journal article·2024-11-08

Sustainable Manufacturing of Vertical Carbon Nanotube (CNT) Arrays Inside Insulating Nanoporous Membranes Using Nickel Magnetic Nanowires (MNWs)

Roman Kolisnyk, Morgen L. Smith, Nicholas C. A. Seaton, Michael L. Odlyzko, Olha Masiuchok, Jeanne Riga, Placidus B. Amama, Bethanie J. H. Stadler

ACS Applied Nano Materials· Volume 7· Issue 21
Publisher page

Abstract

Carbon nanotubes (CNTs) were successfully synthesized using industrial waste gases by chemical vapor deposition inside vertically oriented nanopores of insulating membranes. Importantly, the waste products from Fischer–Tropsch synthesis were used as the carbon source rather than typical purified sources, and this recycling of carbon is important for the sustainability of our environment. Specifically in this work, vertical CNT arrays were achieved using nickel (Ni) magnetic nanowires (MNWs) catalysts that were prepared by template electrochemical deposition inside 50 μm-thick nanoporous anodized aluminum oxide (AAO). Here, the nanopore diameter (20–200 nm) and Ni MNW length (45 and 25 μm) were varied to study the impact on CNT growth characteristics. Raman spectroscopy, scanning electron microscopy, transmission electron microscopy, and field emission spectroscopy were used to characterize CNTs on Ni MNWs. For long MNWs (45 μm), the Ni catalyst was just below the AAO surface, so CNT diameters did not change appreciably with the MNW diameter. Alternatively, for short MNWs (25 μm), the carbon source gases had to diffuse into the AAO nanopores before reacting with the Ni catalyst, and both the CNT diameter and yield increased with the nanopore diameter. Highly crystalline CNTs were formed from particles of Ni catalyst, although for smaller diameter nanopores, the Ni catalyst particle could be blocked by template pore wall defects, resulting in subsequent amorphous nanofiber growth above the blocked particle. Optimally, CNT synthesis was observed for 25 μm MNWs grown in 80 nm AAO nanopores, maximizing field emission current at 480 μA/cm 2 (at electric field 0.5 V/μm) with a turn-on field of 0.26 V/μm.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Carbon Nanotubes in Composites · Nanopore and Nanochannel Transport Studies · Supercapacitor Materials and Fabrication

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

Affiliations

Department of Electrical and Computer Engineering, University of Minnesota, 200 Union St SE, Minneapolis, Minnesota 55455, United States

Tim Taylor Department of Chemical Engineering, Kansas State University, 1701A Platt St, Manhattan, Kansas 66506, United States

Characterization Facility, University of Minnesota, 100 Union St. SE, Minneapolis, Minnesota 55455, United States

E.O. Paton Electric Welding Institute of NAS of Ukraine, Kazymyra Malevycha 11, Kyiv 03680, Ukraine

Directed Energy Directorate

Air Force Research Laboratory

Funding

Air Force Office of Scientific Research

References (59)

