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Register a new userBulk metallic glass-like structure of small icosahedral metallic nanoparticles
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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 which highlights the importance of the presence of free volume in BMGs for stabilizing similar local clusters.
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The glass transition remains unclarified in condensed matter physics. Investigating the mechanical properties of glass is challenging because any global deformation that may result in shear rejuvenation requires an astronomical relaxation time. Moreover, it is well known that a glass is heterogeneous and a global perturbation cannot explore local mechanical/transport properties. However, an investigation based on a local probe, i.e. microrheology, may overcome these problems. Here, we establish active microrheology of a bulk metallic glass: a probe particle driven into host medium glass. This is a technique amenable for experimental investigations. We show that upon cooling the microscopic friction exhibits a second-order phase transition; this sheds light on the origin of friction in heterogeneous materials. Further, we provide distinct evidence to demonstrate that a strong relationship exists between the microscopic dynamics of the probe particle and the macroscopic properties of the host medium glass. These findings establish active microrheology as a promising technique for investigating the local properties of bulk metallic glass.
Physically vitrifying single-element metallic glass requires ultrahigh cooling rates, which are still unachievable for most of the closest-packed metals. Here, we report a facile synthetic strategy for creating mono-atomic palladium metallic glass nanoparticles with a purity of 99.35 +/- 0.23 at% from palladium-silicon liquid droplets using a cooling rate below 1000 K/s. In-situ environmental transmission electron microscopy directly detected the leaching of silicon. Further hydrogen absorption experiment showed that this palladium metallic glass expanded little upon hydrogen uptake, exhibiting a great potential application for hydrogen separation. Our results provide insight into the formation of mono-atomic metallic glass at nanoscale.
Scanning tunneling microscopy (STM) observations resolve the structure and dynamics of metallic glass Cu$_{100-x}$Hf$_{x}$ films and demonstrate STM control of aging at a metallic glass surface. Surface clusters exhibit heterogeneous hopping dynamics. Low Hf concentration films feature an aged surface of larger, slower clusters. Argon ion-sputtering destroys the aged configuration, yielding a surface in constant fluctuation. STM can locally restore the relaxed state, allowing for nanoscale lithographic definition of aged sections.
Micro- and nano-resonators have important applications including sensing, navigation, and biochemical detection. Their performance is quantified using the quality factor $Q$, which gives the ratio of the energy stored to the energy dissipated per cycle. Metallic glasses are a promising materials class for micro- and nano-scale resonators since they are amorphous and can be fabricated precisely into complex shapes on these lengthscales. To understand the intrinsic dissipation mechanisms that ultimately limit large $Q$-values in metallic glasses, we perform molecular dynamics simulations to model metallic glass resonators subjected to bending vibrations. We calculate the vibrational density of states, redistribution of energy from the fundamental mode of vibration, and $Q$ versus the kinetic energy per atom $K$ of the excitation. In the linear and nonlinear response regimes where there are no atomic rearrangements, we find that $Q rightarrow infty$ (since we do not consider coupling to the environment). We identify a characteristic $K_r$ above which atomic rearrangements occur, and there is significant energy leakage from the fundamental mode to higher frequencies, causing finite $Q$. Thus, $K_r$ is a critical parameter determining resonator performance. We show that $K_r$ decreases as a power-law, $K_rsim N^{-k},$ with increasing system size $N$, where $k approx 1.3$. We estimate the critical strain $langle gamma_r rangle sim 10^{-8}$ for micron-sized resonators below which atomic rearrangements do not occur, and thus large $Q$-values can be obtained when they are operated below $gamma_r$. We find that $K_r$ for amorphous resonators is comparable to that for resonators with crystalline order.
The magnetic behavior of $Fe_{3-x}O_4$ nanoparticles synthesized either by high-temperature decomposition of an organic iron precursor or low-temperature co-precipitation in aqueous conditions, is compared. Transmission electron microscopy, X-ray absorption spectroscopy, X-ray magnetic circular dichroism and magnetization measurements show that nanoparticles synthesized by thermal decomposition display high crystal quality and bulk-like magnetic and electronic properties, while nanoparticles synthesized by co-precipitation show much poorer crystallinity and particle-like phenomenology, including reduced magnetization, high closure fields and shifted hysteresis loops. The key role of the crystal quality is thus suggested since particle-like behavior for particles larger than about 5 nm is only observed when they are structurally defective. These conclusions are supported by Monte Carlo simulations. It is also shown that thermal decomposition is capable of producing nanoparticles that, after further stabilization in physiological conditions, are suitable for biomedical applications such as magnetic resonance imaging or bio-distribution studies.
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