In situ imaging of dealloying during nanoporous gold formation by transmission X-ray microscopy
Source abstract
Abstract
Abstract The dealloying process is directly imaged, for the first time, by using transmission X-ray microscopy for the case of an Ag–30 at.% Au wire dealloyed under free corrosion in nitric acid. The propagation of a sharp dealloying front separating the alloy from nanoporous Au was observed by two-dimensional real-time in situ imaging at 30 nm resolution and measured in detail in three dimensions by an ex situ nanotomography technique at fixed time intervals. The rate of the dealloying front propagation is independent of the dealloying time up to a 3 μm depth, indicating that the dealloying process to this depth is dominated by interfacial effects (i.e. gold surface diffusion and/or silver dissolution) rather than long-range transport effects (i.e. diffusion of acid and corrosion product in and out of the porous layer). The constant dealloying rate corresponds to a constant silver flux and a constant current density, even though the potential might be fluctuating under free corrosion conditions and the interfacial area is shrinking as a function of time. Free corrosion in this system generates a high current density, implying it is driven by a chemical potential difference that is much higher than the critical potential.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Nanoporous metals and alloys · Electrocatalysts for Energy Conversion · Anodic Oxide Films and Nanostructures
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (37)
Show source-provided references
1. Cox · Mater Sci Eng A-Struct Mater Properties Microstruct Process · 2011 · 528 · 240110.1016/j.msea.2010.11.072 ↗
2. Erlebacher · MRS Bull · 2009 · 34 · 610.1557/mrs2009.155 ↗
3. Li · Appl Phys Lett · 2009 · 95
4. Gu · Nano Res · 2009 · 2 · 38610.1007/s12274-009-9038-3 ↗
5. Dixon · Langmuir · 2007 · 23 · 241410.1021/la062313z ↗
6. Qian · Nanotechnology · 2010 · 21 · 7
7. Wada · Mater Lett · 2011 · 65 · 107610.1016/j.matlet.2011.01.054 ↗
8. Zhang · Electrochim Acta · 2009 · 54 · 619010.1016/j.electacta.2009.05.089 ↗
9. Tappan · Angew Chem-Int Ed · 2010 · 49 · 454410.1002/anie.200902994 ↗
10. Ding · MRS Bull · 2009 · 34 · 810.1557/mrs2009.156 ↗
11. Biener · Nat Mater · 2009 · 8 · 4710.1038/nmat2335 ↗
12. Wittstock · Science · 2010 · 327 · 31910.1126/science.1183591 ↗
13. Yu · Adv Mater · 2011 · 23 · 244310.1002/adma.201004331 ↗
14. Lang · Nat Nanotechnol · 2011 · 6 · 23210.1038/nnano.2011.13 ↗
15. Erlebacher · J Electrochem Soc · 2004 · 151 · C61410.1149/1.1784820 ↗
16. Erlebacher · Nature · 2001 · 410 · 45010.1038/35068529 ↗
17. Ding · Adv Mater · 2004 · 16 · 189710.1002/adma.200400792 ↗
18. Dursun · J Electrochem Soc · 2005 · 152 · B6510.1149/1.1848351 ↗
19. Qian · Appl Phys Lett · 2007 · 91
20. Kertis · J Min Met Mater Soc · 2010 · 62 · 5010.1007/s11837-010-0087-6 ↗
21. Erlebacher · Scripta Mater · 2003 · 49 · 99110.1016/S1359-6462(03)00471-8 ↗
22. Pugh · J Electrochem Soc · 2005 · 152 · B45510.1149/1.2048140 ↗
23. Dursun · Electrochem Solid State Lett · 2003 · 6 · B3210.1149/1.1588111 ↗
24. Dursun · J Electrochem Soc · 2003 · 150 · B35510.1149/1.1580824 ↗
25. Pugh · J Mater Res · 2003 · 18 · 21610.1557/JMR.2003.0030 ↗
26. Liu · J Electrochem Soc · 2010 · 157 · K16810.1149/1.3454753 ↗
27. Chen · Nanotechnology · 2008 · 19
28. Chu · Appl Phys Lett · 2008 · 92
29. Zernike · Science · 1955 · 121 · 34510.1126/science.121.3141.345 ↗
30. Natterer · 1986
31. Balluffi · 2005
32. Qian · Appl Phys Lett · 2007 · 90
33. Hakamada · Mater Trans · 2009 · 50 · 43110.2320/matertrans.MBW200825 ↗
34. Qi · J Phys Chem C · 2009 · 113 · 669410.1021/jp810742z ↗
35. Jones · 1995
36. Qian · Appl Phys Lett · 2008 · 92
37. Brandes · 1998