Pressure-dependent magnetization and magnetoresistivity studies on tetragonal FeS (mackinawite): revealing its intrinsic metallic character.

The transport and magnetic properties of the tetragonal Fe[Formula: see text]S were investigated using magnetoresistivity and magnetization within [Formula: see text] K, [Formula: see text] 70 kOe and [Formula: see text] 3.0 GPa. In addition, room-temperature x-ray diffraction and photoelectron spectroscopy were also applied. In contrast to previously reported nonmetallic character, Fe[Formula: see text]S is intrinsically metallic but due to a presence of a weak localization such metallic character is not exhibited below room temperature. An applied pressure reduces strongly this additional resistive contribution and as such enhances the temperature range of the metallic character which, for ∼3 GPa, is evident down to 75 K. The absence of superconductivity as well as the mechanism behind the weak localization will be discussed.

Probing the chemical and electronic properties of the core-shell architecture of transition metal trisulfide nanoribbons.

Ultraviolet and X-ray photoelectron spectroscopies are used to probe the chemical and electronic structure of an amorphous, 2-20 nm-thick shell that encases the crystalline core in core-shell nanoribbons of TaS(3). The shell is chemically heterogeneous, containing elemental sulfur and a with a notable (S(2))(2-) deficiency over the crystalline TaS(3) core. We find nanoribbon stability to be substrate-dependent; whilst the ribbons are stable on the native oxide of a silicon surface, mass transport of sulfur species between the amorphous shell and a gold substrate leads to a significant change in the electronic properties of the nanomaterials. Our observations may have general implications for the incorporation of nanostructured transition metal chalcogenides into electronic devices.