.1088/1367-2630/10/4/043033 ↗
34. 10.1038/nmat271010.1038/nmat2710 ↗
35. 10.1103/PhysRevB.93.11540310.1103/PhysRevB.93.115403 ↗
36. 10.1021/acsnano.6b0467110.1021/acsnano.6b04671 ↗
37. 10.1021/nn400780x10.1021/nn400780x ↗
38. 10.1021/acsnano.7b0707910.1021/acsnano.7b07079 ↗
39. 10.1103/PhysRevLett.96.15610410.1103/PhysRevLett.96.156104 ↗
40. 10.1103/PhysRevLett.102.05680810.1103/PhysRevLett.102.056808 ↗
41. 10.1103/PhysRevLett.103.16610110.1103/PhysRevLett.103.166101 ↗
42. 10.1088/0022-3719/3/2/01010.1088/0022-3719/3/2/010 ↗