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We reported a scalable sol–gel method for the preparation of Sr<sub>0.3</sub>Pb<sub>0.7</sub>TiO<sub>3</sub>/CoFe<sub>2</sub>O<sub>4</sub> core–shell magnetic nanocomposite with a finely controlled shell and evaluated its efficiency as an electrochemical sensor for the selective detection of 3,4-diaminotoluene.
The use of electrocatalysts with low metal content (metal-deficient) or metal free for the hydrogen evolution reaction (HER) can prevent or decrease metal ion release, which reduces environmental impact; development of such catalysts with high activity and durability over the whole pH range is thus highly desired but still remains a huge challenge. Herein, we describe the direct growth of a film consisting of interconnected Co-entrapped, N-doped carbon nanotubes on carbon cloth using chemical vapor deposition from dicyanodiamine using a Co3 O4 nanowire array as catalyst. This integrated architecture is used as a flexible 3D electrode for the electrolytic hydrogen evolution with outstanding catalytic activity and durability in acidic media. Moreover, this electrode is also highly efficient under neutral and basic conditions. It offers us an attractive carbon-based metal-deficient HER catalyst outperforming most transition-metal and all metal-free/deficient catalysts.
Microporous graphitic carbon (mp-C) derived from the pyrolysis of α-, β-, and γ-cyclodextrins exhibited photocatalytic activity in CO<sub>2</sub>-saturated acetonitrile-water upon irradiation with UV-Vis light and in the presence of triethanolamine, forming H<sub>2</sub> (19 μmol h<sup>-1</sup>) and CO (23 μmol h<sup>-1</sup>) accompanied by a lesser proportion of CH<sub>4</sub> (4 μmol h<sup>-1</sup>). The most efficient was the mp-C material derived from α-cyclodextrin (mp-C<sub>α</sub>) and having a pore dimension of 0.68 nm. The process also occured, although to a much lesser extent, under simulated sunlight or with UV-Vis irradiation in the absence of a sacrificial agent, with H<sub>2</sub>O being the electron donor. The origin of the CO was proved by isotopic <sup>13</sup>C labelling experiments. Photocurrent measurements proved the occurrence of charge separation and the increase in photocurrent intensity in the presence of CO<sub>2</sub>. Transient absorption spectroscopy was used to detect the charge separate state decay in the microsecond time scale and proved that a fraction of the photogenerated electrons were able to react with CO<sub>2</sub>.
The complete mol-ecule of the title compound, C(14)H(16)N(2)S(2), is generated by a crystallographic inversion centre. The thio-phene residue is close to being coplanar with the imine group [C-C-C-N torsion angle = 6.5 (2)°], and the conformation about the imine C=N bond [1.281 (2) Å] is E. In the crystal, the three-dimensional architecture is consolidated by C-H⋯N, C-H⋯π and S⋯S [3.3932 (7) Å] inter-actions.
The mol-ecule of the title compound, C(8)H(6)N(2)OS(2), has a V shape with two five-membered rings attached to a methyl-ene C atom. All non-H atoms are approximately coplanar (r.m.s. deviation = 0.096 Å). In the crystal, mol-ecules are linked by N-H⋯O hydrogen bonds into layers. The thio-phene ring is disordered over two positions; the major orientation has an occupancy of 0.683 (3). is there an intramolecular N---H...S bond?
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.