The electrochemical CO2 reduction reaction (CO2RR) has received widespread attention as a promising method for producing sustainable chemicals and mitigating the global warming. Here, we demonstrate a general and facile synthetic route for the metal-nitrogen-carbon (M-N-C) type catalyst by simply calcinating metal acetate and urea with commercial carbon black, which have potential application in CO2RR. The synthesized Ni-NC-600 catalyst has the structure of single Ni atom coordinated with one N atom and three C atoms (Ni-N1C3), which is suggested by X-ray absorption spectroscopy. The Ni-NC-600 catalyst exhibits high CO2RR catalytic performance and a high CO Faraday efficiency above 98% in a wide potential range from −0.7 to −1.3 V (vs. reversible hydrogen electrode (RHE)), superior to most of the reported Ni-N-C catalysts. This work has developed a facile strategy to synthesize high performance CO2RR catalyst.
Hexagonal and triangular monodisperse Fe3O4 nanosheets have been synthesized via a two-step microemulsion solvothermal approach in which uniform Fe3O4 nanoparticles are first prepared and then these hydrophobic nanocrystals are dispersed in a uniform microemulsion environment as "seeds" for further re-growth through a secondary solvothermal process. The growth of anisotropic morphologies has been explained by the presence and orientation of twin planes in the face-centered cubic Fe3O4 which direct the shape of the growing particles. In particular, reentrant grooves resulting from twin planes are favorable sites for the addition of adatoms, leading to anisotropic growth. Triangular nanosheets are believed to contain one twin face which directs the growth of the primary particles in two dimensions. Hexagonal nanosheets are believed to contain two parallel planes that allow the growth edges to regenerate one another. The growth mechanism is evidenced by the analysis of high-resolution transmission electron microscopy (HRTEM) results and the as-prepared Fe3O4 nanoparticles have been shown to be an effective catalyst in the synthesis of quinoxaline.