Hardening in Au-Ag nanoboxes from stacking fault-dislocation interactions.
Radhika P PatilDavid DoanZachary H AitkenShuai ChenMehrdad T KianiChristopher M BarrKhalid HattarYong-Wei ZhangX Wendy GuPublished in: Nature communications (2020)
Porous, nano-architected metals with dimensions down to ~10 nm are predicted to have extraordinarily high strength and stiffness per weight, but have been challenging to fabricate and test experimentally. Here, we use colloidal synthesis to make ~140 nm length and ~15 nm wall thickness hollow Au-Ag nanoboxes with smooth and rough surfaces. In situ scanning electron microscope and transmission electron microscope testing of the smooth and rough nanoboxes show them to yield at 130 ± 45 MPa and 96 ± 31 MPa respectively, with significant strain hardening. A higher strain hardening rate is seen in rough nanoboxes than smooth nanoboxes. Finite element modeling is used to show that the structure of the nanoboxes is not responsible for the hardening behavior suggesting that material mechanisms are the source of observed hardening. Molecular dynamics simulations indicate that hardening is a result of interactions between dislocations and the associated increase in dislocation density.
Keyphrases
- molecular dynamics simulations
- photodynamic therapy
- finite element
- quantum dots
- highly efficient
- sensitive detection
- electron microscopy
- molecular docking
- visible light
- physical activity
- high resolution
- optical coherence tomography
- human health
- weight loss
- mass spectrometry
- pseudomonas aeruginosa
- light emitting
- electron transfer
- metal organic framework
- solar cells
- simultaneous determination