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Register a new userSurface energy of strained amorphous solids
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Added by
Kari Dalnoki-Veress
Publication date
2017
fields
Physics
and research's language is
English
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Surface stress and surface energy are fundamental quantities which characterize the interface between two materials. Although these quantities are identical for interfaces involving only fluids, the Shuttleworth effect demonstrates that this is not the case for most interfaces involving solids, since their surface energies change with strain. Crystalline materials are known to have strain dependent surface energies, but in amorphous materials, such as polymeric glasses and elastomers, the strain dependence is debated due to a dearth of direct measurements. Here, we utilize contact angle measurements on strained glassy and elastomeric solids to address this matter. We show conclusively that interfaces involving polymeric glasses exhibit strain dependent surface energies, and give strong evidence for the absence of such a dependence for incompressible elastomers. The results provide fundamental insight into our understanding of the interfaces of amorphous solids and their interaction with contacting liquids.
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It is known by now that amorphous solids at zero temperature do not possess a nonlinear elasticity theory: besides the shear modulus which exists, all the higher order coefficients do not exist in the thermodynamic limit. Here we show that the same phenomenon persists up to temperatures comparable to the glass transition. The zero temperature mechanism due to the prevalence of dangerous plastic modes of the Hessian matrix is replaced by anomalous stress fluctuations that lead to the divergence of the variances of the higher order elastic coefficients. The conclusion is that in amorphous solids elasticity can never be decoupled from plasticity: the nonlinear response is very substantially plastic.
We discuss memory effects in the conductance of hopping insulators due to slow rearrangements of structural defects leading to formation of polarons close to the electron hopping states. An abrupt change in the gate voltage and corresponding shift of the chemical potential change populations of the hopping sites, which then slowly relax due to rearrangements of structural defects. As a result, the density of hopping states becomes time dependent on a scale relevant to rearrangement of the structural defects leading to the excess time dependent conductivity.
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Majorana quasiparticles (MQPs) in condensed matter play an important role in strategies for topological quantum computing but still remain elusive. Vortex cores of topological superconductors may accommodate MQPs that appear as the zero-energy vortex bound state (ZVBS). An iron-based superconductor Fe(Se,Te) possesses a superconducting topological surface state that has been investigated by scanning tunneling microscopies to detect the ZVBS. However, the results are still controversial. Here, we performed spectroscopic-imaging scanning tunneling microscopy with unprecedentedly high energy resolution to clarify the nature of the vortex bound states in Fe(Se,Te). We found the ZVBS at 0 $pm$ 20 $mu$eV suggesting its MQP origin, and revealed that some vortices host the ZVBS while others do not. The fraction of vortices hosting the ZVBS decreases with increasing magnetic field, while chemical and electronic quenched disorders are apparently unrelated to the ZVBS. These observations elucidate the conditions to achieve the ZVBS, and may lead to controlling MQPs.
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