2,859 publications from this institution
Developing nanoporous nanoarray electrocatalysts for efficient water oxidation in environmentally benign media is highly desired but still remains a key challenge. In this communication, we report the fabrication of a nanoporous crystalline CoB<sub>2</sub>O<sub>4</sub> nanowire array on Ti mesh (CoB<sub>2</sub>O<sub>4</sub>/TM) from a Co(OH)F nanowire array on Ti mesh (Co(OH)F/TM) via an anion-exchange reaction. As a three dimensional (3D) catalyst electrode for water oxidation, CoB<sub>2</sub>O<sub>4</sub>/TM exhibits superior catalytic activity and needs an overpotential of only 446 mV to drive a geometrical catalytic current density of 10 mA cm<sup>-2</sup> in 0.1 M potassium borate (pH = 9.2). Notably, this catalyst also shows strong long-term electrochemical durability with high turnover frequency values of 0.19 and 0.81 mol O<sub>2</sub> per s at overpotentials of 400 and 500 mV, respectively.
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.
Abstract Mixed micellization behavior of an amphiphilic phenothiazine drug promazine hydrochloride (PMZ) in the presence of conventional dodecyltrimethylammonium bromide (DTAB) as well as gemini 1,4-bis( N -dodecyl- N , N -dimethylammonium)butane bromide (12-4-12) cationic surfactants has been studied at four different fixed temperatures and compositions by conductometric technique. The experimental data have been analysed by considering different theoretical models of Clint, Rubingh, Motomura and Rodenas. The cmc and cmc id values indicate mixed micelle formation between the components and strong synergism is observed in the mixed systems. The micellar (actual) mole fractions of surfactants ( χ 1 Rub , χ 1 M , χ 1 Rod and χ 1 id ), calculated on the basis of different theoretical proposed models used in the present study, show greater contribution of surfactants in mixed micelles. Activity coefficients ( f 1 and f 2 ) are always less than unity indicating nonideality in the systems. Thermodynamic parameters are also evaluated and discussed which suggest that at higher temperatures dehydration of hydrophobic part of the drug takes place.
Significant twists between the aromatic rings are evident in the structure of the title compound, C(16)H(12)F(3)N(3)O(2)S. With reference to the pyrazole plane, the N- and C-bound benzene rings form dihedral angles of 57.12 (11) and 29.75 (11)°, respectively. The dihedral angle between the benzene rings is 52.82 (11)°. The presence of N-H⋯O(sulfonamide) and N-H⋯N(pyrazole) hydrogen bonds lead to supra-molecular tubes along the b-axis direction. These are connected into layers via C-H⋯O inter-actions involving a bifurcated O atom (not involved in the N-H⋯O hydrogen bonding). Layers stack along the a-axis direction.
Copper nanoparticles (NPs) supported on a series of undoped and doped graphene materials (Gs) have been obtained by pyrolysis of alginate or chitosan biopolymers, modified or not with boric acid, containing Cu(2+) ions at 900 °C under inert atmosphere. The resulting Cu-G materials containing about 17 wt % Cu NPs (from 10 to 200 nm) exhibit high catalytic activity for the dehydrogenative coupling of silanes with alcohols. The optimal material consisting on Cu-(B)G is more efficient than Cu NPs on other carbon supports.