High‐Efficiency Perovskite Solar Cells Enabled by Anatase TiO2 Nanopyramid Arrays with an Oriented Electric Field

One‐dimensional (1D) nanostructured oxides are proposed as excellent electron transport materials (ETMs) for perovskite solar cells (PSCs); however, experimental evidence is lacking. A facile hydrothermal approach was employed to grow highly oriented anatase TiO₂ nanopyramid arrays and demonstrate their application in PSCs. The oriented TiO₂ nanopyramid arrays afford sufficient contact area for electron extraction and increase light transmission. Moreover, the nanopyramid array/perovskite system exhibits an oriented electric field that can increase charge separation and accelerate charge transport, thereby suppressing charge recombination. The anatase TiO₂ nanopyramid array‐based PSCs deliver a champion power conversion efficiency of approximately 22.5 %, which is the highest power conversion efficiency reported to date for PSCs consisting of 1D ETMs. This work demonstrates that the rational design of 1D ETMs can achieve PSCs that perform as well as typical mesoscopic and planar PSCs.     

An ultra compact photonic crystal wavelength division demultiplexer using resonance cavities in a modified Y-branch structure

An ultra small size 4-channel wavelength division demultiplexer based on 2D photonic crystal modified Y-Branch, suitable for integration, is proposed in this paper. The output wavelengths of designed structure can be tuned for communication applications (around 1550 nm) by choosing suitable defect parameters in the corner of each resonance cavity and output waveguides. The cross section of the structure is 313.28 μm² (17.8 μm × 17.6 μm) and desirable for integration based on popular planar technology. The bandwidth of each channel is near to 1 nm and the channel spacing is approximately 3.5 nm and wavelengths of demultiplexer channels are 1548.8 nm, 1551.9 nm, 1555.4 nm and 1559.3 nm respectively. Also, the crosstalk is between −33.1855 dB and −10.4947 dB. Furthermore, the mean values of the crosstalk and quality factor are −22.54 dB and 1496.7 respectively.     

Existence of an extremal ground state energy of a nanostructured quantum dot

This paper is concerned with two rearrangement optimization problems. These problems are motivated by two eigenvalue problems which depend nonlinearly on the eigenvalues. We consider a rational and a quadratic eigenvalue problem with Dirichlet’s boundary condition and investigate two related optimization problems where the goal function is the corresponding first eigenvalue. The first eigenvalue in the rational eigenvalue problem represents the ground state energy of a nanostructured quantum dot. In both the problems, the admissible set is a rearrangement class of a given function.     

Rapid and Convenient Method for the Synthesis of Symmetrical Disulfides

Abstract

We present here the results on the use of 1,3,5-triazo-2,4,6-triphosphorine-2,2,4,4,6,6-hexachloride as an efficient promoter in the conversion of thiols to the corresponding symmetrical disulfides under solvent-free conditions. Aromatic thiols bearing electron donating and electron withdrawing groups, heteroaromatic, and alkyl thiols reacted efficiently to afford excellent yields of disulfides in short reaction times after easy work-up. Different functional groups including carboxyl, methoxy, methylthio, and halogen are tolerated.

Supplementary materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfer, and Silicon and the Related Elements for the following free supplemental files: Additional figures and tables.     

Three-Component Synthesis and 1,3-Dipolar Cycloaddition of Highly Functionalized Pyrans with Nitrile Oxides: Easy Access to 1,2,4-Oxadiazoles

Three-component reaction of 1-[(4-chlorophenyl)sulfanyl]acetone, malononitrile, and substituted aromatic aldehydes in the presence of sodium ethoxide under simple mixing at ambient temperature for 5–8 min afforded highly functionalized 4H-pyrans in good to excellent yields. 1,3-Dipolar cycloaddition of nitrile oxides over the nitrile functionality of the 4H-pyrans furnished 1,2,4-oxadiazoles in moderate yields.

Supplementary materials are available for this article. Go to the publisher's online edition of Synthetic Communications® for full experimental and spectral details.     

