Matti Alatalo

X-ray Compton scattering experiments along with parallel first-principles computations were carried out on LiNiO2 to understand the effects of W doping on this cathode material for Li-ion batteries. By employing high-energy x rays exceeding 100 keV, an insight is gained into the fate of the W valence electrons, which are adduced to undergo transfer to empty O 2p energy bands within the active oxide matrix of the cathode. The substitution of W for Ni is shown to increase the electronic conductivity and to enhance the total magnetization per Ni atom. Our study demonstrates that an analysis of line shapes of Compton scattered x rays in combination with theoretical modeling can provide a precise method for an atomic level understanding of the nature of the doping process.

The presence of a long‐abandoned hexagonal omega (ω) phase in steel samples is recently gaining momentum owing to the advances in transmission electron microscopy (TEM) measurements, even though it is already reported in other transition‐metal alloys. The stabilization of this metastable phase is mainly investigated in presence of C, even though the formation of the ω phase is attributed to the combined effect of many factors, one among which is the enrichment of solute elements such as Al, Mn, Si, C, and Cr in the nanometer‐sized regimes. The present study investigates the effect of the above alloying elements in ω‐Fe using density functional theory (DFT) calculations. It is seen that the magnetic states of the atoms play a major role in the stability of ω‐Fe. Cohesive energy calculations show that the alloying elements affect the energetics and stabilization of ω‐Fe. Further, density of states calculations reveal the variation in d‐band occupancy in the presence of alloying elements, which in turn affects the cohesive energy. Phonon band structure calculations show that only ω‐Fe with substitutional C shows positive frequencies and hence possess thermodynamic stability. Finally, we confirm the existence of ω‐Fe using TEM measurements of a steel sample containing the same alloying elements. Our results can shed light on the stabilization of the ω in other transition‐metal alloys as well, in the presence of minor alloying elements.

We have performed a density functional theory study of the MoS₂ monolayer and the MoS₂ (100) and (103) surfaces in relation to the early stages of the hydrodesulfurization reaction. In many X-ray diffraction (XRD) results, the (103) surface exhibits a higher peak than the (100) surface, yet one of the most frequently occurring surface has not been studied extensively. By analyzing experimental studies, we conclude that the (103) surface of MoS₂ is the most frequently occurring edge surface when the sample size is thicker than ∼10–15 nm. Herein, we report the first comparison of reaction paths for the formation of a sulfur vacancy on the (103) surface of MoS₂, monolayer, and (100) surface of MoS₂. The reason for the occurence of the (103) surface in the XRD patterns has been established. We point out the similarity in the reaction barriers for the monolayer and (100) and (103) surfaces and discuss the reason for it. Moreover, we found a more energetically favorable step in the reaction pathway for the formation of a sulfur vacancy, which allowed us to refine the previously established pathway.

A critical factor for electronics based on inorganic layered crystals stems from the electrical contact mode between the semiconducting crystals and the metal counterparts in the electric circuit. Here, a materials tailoring strategy via nanocomposite decoration is carried out to reach metallic contact between MoS₂ matrix and transition metal nanoparticles. Nickel nanoparticles (NiNPs) are successfully joined to the sides of a layered MoS₂ crystal through gold nanobuffers, forming semiconducting and magnetic NiNPs@MoS₂ complexes. The intrinsic semiconducting property of MoS₂ remains unchanged, and it can be lowered to only few layers. Chemical bonding of the Ni to the MoS₂ host is verified by synchrotron radiation based photoemission electron microscopy, and further proved by first‐principles calculations. Following the system's band alignment, new electron migration channels between metal and the semiconducting side contribute to the metallic contact mechanism, while semiconductor–metal heterojunctions enhance the photocatalytic ability.