Covalent Bonding-Based Adhesion Method for Rigidly Coupling Metal Nanocrystals to Metal and Metal Oxide Surfaces
Source abstract
Abstract
The major challenges of developing a robust strain coupling between nanocrystals and a strain medium are addressed by employing a simple self-assembly-based adhesion process that relies on the formation of metal-oxide bonds between Ni nanocrystals and various surfaces. X-ray photoelectron spectroscopy indicates that the adhesion mechanism necessitates high oxidation potential surfaces capable of metal-oxide bond formation. The process is demonstrated to be reversible, using a reducing plasma to induce adhesion in previously unadhered NiO/Ni nanocrystals. Adhesion to the substrate develops interfacial stress in the nanocrystals resulting in a 40 Oe increase in coercivity and a 25 K shift in the blocking temperature.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Nanofabrication and Lithography Techniques · Molecular Junctions and Nanostructures · Quantum Dots Synthesis And Properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry and Biochemistry, UCLA, Los Angeles, California 90095, United States
Department of Materials Science and Engineering, UCLA, Los Angeles, California 90095, United States
California NanoSystems Institute, University of California, Los Angeles, California 90095, United States
Funding
Office of Integrative Activities · Division of Engineering Education and Centers
References (47)
Show source-provided references
1. 10.1002/ange.20046166510.1002/ange.200461665 ↗
2. 10.1002/anie.20080224810.1002/anie.200802248 ↗
3. 10.1166/jnn.2009.j05610.1166/jnn.2009.j056 ↗
4. 10.1021/nl063039w10.1021/nl063039w ↗
5. 10.1063/1.300598510.1063/1.3005985 ↗
6. 10.1016/j.mseb.2009.02.00610.1016/j.mseb.2009.02.006 ↗
7. 10.1016/j.apsusc.2014.07.20310.1016/j.apsusc.2014.07.203 ↗
8. 10.1126/science.111054910.1126/science.1110549 ↗
9. 10.1038/nnano.2015.2410.1038/nnano.2015.24 ↗
10. 10.1109/tnano.2015.246233710.1109/tnano.2015.2462337 ↗
11. 10.1038/nmat331110.1038/nmat3311 ↗
12. 10.1038/s41565-018-0339-010.1038/s41565-018-0339-0 ↗
13. 10.1038/ncomms156410.1038/ncomms1564 ↗
14. 10.1063/1.496167010.1063/1.4961670 ↗
15. 10.1063/1.337359310.1063/1.3373593 ↗
16. 10.1063/1.496095210.1063/1.4960952 ↗
17. Spaldin N. A. · 201010.1017/CBO9780511781599 ↗
18. 10.1021/nl303463710.1021/nl3034637 ↗
19. 10.1088/0957-4484/25/5/05570210.1088/0957-4484/25/5/055702 ↗
20. 10.1016/j.jmmm.2018.05.06110.1016/j.jmmm.2018.05.061 ↗
21. 10.1021/cm400047610.1021/cm4000476 ↗
22. 10.1002/chem.20120107110.1002/chem.201201071 ↗
23. 10.1038/nmat452610.1038/nmat4526 ↗
24. 10.3390/nano810081010.3390/nano8100810 ↗
25. 10.1088/0953-8984/27/50/50400110.1088/0953-8984/27/50/504001 ↗
26. 10.1038/nmat387010.1038/nmat3870 ↗
27. 10.1002/adma.20080162010.1002/adma.200801620 ↗
28. 10.1002/anie.20110599610.1002/anie.201105996 ↗
29. 10.1002/adfm.20080027410.1002/adfm.200800274 ↗
30. 10.1002/anie.20191113510.1002/anie.201911135 ↗
31. 10.1016/j.jmmm.2016.05.06410.1016/j.jmmm.2016.05.064 ↗
32. 10.1063/1.216659710.1063/1.2166597 ↗
33. 10.1103/physrevb.82.04511710.1103/physrevb.82.045117 ↗
34. 10.1186/1556-276x-7-52810.1186/1556-276x-7-528 ↗
35. 10.1088/0957-4484/24/25/25570110.1088/0957-4484/24/25/255701 ↗
36. 10.1021/acs.nanolett.9b0295610.1021/acs.nanolett.9b02956 ↗
37. 10.1021/cm902007g10.1021/cm902007g ↗
38. 10.1088/0268-1242/8/7/03710.1088/0268-1242/8/7/037 ↗
39. 10.1016/j.apsusc.2005.06.00410.1016/j.apsusc.2005.06.004 ↗
40. 10.1088/0957-4484/18/11/11561310.1088/0957-4484/18/11/115613 ↗
41. 10.1016/s0167-5729(02)00100-010.1016/s0167-5729(02)00100-0 ↗
42. 10.1063/1.242444410.1063/1.2424444 ↗
43. 10.1063/1.12672710.1063/1.126727 ↗
44. 10.1021/nn900019x10.1021/nn900019x ↗
45. 10.1063/1.486619610.1063/1.4866196 ↗
46. 10.1021/nl301642g10.1021/nl301642g ↗
47. 10.1021/acs.chemmater.0c0175810.1021/acs.chemmater.0c01758 ↗