Impact of Surface Roughness on Flow Physics and Entropy Generation in Jet Impingement Applications

In this paper, a numerical investigation was performed of an air jet incident that normally occurs on a horizontal heated plane. Analysis of flow physics and entropy generation due to heat and friction is included using a simple easy-to-manufacture, surface roughening element: a circular rib concentric with the air jet. This study shows how varying the locations and dimensions of the rib can deliver a favorable trade-off between entropy generation and flow parameters, such as vortex generation and heat transfer. The performance of the roughness element was tested at three different radii; R/D = 1, 1.5 and 2, where D was the jet hydraulic diameter and R was the radial distance from the geometric center. At each location, the normalized rib height (e/D) was increased from 0.019 to 0.074 based on an increment of (e/D) = 0.019. The jet-to-target distance was H/D = 6 and the jet Reynolds number (Re) ranged from 10,000 to 50,000 Re, which was obtained from the jet hydraulic diameter (D), and the jet exit velocity (U). All results are presented in the form of entropy generation due to friction and heat exchange, as well as the total entropy generated. A detailed comparison of flow physics is presented for all ribs and compared with the baseline case of a smooth surface. The results show that at higher Reynolds numbers, adding a rib of a suitable height reduced the total entropy (St) by 31% compared to the no rib case. In addition, with ribs of heights 0.019, 0.037 and 0.054, respectively, the entropy generated by friction (Sf) was greater than that due to heat exchange (Sh) by about 42%, 26% and 4%, respectively. The rib of height e/D = 0.074 produced the minimum S_t at R/D = 1. As for varying R/D, varying rib location and Re values had a noticeable impact on Sh, Sf and (St). Placing the rib at R/D = 1 gave the highest total entropy generation (St) followed by R/D = 1.5 for all Re. Finally, the Bejan number increased as both rib height and rib location increased.     

nor 3′-Demethoxyisoguaiacin from Larrea tridentata Is a Potential Alternative against Multidrug-Resistant Bacteria Associated with Bovine Mastitis

Bovine mastitis is one of the most common diseases in dairy cows, and it causes significant economic losses in dairy industries worldwide. Gram-positive and Gram-negative bacteria can cause bovine mastitis, and many of them have developed antimicrobial resistance. There is an urgent need for novel therapeutic options to treat the disease. Larrea tridentata-derived compounds represent an important potential alternative treatment. The aim of the present study was to isolate and characterize antibacterial compounds from Larrea tridentata against multidrug-resistant bacteria associated with bovine mastitis. The L. tridentata hydroalcoholic extract (LTHE) exhibited antibacterial activity. The extract was subjected to a bipartition, giving an aqueous fraction (moderate antibacterial activity) and an organic fraction (higher antibacterial activity). Chromatographic separation of the organic fraction enabled us to obtain four active sub-fractions. Chemical analyses through HPLC techniques were conducted for the LTHE, fractions, and sub-fraction Ltc1-F3, from which we isolated two compounds, characterized by ¹H and ¹³C NMR analyses. Compound nor-3 demethoxyisoguaiacin exhibited the best antibacterial activity against the evaluated bacteria (MIC: 0.01–3.12 mg/mL; MBC: 0.02–3.12 mg/mL). The results indicated that nor-3 demethoxyisoguaiacin can be used as an alternative treatment for multidrug-resistant bacteria associated with mastitis.     

1-(对甲苯基)-2-(三对甲苯基-5-亚磷酰基)乙醛的汞(Ⅱ)配合物的X射线晶体学、光谱表征和理论计算研究（英文）

通过2-溴-1-(对甲苯基)乙醛与三(对甲苯基)膦的反应制备α-磷配体:1-(对甲苯基)-2-(三对甲苯基-5-亚磷酰基)乙醛(L)。氯化镉和溴化汞与L分别反应,生成配合物[Cd(L)Cl_2]_2(C1)和[Hg(L)(μ_2-Br)Br]_2(C2)。用IR和NMR(~1H,~(13)C,~(31)P)对配合物进行了表征。通过单晶X射线衍射测定了C2的结构,并在B3LYP/6-31G~*水平对C2的结构进行了DFT计算研究,以揭示C2的复合反应位点与Schiff碱等亲核基团的相互作用。