Catalytic Purification of Directly Written Nanostructured Pt Microelectrodes
Source abstract
Abstract
In the majority of cases, nanostructures prepared by focused electron beam induced deposition employing an organometallic precursor contain predominantly carbon-based ligand dissociation products. This is unfortunate with regard to using this high-resolution direct-write approach for the preparation of nanostructures for various fields, such as mesoscopic physics, micromagnetism, metaoptical phenomena in the visible spectral range, or others. Following early attempts of postprocessing Pt-based structures prepared by focused electron beam induced deposition at several hundred degrees Celsius in a reactive gas atmosphere, recent work has focused on developing in situ purification processes by using a stationary O2 flux in combination with electron irradiation to oxidize the carbonaceous component of the deposits. Here we show that this purification process is driven by the catalytic activity of Pt and in fact does not rely on the parallel electron irradiation process to function, if the O2 exposure is done in a pulsed fashion. We suggest a multistep cleaning mechanism which results in pure, nanoporous Pt. By suitably chosen beam parameters, high-resolution Pt dot and line structures with dimensions below 10 nm can thus be conveniently obtained. In temperature-dependent resistance measurements, we find the typical metallic behavior of Pt. In low-temperature magnetoresistance measurements, we see clear evidence for weak antilocalization effects and deduce a dephasing length of 234 nm at 1.2 K. We consider this to be a promising starting point for developing this approach into a versatile preparation technique for Pt-based mesoscopic structures, in particular since the purification process can be run in parallel on different deposits. We furthermore anticipate that our results will spur further research on purification approaches for nanostructures prepared by focused electron beam induced deposition containing a catalytically active metal species such as Pd-, Fe-, or Co-based deposits.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Catalytic Processes in Materials Science · Electrocatalysts for Energy Conversion · Electron and X-Ray Spectroscopy Techniques
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Physikalisches Institut, Goethe-Universität, Max-von-Laue-Strasse 1, 60438 Frankfurt am Main, Germany
Institute for Microtechnologies (IMtech), RheinMain University of Applied Sciences, Am Brückweg 26, 65428 Rüsselsheim, Germany
Funding
Deutsche Forschungsgemeinschaft
References (37)
Show source-provided references
1. Tobing L. Y. M. · Nanotechnology · 2013 · 24 · 07530310.1088/0957-4484/24/7/075303 ↗
2. Chandrasekhar V. · Phys. Rev. Lett. · 1991 · 67 · 357810.1103/PhysRevLett.67.3578 ↗
3. Vlad A. · Small · 2008 · 4 · 55710.1002/smll.200700724 ↗
4. Xu J. · Nanoscale Res. Lett. · 2011 · 6 · 52510.1186/1556-276X-6-525 ↗
5. Grzelczak M. · ACS Nano · 2010 · 4 · 359110.1021/nn100869j ↗
6. Jain T. · ACS Nano · 2009 · 3 · 82810.1021/nn900066w ↗
7. van Kouwen L. · Nano Lett. · 2009 · 9 · 214910.1021/nl900717r ↗
8. Fernández-Pacheco A. · Sci. Rep. · 2013 · 3 · 149210.1038/srep01492 ↗
9. Wnuk J. D. · J. Phys. Chem. C · 2009 · 113 · 248710.1021/jp807824c ↗
10. Wnuk J. D. · Surf. Sci. · 2011 · 605 · 25710.1016/j.susc.2010.10.035 ↗
11. Fernández-Pacheco A. · J. Phys. D · 2009 · 42 · 05500510.1088/0022-3727/42/5/055005 ↗
12. Walz M. M. · Phys. Chem. Chem. Phys. · 2011 · 13 · 1733310.1039/c1cp20865a ↗
13. Botman A. · Nanotechnology · 2006 · 17 · 377910.1088/0957-4484/17/15/028 ↗
14. Elbadawi C. · ACS Appl. Mater. Interfaces · 2013 · 5 · 937210.1021/am403167d ↗
15. Mehendale S. · Nanotechnology · 2013 · 24 · 14530310.1088/0957-4484/24/14/145303 ↗
16. Mehendale, S.; Mulders, J. J. L.; Trompenaars, P. H. F.Nanotechnology 2013: Electronic Devices, Fabrication, MEMS, Fluidics and Computation, Technical Proceedings of the 2013 NSTI Nanotechnology Conference and Expo, Washington, DC, May 12–16, 2103;CRC Press:Boca Raton, FL, 2013; pp474–476.
17. Plank H. · ACS Appl. Mater. Interfaces · 2014 · 6 · 101810.1021/am4045458 ↗
18. Geier B. · J. Phys. Chem. C · 2014 · 118 · 1400910.1021/jp503442b ↗
19. Beyer A. D. · Am. J. Phys. · 2005 · 73 · 101410.1119/1.2049284 ↗
20. Porrati F. · J. Appl. Phys. · 2011 · 109 · 06371510.1063/1.3559773 ↗
21. Tanji T. · J. Electron. Microsc. · 1982 · 31 · 300
22. Fitzgerald A. G. · Surf. Interface Anal. · 1990 · 16 · 16310.1002/sia.740160132 ↗
23. De Teresa J. M. · J. Nanomater. · 2009 · 93686310.1155/2009/936863 ↗
24. Silvis-Cividjian N. · Microelectron. Eng. · 2002 · 61 · 69310.1016/S0167-9317(02)00515-4 ↗
25. Kittel, Ch.Introduction to Solid State Physics;Wiley:New York, 1996; p160.
26. Poker D. B. · Phys. Rev. B · 1982 · 26 · 701210.1103/PhysRevB.26.7012 ↗
27. Liu K. · Phys. Rev. B · 1998 · 58 · R1468110.1103/PhysRevB.58.R14681 ↗
28. Greig D. · J. Phys. F · 1972 · 2 · 69910.1088/0305-4608/2/4/014 ↗
29. Hikami S. · Prog. Theor. Phys. · 1980 · 63 · 70710.1143/PTP.63.707 ↗
30. Bao L. · Sci. Rep. · 2012 · 2 · 72610.1038/srep00726 ↗
31. Elliott R. J. · Phys. Rev. · 1954 · 96 · 26610.1103/PhysRev.96.266 ↗
32. Yafet Y. · Phys. Lett. A · 1983 · 98 · 28710.1016/0375-9601(83)90874-5 ↗
33. Zambelli T. · Nature · 1997 · 390 · 49510.1038/37329 ↗
34. Kašpar J. · Catal. Today · 2003 · 77 · 41910.1016/S0920-5861(02)00384-X ↗
35. Mackus A. J. M. · J. Phys. Chem. C · 2013 · 117 · 1078810.1021/jp402260j ↗
36. Mundschau M. · Platinum Met. Rev. · 1991 · 35 · 18810.1595/003214091X354188195 ↗
37. Ertl G. · Phys. Rev. Lett. · 1982 · 49 · 17710.1103/PhysRevLett.49.177 ↗