2,859 publications from this institution
Abstract It is highly needed but still a difficult challenge to achieve energy‐saving electrolytic hydrogen generation. In this communication, we describe the first use of iron phosphide nanosheets array on Ni foam as a high‐active and durable catalyst for electrochemical hydrazine oxidation reaction (HzOR) in alkaline media. The high hydrogen‐evolving activity of this catalyst electrode and the substitution of sluggish oxygen evolution with thermodynamically more favorable HzOR enables the construction of a stable two‐electrode energy‐efficient electrolytic hydrogen generation system capable of driving 125 mA cm −2 at a cell voltage of 0.5 V to in 1.0 M KOH with 0.5 M hydrazine.
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.
In this approach, binary tin oxide doped ytterbium oxide nanosheets (SnO2.YbO NSs) were synthesized in an alkaline phase using under low-temperature facile hydrothermal technique. Traditional methods such as UV–Visible spectroscopy, Fourier Transform Infra-Red Spectroscopy (FTIR), Powder X-ray diffraction (XRD), Field Emission Scanning Microscopy (FESEM) equipped with X-ray electron dispersive spectroscopy (XEDS), and X-ray photoelectron spectroscopy (XPS) were used to fully characterize the prepared SnO2.YbO NSs. Fabrication of a thin-coating with doped NSs onto GCE by using 5% nafion conducting binder resulted in development of a selective and enzyme-free penicillin-G sensor probe. A reliable I-V technique was used to perform electrochemical performances of good sensitivity, large LDR, and long-term stability of the desired Penicillin-G sensor (SnO2.YbO NSs/GCE/Nf). With a wide range of Penicillin-G concentration, the proposed calibration plot is noticed good linearity (R2 = 0.9830). Sensitivity and LOD of the sensor were calculated as 24.75 μAμM-1cm−2 and 30.0 pM, respectively based on S/N = 3 formula. Real samples (Human and rabbit serum, milk, and red-sea water) were analyzed with the fabricated SnO2.YbO NSs/GCE/Nf sensor probe and the findings results were acceptable and satisfactory. This approach could be a noble development of in-situ Penicillin-G sensor based on binary SnO2.YbO NSs/GCE/Nf by reliable I-V technique for important sensing applications including beneficial doped nanomaterials and nano-technological system.
Long-range corrected hybrid density functionals (LC-DFT), with range separation parameters optimally tuned to obey Koopmans' theorem, are used to calculate the first-order hyperpolarizabilities of prototypical charge-transfer compounds p-nitroaniline (PNA) and dimethylamino nitrostilbene (DANS) in the gas phase and various solvents. It is shown that LC-DFT methods with default range separation parameters tend to underestimate hyperpolarizabilities (most notably in solution) and that the tuning scheme can sharply improve results, especially in the cases when the standard LC-DFT errors are largest. Nonetheless, we also identify pathological cases (two pyrrole derivatives) for which LC-DFT underestimates the hyperpolarizabilities, regardless of tuning. It is noted that such pathological cases do not follow the usual inverse relation between the hyperpolarizability and amount of exact exchange, and thus this behavior may serve as a diagnostic tool for the adequacy of LC-DFT.
In the title compound, C(24)H(19)N(3)O(2), the partially saturated ring adopts a distorted half-chair conformation with the methyl-ene-C atom closest to the amino-benzene ring lying 0.664 (3) Å out of the plane defined by the five remaining atoms (r.m.s. deviation = 0.1429 Å. The dihedral angle [32.01 (10)°] between the benzene rings on either side of this ring indicates a significant fold in this part of the mol-ecule. The dimeth-oxy-substituted benzene ring is almost orthogonal to the benzene ring to which it is attached [dihedral angle = 72.03 (9)°]. The mol-ecule has been observed previously as the major component of a 1:19 co-crystal with 2-amino-4-(3,4-dimeth-oxy-phen-yl)-5,6-dihydro-benzo[ha]quinoline-3-carbonitrile [Asiri et al. (2011). Acta Cryst. E67, o2873-o2873]. Supra-molecular chains with base vector [201] are formed in the crystal structure via N-H⋯O hydrogen bonds between the amino H atoms of one mol-ecule inter-acting with the meth-oxy O atoms of a neighbouring mol-ecule. The chains are linked into a three-dimensional architecture by C-H⋯π inter-actions.