Graphene Nucleation Preferentially at Oxygen‐Rich Cu Sites Rather Than on Pure Cu Surface
Source abstract
Abstract
Graphene nucleation at oxygen-rich Cu sites instead of on the commonly assumed pure Cu surface is discovered using high-spatial-resolution scanning Auger electron microscopy, which reveals a strong O signal existing underneath the graphene seeds, along with density functional theory calculations. 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: Graphene research and applications · Advancements in Battery Materials · ZnO doping and properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Silicon Materials Department of Polymer Science and Engineering Zhejiang University Hangzhou 310027 P. R. China
Department of Chemistry Zhejiang University Hangzhou 310027 P. R. China
Surface and Microbeam Analysis Materials Analysis Station National Institute for Materials Science Tsukuba 305‐0047 Japan
Nano Characterization Unit National Institute for Materials Science Tsukuba 305‐0047 Japan
Funding
National Natural Science Foundation of China
References (36)
Show source-provided references
1. 10.1021/jz301029g10.1021/jz301029g ↗
2. 10.1021/nn304929710.1021/nn3049297 ↗
3. 10.1021/jp507021510.1021/jp5070215 ↗
4. 10.1021/jp410142r10.1021/jp410142r ↗
5. 10.1021/nn300896510.1021/nn3008965 ↗
6. 10.1126/science.117124510.1126/science.1171245 ↗
7. 10.1126/science.124387910.1126/science.1243879 ↗
8. 10.1021/jp404764810.1021/jp4047648 ↗
9. 10.1021/nn505982610.1021/nn5059826 ↗
10. 10.1039/c3tc31717j10.1039/c3tc31717j ↗
11. 10.1021/nl300297410.1021/nl3002974 ↗
12. 10.1002/adfm.20130216610.1002/adfm.201302166 ↗
13. 10.1021/nn100276w10.1021/nn100276w ↗
14. 10.1088/0957-4484/21/26/26570510.1088/0957-4484/21/26/265705 ↗
15. 10.1039/c1nr10294j10.1039/c1nr10294j ↗
16. 10.1016/0039-6028(77)90353-310.1016/0039-6028(77)90353-3 ↗
17. Bomermann J. · Surf. Sci. · 1996 · 357 · 894
18. 10.1023/A:102362742472310.1023/A:1023627424723 ↗
19. 10.1021/nl201980p10.1021/nl201980p ↗
20. 10.1021/nn404393b10.1021/nn404393b ↗
21. 10.1039/C4TA01975J10.1039/C4TA01975J ↗
22. 10.1021/nn401435610.1021/nn4014356 ↗
23. 10.1021/nl503646310.1021/nl5036463 ↗
24. 10.1063/1.162577910.1063/1.1625779 ↗
25. 10.1021/nn100023h10.1021/nn100023h ↗
26. 10.1039/c3cp55503h10.1039/c3cp55503h ↗
27. 10.1039/c3cp52318g10.1039/c3cp52318g ↗
28. 10.1016/0021-9517(78)90068-410.1016/0021-9517(78)90068-4 ↗
29. Sexton B. A. · Appl. Surf. Sci. · 1985 · 22 · 404
30. 10.1039/b000253o10.1039/b000253o ↗
31. 10.1016/j.carbon.2013.12.03210.1016/j.carbon.2013.12.032 ↗
32. 10.1021/ja206363310.1021/ja2063633 ↗
33. 10.1021/ja107855q10.1021/ja107855q ↗
34. 10.1557/jmr.2013.38810.1557/jmr.2013.388 ↗
35. 10.1038/ncomms309610.1038/ncomms3096 ↗
36. 10.1088/2053-1583/2/1/01400610.1088/2053-1583/2/1/014006 ↗