Vicky V. T. Doan-Nguyen, Simon A. J. Kimber, Diego Pontoni, Benjamin T. Diroll, Danielle C. Reifsnyder, Marcel Miglierini, Xiaohao Yang, Christopher B. Murray, Simon J. L. Billinge
We demonstrate a remarkable equivalence in structure measured by total X-ray scattering methods between very small metallic nanoparticles and bulk metallic glasses (BMGs), thus connecting two disparate fields, shedding new light on both. Our results show that for nanoparticle diameters <5 nm the structure of Ni nanoparticles changes from fcc to the characteristic BMG-like structure, despite them being formed from a single element, an effect we call nano-metallic glass (NMG) formation. However, high-resolution TEM images of the NMG clusters exhibit lattice fringes indicating a locally well-ordered, rather than glassy, structure. These seemingly contradictory results may be reconciled by finding a locally ordered structure that is highly isotropic and we show that local icosahedral packing within 5 atomic shells explains this. Since this structure is stabilized only in the vicinity of a surface suggests which highlights the importance of the presence of free volume in BMGs for stabilizing similar local clusters.
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http://arxiv.org/abs/1305.7261
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