Show source-provided references
1. Dresselhaus M. S. · 1996
2. 10.1039/C4TA03022B10.1039/C4TA03022B ↗
3. 10.1038/s41467-024-45142-010.1038/s41467-024-45142-0 ↗
4. 10.1021/acsanm.0c0187910.1021/acsanm.0c01879 ↗
5. 10.1039/c3tc30904e10.1039/c3tc30904e ↗
6. 10.1021/jp107771410.1021/jp1077714 ↗
7. Li J. · 2005 · 300 · 19110.1385/1-59259-858-7:191 ↗
8. 10.3389/fchem.2021.65502510.3389/fchem.2021.655025 ↗
9. 10.3390/s2104122010.3390/s21041220 ↗
10. Correa-Duarte M. A. · 2010
11. 10.3390/polym1509210510.3390/polym15092105 ↗
12. 10.1021/acsami.6b1072610.1021/acsami.6b10726 ↗
13. 10.1021/acsnano.8b0651110.1021/acsnano.8b06511 ↗
14. 10.1126/science.282.5391.110510.1126/science.282.5391.1105 ↗
15. 10.1021/acsnano.2c0223310.1021/acsnano.2c02233 ↗
16. 10.1021/acsanm.9b0183010.1021/acsanm.9b01830 ↗
17. 10.1016/j.vacuum.2019.10907110.1016/j.vacuum.2019.109071 ↗
18. 10.1016/j.jallcom.2019.15264810.1016/j.jallcom.2019.152648 ↗
19. 10.1098/rsta.2004.143810.1098/rsta.2004.1438 ↗
20. 10.1039/D0TC05873D10.1039/D0TC05873D ↗
21. 10.1126/science.270.5239.117910.1126/science.270.5239.1179 ↗
22. 10.1039/b314155c10.1039/b314155c ↗
23. 10.1038/437968a10.1038/437968a ↗
24. 10.1007/s11664-020-08582-010.1007/s11664-020-08582-0 ↗
25. 10.1016/j.tsf.2011.02.04610.1016/j.tsf.2011.02.046 ↗
26. 10.1186/1556-276X-9-54010.1186/1556-276X-9-540 ↗
27. 10.1063/1.12625810.1063/1.126258 ↗
28. 10.1021/cm970412f10.1021/cm970412f ↗
29. 10.1063/1.12491110.1063/1.124911 ↗
30. 10.1021/jp002408o10.1021/jp002408o ↗
31. 10.1038/s41598-020-72094-410.1038/s41598-020-72094-4 ↗
32. 10.1038/s41598-021-83349-z10.1038/s41598-021-83349-z ↗
33. 10.3390/nano1009166210.3390/nano10091662 ↗
34. 10.3109/02656736.2013.83675810.3109/02656736.2013.836758 ↗
35. 10.1063/5.001790310.1063/5.0017903 ↗
36. 10.1016/j.diamond.2021.10880710.1016/j.diamond.2021.108807 ↗
37. 10.1116/1.489878210.1116/1.4898782 ↗
38. 10.1016/S0040-6090(02)00752-610.1016/S0040-6090(02)00752-6 ↗
39. 10.1016/j.diamond.2004.10.01210.1016/j.diamond.2004.10.012 ↗
40. 10.1109/TMAG.2022.321869610.1109/TMAG.2022.3218696 ↗
41. 10.1016/j.pmatsci.2023.10108910.1016/j.pmatsci.2023.101089 ↗
42. 10.1103/PhysRevB.20.39210.1103/PhysRevB.20.392 ↗
43. 10.1002/jrs.212010.1002/jrs.2120 ↗
44. 10.3390/coatings710015310.3390/coatings7100153 ↗
45. 10.1039/C6NR03679A10.1039/C6NR03679A ↗
46. 10.1016/j.carbon.2017.01.09610.1016/j.carbon.2017.01.096 ↗
47. 10.1021/acs.iecr.0c0071110.1021/acs.iecr.0c00711 ↗
48. 10.1063/1.236438110.1063/1.2364381 ↗
49. 10.1002/cvde.20040634710.1002/cvde.200406347 ↗
50. 10.1016/S0008-6223(99)00139-610.1016/S0008-6223(99)00139-6 ↗
51. 10.1016/j.diamond.2009.06.00210.1016/j.diamond.2009.06.002 ↗
52. 10.1016/j.carbon.2004.04.01510.1016/j.carbon.2004.04.015 ↗
53. 10.1021/cm001407610.1021/cm0014076 ↗
54. 10.1016/j.diamond.2004.05.00710.1016/j.diamond.2004.05.007 ↗
55. 10.1016/j.carbon.2005.05.01210.1016/j.carbon.2005.05.012 ↗
56. 10.1002/sia.172610.1002/sia.1726 ↗
57. 10.1063/1.146510910.1063/1.1465109 ↗
58. 10.1063/1.37131710.1063/1.371317 ↗
59. 10.1063/1.156488210.1063/1.1564882 ↗