New Insights into the All-Dry Synthesis of NMC622 Cathodes Using a Single-Phase Rock Salt Oxide Precursor.

In this study, new insights into the all-dry synthesis of the LiNi0.6Mn0.2Co0.2O2 (NMC622) cathode using a single-phase rock-salt (RS) oxide precursor are provided. It was found that use of a larger amount of excess Li content not only can enhance the electrochemical performance of NMC made from the RS-precursor but also increase the degree of homogeneity of the NMC cathode material. In situ XRD analysis showed that lithiation of the RS-precursor (i.e., formation of the O3-phase) starts at a higher synthesis temperature (∼450 °C) than that is required when using a hydroxide precursor (HP) and lithium carbonate (∼350 °C). Consequently, Li2CO3 was consumed by the reaction with the HP at low temperatures before the temperature reached the Li2CO3 melting point. In contrast, the reduced lithiation kinetics of the RS-precursor results in the presence of liquid Li2CO3 during the synthesis, which rapidly increases the rates of precursor lithiation and increases the NMC primary particle size.

Voronoi-Tessellated Graphite Produced by Low-Temperature Catalytic Graphitization from Renewable Resources.

A highly crystalline graphite powder was prepared from the low temperature (800-1000 °C) graphitization of renewable hard carbon precursors using a magnesium catalyst. The resulting graphite particles are composed of Voronoi-tessellated regions comprising irregular sheets; each Voronoi-tessellated region having a small "seed" particle located near their centroid on the surface. This suggests nucleated outward growth of graphitic carbon, which has not been previously observed. Each seed particle consists of a spheroidal graphite shell on the inside of which hexagonal graphite platelets are perpendicularly affixed. This results in a unique high surface area graphite with a high degree of graphitization that is made with renewable feedstocks at temperatures far below that conventionally used for artificial graphites.

Ca6[Cr2N6]H, the first quaternary nitride-hydride.

The novel quaternary nitride-hydride Ca(6)[Cr(2)N(6)]H was synthesized at 1000 degrees C in sealed niobium or stainless steel tubes. It crystallizes in the space group R3 (No. 148, Z = 3) with lattice constants (A) a = 9.0042(2) and c = 9.1898(3) and contains the complex anion [Cr(2)N(6)](11)(-) with a short chromium-chromium bond length of 2.26 A. To our knowledge, this is the first example of a non-nitrogen-bridged chromium-chromium dimer in an extended structure compound. Magnetic susceptibility measurements reveal the compound to be paramagnetic at room temperature and with a broad antiferromagnetic ordering centered around 55 K.