Impact of host phonons on interstitial diffusion.

The net effect of host phonons on interstitial diffusion has remained as a fundamental knowledge gap in our current theories since the motions of the host atoms and interstitials were coupled in these theories. Here we study this effect through molecular dynamics simulations of hydrogen diffusion in palladium, in which the motions can be decoupled through pinning the host atoms. Mathematically this decoupling corresponds to expanding the total diffusion coefficient into a Taylor series, which separates the phonon contribution from the intrinsic interstitial jumping.

Large-scale stationary hydrogen storage via liquid organic hydrogen carriers.

Large-scale stationary hydrogen storage is critical if hydrogen is to fulfill its promise as a global energy carrier. While densified storage via compressed gas and liquid hydrogen is currently the dominant approach, liquid organic molecules have emerged as a favorable storage medium because of their desirable properties, such as low cost and compatibility with existing fuel transport infrastructure. This perspective article analytically investigates hydrogenation systems' technical and economic prospects using liquid organic hydrogen carriers (LOHCs) to store hydrogen at a large scale compared to densified storage technologies and circular hydrogen carriers (mainly ammonia and methanol).

Chiral metallic glass nanolattices with combined lower density and improved auxeticity.

Auxetic materials are promising structural and functional candidates due to their unique lateral expansion when stretched, however, bulk metallic glasses (MGs) could not show any auxeticity because of their intrinsic isotropic nature. Here we construct chiral CuZr metallic glass nanolattices with cavities, and investigate their auxeticity and underlying mechanism with molecular dynamics simulations. It is found that, compared to monolithic MGs, all the chiral metallic glass nanolattices (CMGNs) exhibit improved auxeticity and lower density.

Atomic-level crystallization in selective laser melting fabricated Zr-based metallic glasses.

As a promising additive manufacturing technique, selective laser melting (SLM) provides the possibility of fabricating metallic glassy components free of the constraints of geometrical complexity and dimensions. However, unexpected crystallization greatly affects the microstructure and degrades the mechanical performance of SLM-fabricated metallic glasses (MGs). To clarify the crystallization mechanism and the effect of laser processing on the crystallization, we investigate the atomic-level crystallization in the SLM ZrCu MG by using molecular dynamics simulations.

Composition susceptibility and the role of one, two, and three-body interactions in glass forming alloys: CuZr vs NiAl.

In this paper, we compare the composition fluctuations and interaction potentials of a good metallic glass former, CuZr, and a poor glass former, NiAl. The Bhatia-Thornton correlation functions are calculated. Motivated by the observation of chemical ordering at the NiAl surface, we derive a new property, R^(q), corresponding to the linear susceptibility of concentration to a perturbation in density.

Chemical ordering and crystal nucleation at the liquid surface: A comparison of CuZr and NiAl alloys.

We study the influence of the liquid-vapor surface on the crystallization kinetics of supercooled metal alloys. While a good glass former, CuZr, shows no evidence of surface enhancement of crystallization, NiAl exhibits an increased rate of crystallization due to heterogeneous nucleation at the free liquid surface. The difference in the compositional fluctuations at the interface is proposed as the explanation of the distinction between the two alloys.

A priori calculations of the free energy of formation from solution of polymorphic self-assembled monolayers.

Modern quantum chemical electronic structure methods typically applied to localized chemical bonding are developed to predict atomic structures and free energies for meso-tetraalkylporphyrin self-assembled monolayer (SAM) polymorph formation from organic solution on highly ordered pyrolytic graphite surfaces. Large polymorph-dependent dispersion-induced substrate-molecule interactions (e.g.

Catalytic potential of highly defective (211) surfaces of zinc blende ZnO.

Zinc blende (ZB) ZnO has gained increasing research interest due to its favorable properties and its stabilization on the nanoscale. While surface properties are important on the nanoscale, the studies on ZB ZnO surface properties are rare. Here we have performed first principles calculations of the energies and structures of ZB and wurtzite (WZ) ZnO surfaces.

Intermixed adatom and surface-bound adsorbates in regular self-assembled monolayers of racemic 2-butanethiol on Au(111).

In situ scanning tunneling microscopy combined with density functional theory molecular dynamics simulations reveal a complex structure for the self-assembled monolayer (SAM) of racemic 2-butanethiol on Au(111) in aqueous solution. Six adsorbate molecules occupy a (10×√3)R30° cell organized as two RSAuSR adatom-bound motifs plus two RS species bound directly to face-centered-cubic and hexagonally close-packed sites. This is the first time that these competing head-group arrangements have been observed in the same ordered SAM.

Controlling the stereochemistry and regularity of butanethiol self-assembled monolayers on au(111).

The rich stereochemistry of the self-assembled monolayers (SAMs) of four butanethiols on Au(111) is described, the SAMs containing up to 12 individual C, S, or Au chiral centers per surface unit cell. This is facilitated by synthesis of enantiomerically pure 2-butanethiol (the smallest unsubstituted chiral alkanethiol), followed by in situ scanning tunneling microscopy (STM) imaging combined with density functional theory molecular dynamics STM image simulations. Even though butanethiol SAMs manifest strong headgroup interactions, steric interactions are shown to dominate SAM structure and chirality.

Activity of ZnO polar surfaces: an insight from surface energies.

The calculation of the accurate surface energies for (0001) surfaces of wurtzite ZnO is difficult because it is impossible to decouple the two inequivalent (0001)-Zn and (0001¯)-O surfaces. By using a heterojunction model we have transformed the uncertainty of the surface energies into that of interface energies which is much smaller than the former and hence estimated the surface energies to a high degree of accuracy. It is found that the oxygen terminated (0001¯)-O face of the wurtzite phase and (1¯1¯1¯O of the zinc blende phase are more stable than their Zn-terminated counterparts within the major temperature and oxygen partial pressure range accessible to experiment.

Anomalously slow crystal growth of the glass-forming alloy CuZr.

Our ability to exploit the benefits of metallic glasses depends on identifying alloys of high glass-forming ability (GFA). So far, the established empirical correlations of GFA (ref. ) are statistical guides at best and lack a microscopic rationale.