Tailoring the Strength of Nanoporous Gold by Self-Assembled Monolayers of Alkanethiols
Source abstract
Abstract
Because of the large specific surface area, the properties of nanoporous metals and in particular their mechanical properties are sensitive to chemical modifications of their surfaces. Here, we exploit self-assembled monolayers (SAMs) to modify a surface of nanoporous gold and study their effect on plastic behavior. The SAMs investigated here (i) are made from alkanethiols, which consist of a sulfur headgroup that strongly binds to metal substrates, a hydrocarbon chain, and an end group, and (ii) are known to spontaneously self-organize into well-ordered, dense two-dimensional molecular films on the surface of coinage metals. Alkanethiols with various chain lengths and terminal groups were used to prepare SAMs on bulk nanoporous gold, and compression tests were performed on the SAM-modified and nonmodified macroscopic samples. Our experiments reveal a substantial, up to 50%, increase of the flow stress due to thiol adsorption. We attribute the strengthening to the adsorption locking of dislocation end points at the surface, which is mediated by the fairly strong metal–sulfur interaction.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Nanoporous metals and alloys · Electrocatalysts for Energy Conversion · Nanocluster Synthesis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Institute of Materials Research, Materials Mechanics, Helmholtz-Zentrum Geesthacht, 21502 Geesthacht, Germany
Institute of Materials Physics and Technology, Hamburg University of Technology, 21073 Hamburg, Germany
Institute of Functional Interfaces, Karlsruhe Institute of Technology, 76344 Eggenstein-Leopoldshafen, Germany
Funding
Deutsche Forschungsgemeinschaft
References (59)
Show source-provided references
1. 10.1080/21663831.2015.109467910.1080/21663831.2015.1094679 ↗
2. 10.1063/1.243671810.1063/1.2436718 ↗
3. 10.1557/mrs.2017.30210.1557/mrs.2017.302 ↗
4. Biener J. · 2008 · 11810.1007/978-0-387-78701-5_6 ↗
5. 10.1016/j.scriptamat.2015.08.00210.1016/j.scriptamat.2015.08.002 ↗
6. 10.1021/nl048999210.1021/nl0489992 ↗
7. 10.1016/j.actamat.2005.10.00810.1016/j.actamat.2005.10.008 ↗
8. 10.1016/j.actamat.2013.02.01310.1016/j.actamat.2013.02.013 ↗
9. 10.1021/acs.nanolett.7b0295010.1021/acs.nanolett.7b02950 ↗
10. 10.1126/science.120219010.1126/science.1202190 ↗
11. 10.1016/j.actamat.2014.04.06710.1016/j.actamat.2014.04.067 ↗
12. 10.1063/1.483168610.1063/1.4831686 ↗
13. 10.1038/nmat433510.1038/nmat4335 ↗
14. 10.1088/0953-8984/16/28/R0110.1088/0953-8984/16/28/R01 ↗
15. 10.1021/cr030078910.1021/cr0300789 ↗
16. 10.1016/j.progsurf.2009.06.00110.1016/j.progsurf.2009.06.001 ↗
17. 10.1039/b907301a10.1039/b907301a ↗
18. 10.1016/j.progsurf.2010.05.00110.1016/j.progsurf.2010.05.001 ↗
19. 10.1002/chem.1996002031810.1002/chem.19960020318 ↗
20. 10.1021/ja963571t10.1021/ja963571t ↗
21. 10.5012/bkcs.2010.31.11.340710.5012/bkcs.2010.31.11.3407 ↗
22. 10.1039/c0cp02553d10.1039/c0cp02553d ↗
23. 10.1021/acs.jpcc.6b0580210.1021/acs.jpcc.6b05802 ↗
24. 10.1016/j.apsusc.2016.07.05910.1016/j.apsusc.2016.07.059 ↗
25. 10.1063/1.497278010.1063/1.4972780 ↗
26. 10.1016/j.jelechem.2016.10.01310.1016/j.jelechem.2016.10.013 ↗
27. 10.1016/j.apsusc.2016.05.14910.1016/j.apsusc.2016.05.149 ↗
28. 10.1016/S0079-6816(00)00024-110.1016/S0079-6816(00)00024-1 ↗
29. 10.1088/0953-8984/20/18/18400410.1088/0953-8984/20/18/184004 ↗
30. 10.1021/la804251a10.1021/la804251a ↗
31. 10.1080/21663831.2016.127648510.1080/21663831.2016.1276485 ↗
32. 10.1021/jp063521310.1021/jp0635213 ↗
33. 10.1126/science.276.5321.202110.1126/science.276.5321.2021 ↗
34. 10.1021/la030257l10.1021/la030257l ↗
35. 10.1021/la062441n10.1021/la062441n ↗
36. 10.1088/0957-4484/21/7/07550110.1088/0957-4484/21/7/075501 ↗
37. 10.1038/nmat312410.1038/nmat3124 ↗
38. 10.1016/j.actamat.2014.01.01310.1016/j.actamat.2014.01.013 ↗
39. 10.1038/s41467-017-01434-210.1038/s41467-017-01434-2 ↗
40. 10.1016/j.actamat.2015.04.02110.1016/j.actamat.2015.04.021 ↗
41. 10.1016/j.actamat.2009.02.01710.1016/j.actamat.2009.02.017 ↗
42. 10.1021/ja00183a04910.1021/ja00183a049 ↗
43. 10.1002/adfm.20160093810.1002/adfm.201600938 ↗
44. 10.1016/0022-0728(91)85271-P10.1016/0022-0728(91)85271-P ↗
45. 10.1016/j.colsurfa.2011.09.02010.1016/j.colsurfa.2011.09.020 ↗
46. 10.1038/nchem.135210.1038/nchem.1352 ↗
47. 10.1021/la960777z10.1021/la960777z ↗
48. Latanision R. M. · 197710.1007/978-94-011-9691-8 ↗
49. 10.1088/0034-4885/64/5/20110.1088/0034-4885/64/5/201 ↗
50. 10.1016/S1359-6454(96)00314-X10.1016/S1359-6454(96)00314-X ↗
51. 10.1016/0040-6090(95)06995-X10.1016/0040-6090(95)06995-X ↗
52. 10.1103/PhysRevB.82.04140810.1103/PhysRevB.82.041408 ↗
53. 10.1080/1478643620821262910.1080/14786436208212629 ↗
54. Jerkiewicz, G. In Interfacial Electrochemistry: Theory: Experiment, and Applications; Wieckowski, A., Ed. Marcel Dekker: 1999; Chapter 32, pp 559–576.
55. 10.1016/j.scriptamat.2006.09.01610.1016/j.scriptamat.2006.09.016 ↗
56. 10.1021/ja00040a05810.1021/ja00040a058 ↗
57. 10.1126/science.108102410.1126/science.1081024 ↗
58. 10.1038/ncomms523710.1038/ncomms5237 ↗
59. 10.1021/la00001a00510.1021/la00001a005 ↗