journal article·2023-11

Ni2+‐Assisted Dealloying Strategy to Prepare Nanoporous Cu–Ni Alloys with Enhanced Corrosion Resistance

Qing Yang, Wenzhe Zhang, Zhengzheng Wang, Shaodong Sun

Advanced Engineering Materials· Volume 25· Issue 21
Publisher page

Abstract

To address the challenges associated with preparation of nanoporous Cu–Ni (NP‐CuNi) alloys containing high Ni concentrations, a Ni2+‐assisted dealloying strategy is proposed. The proposed strategy involves a three‐stage dealloying process primarily driven by dynamic Ni deposition/dissolution. The Ni concentration in NP‐CuNi is tuned by altering the Ni content of the Cu–Mn precursor alloy and Ni2+ in a H2SO4 solution. The Ni concentration of the nanoporous Cu66.5Ni28.5Mn5 alloy prepared in a H2SO4 + NiSO4 solution is increased by 5.2 times compared to that of the alloy prepared in the H2SO4 solution alone. Moreover, the corrosion resistance test demonstrates a reduction in corrosion current density by 58.3% compared to NP‐Cu.
Source: crossref · Quality: baseline

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.

Affiliations

Engineering Research Center of Conducting Materials and Composite Technology Ministry of Education Shaanxi Province Key Laboratory of Electrical Materials and Infiltration Technology School of Materials Science and Engineering Xi'an University of Technology Xi'an 710048 China

Funding

National Natural Science Foundation of China · Natural Science Basic Research Program of Shaanxi Province

References (31)

Show source-provided references
1. 10.1007/978-3-319-29749-110.1007/978-3-319-29749-1 ↗
2. 10.1146/annurev-matsci-070115-03173910.1146/annurev-matsci-070115-031739 ↗
3. 10.1016/j.corsci.2014.12.01710.1016/j.corsci.2014.12.017 ↗
4. 10.1002/adma.20070189910.1002/adma.200701899 ↗
5. 10.1016/j.apenergy.2020.11508810.1016/j.apenergy.2020.115088 ↗
6. 10.1038/3506852910.1038/35068529 ↗
7. 10.2320/matertrans.MT-M202001210.2320/matertrans.MT-M2020012 ↗
8. 10.1021/acs.jpcc.1c0825810.1021/acs.jpcc.1c08258 ↗
9. 10.1016/j.msea.2016.02.05510.1016/j.msea.2016.02.055 ↗
10. 10.1016/j.jallcom.2009.06.03110.1016/j.jallcom.2009.06.031 ↗
11. 10.1142/S179329201850058310.1142/S1793292018500583 ↗
12. 10.1016/j.matlet.2012.12.02810.1016/j.matlet.2012.12.028 ↗
13. 10.1016/j.corsci.2011.01.03310.1016/j.corsci.2011.01.033 ↗
14. 10.1007/s11431-013-5185-610.1007/s11431-013-5185-6 ↗
15. 10.1039/D1NR04516D10.1039/D1NR04516D ↗
16. Powell C. A. · 2000 · 00627
17. Baker H. · 1992
18. 10.1016/j.scriptamat.2014.06.03110.1016/j.scriptamat.2014.06.031 ↗
19. 10.1016/j.cej.2019.12309710.1016/j.cej.2019.123097 ↗
20. Dean J. A. · 1999
21. 10.1016/j.jpowsour.2013.08.07010.1016/j.jpowsour.2013.08.070 ↗
22. 10.1002/adfm.20150481110.1002/adfm.201504811 ↗
23. 10.1016/j.scriptamat.2018.06.02510.1016/j.scriptamat.2018.06.025 ↗
24. 10.1002/anie.20150013310.1002/anie.201500133 ↗
25. 10.1016/j.apsusc.2018.12.29010.1016/j.apsusc.2018.12.290 ↗
26. 10.1002/cnma.20200015810.1002/cnma.202000158 ↗
27. 10.1063/1.236405710.1063/1.2364057 ↗
28. 10.1088/0957-4484/23/36/36560110.1088/0957-4484/23/36/365601 ↗
29. 10.1016/S0010-938X(02)00257-310.1016/S0010-938X(02)00257-3 ↗
30. 10.1039/D0RA10678J10.1039/D0RA10678J ↗
31. 10.1149/2.0881809jes10.1149/2.0881809jes ↗