Constructing Metal(II)-Sulfate Site Catalysts toward Low Overpotential Carbon Dioxide Electroreduction to Fuel Chemicals.

Precise regulation of the active site structure is an important means to enhance the activity and selectivity of catalysts in CO2 electroreduction. Here, we creatively introduce anionic groups, which can not only stabilize metal sites with strong coordination ability but also have rich interactions with protons at active sites to modify the electronic structure and proton transfer process of catalysts. This strategy helps to convert CO2 into fuel chemicals at low overpotentials. As a typical example, a composite catalyst, CuO/Cu-NSO4/CN, with highly dispersed Cu(II)-SO4 sites has been reported, in which CO2 electroreduction to formate occurs at a low overpotential with a high Faradaic efficiency (-0.5 V vs. RHE, FEHCOO-=87.4%). Pure HCOOH is produced with an energy conversion efficiency of 44.3% at a cell voltage of 2.8 V. Theoretical modeling demonstrates that sulfate promotes CO2 transformation into a carboxyl intermediate followed by HCOOH generation, whose mechanism is significantly different from that of the traditional process via a formate intermediate for HCOOH production.

The site pair matching of a tandem Au/CuO-CuO nanocatalyst for promoting the selective electrolysis of CO2 to C2 products.

Tandem catalysis, in which a CO2-to-C2 process is divided into a CO2-to-CO/*CO step and a CO/*CO-to-C2 step, is promising for enhancing the C2 product selectivity when using Cu-based electrochemical CO2 reduction catalysts. In this work, a nanoporous hollow Au/CuO-CuO tandem catalyst was used for catalyzing the eCO2RR, which exhibited a C2 product FE of 52.8% at -1.0 V vs. RHE and a C2 product partial current density of 78.77 mA cm-2 at -1.5 V vs. RHE. In addition, the C2 product FE stably remained at over 40% over a wide potential range, from -1.0 V to -1.5 V. This superior performance was attributed to good matching in terms of the optimal working potential and charge-transfer resistance between CO/*CO-production sites (Au/CuO) and CO/*CO-reduction sites (CuO). This site pair matching effect ensured sufficient supplies of CO/*CO and electrons at CuO sites at the working potentials, thus dramatically enhancing the formation rate of C2 products.

Synthesis of ultrathin Ni nanosheets for semihydrogenation of phenylacetylene to styrene under mild conditions.

The synthesis of ultrathin metal nanosheets (NSs) attracts broad scientific and technological interest, and it still remains a challenge for non-noble metals like nickel due to their intrinsic cubic symmetry and high surface energy. Herein, we report a NiO intermediated solvothermal method towards the synthesis of ultrathin Ni NSs (thickness < 3 nm) using N,N-dimethylformamide as the solvent and n-butylamine as the shape controlling reagent. The growth of the ultrathin Ni NSs follows an intermediate mechanism which was proved by the results obtained by means of transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray absorption spectra (XAS) and X-ray photoelectron spectroscopy (XPS). Under solvothermal conditions, the nickel acetylacetonate precursor was first reduced to a NiO NS intermediate, then reduction occurred and NiO NSs were reduced to Ni NSs. The synthesized ultrathin Ni NSs predominately in a metallic state showed high selectivity (88.0-92.0%) towards styrene (ST) in the phenylacetylene (PA) semihydrogenation reaction under mild conditions (323 K, 1 atm of hydrogen) in a broad PA conversion range (2.0-98.0%). The low coverage of oxygen atoms on the Ni NS surface is proposed to account for the high ST selectivity, as indicated by density functional theory (DFT) calculations.