Synthesis of Atomically Thin Hexagonal Diamond with Compression.

Atomically thin diamond, also called diamane, is a two-dimensional carbon allotrope and has attracted considerable scientific interest because of its potential physical properties. However, the successful synthesis of a pristine diamane has up until now not been achieved. We demonstrate the realization of a pristine diamane through diamondization of mechanically exfoliated few-layer graphene via compression. Resistance, optical absorption, and X-ray diffraction measurements reveal that hexagonal diamane (h-diamane) with a bandgap of 2.8 ± 0.3 eV forms by compressing trilayer and thicker graphene to above 20 GPa at room temperature and can be preserved upon decompression to ∼1.0 GPa. Theoretical calculations indicate that a (-2110)-oriented h-diamane is energetically stable and has a lower enthalpy than its few-layer graphene precursor above the transition pressure. Compared to gapless graphene, semiconducting h-diamane offers exciting possibilities for carbon-based electronic devices.

Reversal in the Size Dependence of Grain Rotation.

The conventional belief, based on the Read-Shockley model for the grain rotation mechanism, has been that smaller grains rotate more under stress due to the motion of grain boundary dislocations. However, in our high-pressure synchrotron Laue x-ray microdiffraction experiments, 70 nm nickel particles are found to rotate more than any other grain size. We infer that the reversal in the size dependence of the grain rotation arises from the crossover between the grain boundary dislocation-mediated and grain interior dislocation-mediated deformation mechanisms. The dislocation activities in the grain interiors are evidenced by the deformation texture of nickel nanocrystals. This new finding reshapes our view on the mechanism of grain rotation and helps us to better understand the plastic deformation of nanomaterials, particularly of the competing effects of grain boundary and grain interior dislocations.

Pressure-induced enhancement in the superconductivity of ZrTe3.

We report the superconductivity enhancement of ZrTe3 on compression up to 33 GPa. The superconducting transition occurs above 4.1 GPa and the superconducting temperature (T C) increases with pressure in further compression, reaching a maximum of 7.1 K at ~28 GPa. An anomalous change of superconducting temperature is seen in the compression above 21 GPa. No structural phase transition is observed in the whole compression up to 36 GPa, but a subtle change in structural parameter is seen between 17-19 GPa, which seems relevant to the anomalous increase in the superconducting temperature. First-principle calculations reveal that the density of states at the Fermi level increases with pressure, which explains the enhancement of T C in ZrTe3 under compression.