Qiankun Zhang

Ni3C-assisted growth of carbon nanofibres 300 °c by thermal CVD

Ni-assisted thermal chemical vapor deposition (TCVD) is one of the most common techniques for the growth of carbon nanofibres/nanotubes (CNFs/CNTs). However, some fundamental issues related to the catalytic growth of CNFs/CNTs, such as the low-limit growth temperature, the limiting steps and the state of Ni, are still controversial. Here, we report the growth of CNFs at 300 °C; that is the lowest temperature for the growth of CNFs by TCVD using Ni as the catalyst so far. The results showed that the Ni existed in rhombohedral Ni3C, not in the normal form of face-centered cubic Ni, and the C atoms for building the CNFs were precipitated from the (001) planes of the faceted Ni3C nanoparticles. The CNFs are believed to be formed by the decomposition-formation cycle of metastable Ni3C that has a low-limit decomposition temperature of about 300 °C. Our results strongly suggest that TCVD is a valuable tool for the synthesis of CNFs/CNTs at temperatures below 400 °C, which is generally considered as the upper-limit temperature for fabricating complementary metal oxide semiconductor devices but is the low-limit temperature for growing CNFs/CNTs by TCVD at present.

Synthesis and magnetic properties of Fe3C-C core-shell nanoparticles.

Fe3C-C core-shell nanoparticles were fabricated on a large scale by metal-organic chemical vapor deposition at 700 °C with ferric acetylacetonate as the precursor. Analysis results of x-ray diffraction, transmission electron microscope and Raman spectroscope showed that the Fe3C cores with an average diameter of ∼35 nm were capsulated by the graphite-like C layers with the thickness of 2-5 nm. The comparative experiments revealed that considerable Fe3O4-Fe3C core-shell nanoparticles and C nanotubes were generated simultaneously at 600 and 800 °C, respectively. A formation mechanism was proposed for the as-synthesized core-shell nanostructures, based on the temperature-dependent catalytic activity of Fe3C nanoclusters and the coalescence process of Fe3C-C nanoclusters. The Fe3C-C core-shell nanoparticles exhibited a saturation magnetization of 23.6 emu g(-1) and a coercivity of 550 Oe at room temperature.

In situ synthesis and strengthening of powder metallurgy high speed steel in addition of LaB 6

A novel technology which was characterized by the vacuum solid state sintering was developed for powder metallurgy high speed steels production. During sintering, both the WC and Mo2C reacted with Fe and transformed to W and Mo rich M6C carbides which were the common hard phases in high speed steels. Also, a high number of W, Mo and Fe were dissolved in VC, forming the MC carbides. The densification of the material mainly relied on the solubility effect during the M6C and MC carbides formation. By alloying with a 0.1 wt% of LaB6 to the steel, the bending strength and the fracture toughness were improved from 3290 MPa and 25.6 MPam1/2 to 4018 MPa and 29.4 MPam1/2, respectively. The TEM analysis demonstrated three types of reaction products by the LaB6 addition: the amorphous phase, the core-shell structure and the La2O3 phase. The impurity elements such as the Mg, Al, Si, S, Ca, and O were absorbed following the LaB6 addition. Moreover, the deoxidization effect caused by the LaB6 addition promoted the sintering at a high-temperature period which contributed to the bending strength and fracture toughness improvement.