2,859 publications from this institution
A Fe-doped Ni<sub>3</sub>S<sub>2</sub>particle film grown on nickel foam (Fe<sub>11.8%</sub>-Ni<sub>3</sub>S<sub>2</sub>/NF) behaves as a high-efficiency and robust oxygen evolution electrode in strongly alkaline solution.
The photocatalytic activity of protonated ordered mesoporous carbon nitride (pom-CN) was significantly improved by assembling anionic [Mo<sub>3</sub>S<sub>13</sub>]<sup>2-</sup> clusters as cocatalysts onto the surface and channel of pom-CN via electrostatic interactions. This work demonstrates the feasibility of employing solution chemistry to assemble co-catalysts in the form of ionic clusters as building blocks into a photosynthetic architecture.
Electrochemical reduction has been regarded as a sustainable strategy to tackle energy-intensive operations by the Haber-Bosch process achieving catalytic conversion of N<sub>2</sub> to NH<sub>3</sub> under mild conditions. However, the challenge of N<sub>2</sub> electroconversion emphasizes the requirement of efficient electrocatalysts. In this paper, we report the development of porous bromide-derived Ag film (BD-Ag/AF) as an efficient electrocatalyst for N<sub>2</sub> reduction reaction. During electrochemical test, Br<sup>-</sup> anions are released and adsorbed onto the surfaces of the electrode, suppressing hydrogen evolution reaction. Such BD-Ag/AF shows a high Faradaic efficiency of 7.36% at -0.6 V vs reversible hydrogen electrode in 0.1 M Na<sub>2</sub>SO<sub>4</sub>, which is higher than that (0.38%) of porous Ag film without Br<sup>-</sup> anions. Moreover, it exhibits excellent long-term electrochemical durability.
In the title compound, C(26)H(21)N(3)O, the phenyl ring of the 4-amino-anti-pyrine group and the heterocyclic five-membered ring along with its substituents, except for the N-bound methyl group (r.m.s. deviation = 0.0027 Å), form a dihedral angle of 54.20 (5)°. Two S(6) ring motifs are formed due to intra-molecular C-H⋯N and C-H⋯O hydrogen bonds. In the crystal, mol-ecules are linked into supra-molecular chains along the a-axis direction via C-H⋯O contacts.