Plasma-Induced Tailoring of Graphene Oxide Surfaces for Electrochemical Applications: Functionalization and Etching
Source abstract
Abstract
This study investigates the use of radio frequency air plasma as an eco-friendly method to rapidly and reversibly tailor the surface properties of graphene oxide (GO) films. We observed a transition from hydrophilic (contact angle ∼55°) to superhydrophilic (<10°) with short plasma exposure, attributed to a synergistic combination of surface modification and etching. Spectroscopic analyses (FTIR, XPS) revealed early stage formation of carbonyl groups and reduction of hydroxyls, while longer treatments induced atomic-level etching (AFM) and structural changes (XRD). This surface engineering enhanced the dielectric properties of GO films but led to reduced aqueous stability. The elucidated interplay between plasma-induced functionalization and etching provides valuable insights for the controlled modification of GO surfaces for various applications, including advanced dielectrics.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Graphene research and applications · Graphene and Nanomaterials Applications · Diamond and Carbon-based Materials Research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Mechanical Engineering
Union College
Department of Chemistry
NY CREATES
Center for Nanophase Materials Sciences
Oak Ridge National Laboratory
Funding
Oak Ridge National Laboratory · Division of Civil, Mechanical and Manufacturing Innovation
References (37)
Show source-provided references
1. 10.1039/c5ta01010a10.1039/c5ta01010a ↗
2. 10.1039/B917103G10.1039/B917103G ↗
3. 10.1038/nchem.214510.1038/nchem.2145 ↗
4. 10.1063/1.494718810.1063/1.4947188 ↗
5. 10.1016/j.apsusc.2018.01.16710.1016/j.apsusc.2018.01.167 ↗
6. 10.1007/s10854-015-3122-010.1007/s10854-015-3122-0 ↗
7. 10.1002/9781119069445.ch1210.1002/9781119069445.ch12 ↗
8. 10.1002/tcr.20150022310.1002/tcr.201500223 ↗
9. 10.1038/nnano.2015.3710.1038/nnano.2015.37 ↗
10. 10.1016/j.carbon.2023.11850110.1016/j.carbon.2023.118501 ↗
11. 10.1016/j.carbon.2017.10.07510.1016/j.carbon.2017.10.075 ↗
12. 10.3390/nano1102038210.3390/nano11020382 ↗
13. 10.1021/acsapm.0c0127010.1021/acsapm.0c01270 ↗
14. 10.1016/j.apsusc.2023.15909210.1016/j.apsusc.2023.159092 ↗
15. 10.1016/j.snb.2024.13552810.1016/j.snb.2024.135528 ↗
16. 10.1016/j.mtener.2017.03.00110.1016/j.mtener.2017.03.001 ↗
17. 10.1039/C6CC04052G10.1039/C6CC04052G ↗
18. 10.1021/jp509182g10.1021/jp509182g ↗
19. 10.1021/acs.jpcc.3c0153410.1021/acs.jpcc.3c01534 ↗
20. 10.1016/j.ensm.2022.05.01810.1016/j.ensm.2022.05.018 ↗
21. 10.1016/j.est.2019.10092310.1016/j.est.2019.100923 ↗
22. 10.1016/j.cplett.2019.06.03210.1016/j.cplett.2019.06.032 ↗
23. 10.1016/j.est.2020.10215010.1016/j.est.2020.102150 ↗
24. 10.1063/1.501213210.1063/1.5012132 ↗
25. 10.1016/j.carbon.2015.09.05610.1016/j.carbon.2015.09.056 ↗
26. 10.1016/j.snb.2021.13065110.1016/j.snb.2021.130651 ↗
27. 10.1007/s10854-021-06123-x10.1007/s10854-021-06123-x ↗
28. 10.1016/j.apsusc.2018.03.24310.1016/j.apsusc.2018.03.243 ↗
29. 10.1038/srep0633410.1038/srep06334 ↗
30. 10.1016/j.apsusc.2018.12.09610.1016/j.apsusc.2018.12.096 ↗
31. 10.1016/j.apsusc.2018.01.16710.1016/j.apsusc.2018.01.167 ↗
32. 10.1016/j.mtla.2022.10144210.1016/j.mtla.2022.101442 ↗
33. 10.1016/j.diamond.2023.11060110.1016/j.diamond.2023.110601 ↗
34. 10.1016/j.colsurfa.2025.13673710.1016/j.colsurfa.2025.136737 ↗
35. 10.1021/cm060258+10.1021/cm060258+ ↗
36. 10.1016/j.carbon.2024.11950710.1016/j.carbon.2024.119507 ↗
37. 10.1021/jp205261810.1021/jp2052618 ↗