Structure-guided design of potent JAK1-selective inhibitors based on 4-amino-7H-pyrrolo[2,3-d]pyrimidine with anti-inflammatory efficacy.

In a continuous effort to develop Janus kinase 1 (JAK1)-selective inhibitors, a novel series of 4-amino-7H-pyrrolo[2,3-d]pyrimidine derivatives bearing the piperidinyl fragment were designed and synthesized according to a combination strategy. Through enzymatic assessments, the superior compound 12a with an IC50 value of 12.6 nM against JAK1 was identified and a 10.7-fold selectivity index over JAK2 was achieved. It was indicated that 12a displayed considerable effect in inhibiting the pro-inflammatory NO generated from lipopolysaccharide (LPS)-induced RAW264.7 macrophages, while on normal RAW264.7 cells, 12a exerted a weak cytotoxicity effect (IC50 = 143.3 µM). Furthermore, H&E stain assay demonstrated the conspicuous capacity of 12a to suppress CCl4-induced hepatic fibrosis levels in a dose-dependent manner in vivo. The binding model of 12a ideally reflects the excellent activity of JAK1 over the homologous kinase JAK2. Overall, 12a, a JAK1-selective inhibitor, exhibited potential for liver fibrosis and inflammatory diseases.

Electrolyte effect for carbon dioxide reduction reaction on copper electrode interface: A DFT prediction.

An insightful understanding of the interaction between the electrolyte and reaction intermediate and how promotion reaction occurs of electrolyte is challenging in the electrocatalysis reaction. Herein, theoretical calculations are used to investigate the reaction mechanism of CO2 reduction reaction to CO with different electrolytes at the Cu(111) surface. By analyzing the charge distribution of the chemisorbed CO2 (CO2 δ-) formation process, we find that the charge transfer is from metal electrode transfer to CO2 and the hydrogen bond interaction between electrolytes and CO2 δ- not only plays a key role in the stabilization of CO2 δ- structure but also reduces the formation energy of *COOH. In addition, the characteristic vibration frequency of intermediates in different electrolyte solutions shows that H2O is a component of HCO3 -, promoting CO2 adsorption and reduction. Our results provide essential insights into the role of electrolyte solutions in interface electrochemistry reactions and help understand the catalysis process at the molecular level.

Enhancement of Impact Abrasion Resistance Performances of White Cast Iron Utilizing Ti3AlC2.

Al-Ti-C master alloy agent is currently the most promising grain refiner. This work investigates the influence of Ti3AlC2 addition (1.0-3.0 wt.%) on the microstructure of a hypoeutectic cast iron (4.7 wt.% Cr, 2.3 wt.% C). Microstructures of the samples were examined by SEM (scanning electron microscope). It was demonstrated that the added Ti3AlC2 did reduce the size of coarse primary carbides. The XRD (X-ray diffraction) pattern shows that Ti3AlC2 is decomposed into TiC in the alloy substrate. The EDS (energy dispersive spectrometer) interfacial element analysis shows that TiC combines well with the matrix interface. As the Ti3AlC2 amount was increased, the finest microstructure was achieved. When 2 wt.% Ti3AlC2 was added, the wear-resistance property of the material improved and became two times harder than the former. However, when 3% Ti3AlC2 was added, TiC gathered at the crystal boundary, which caused a decrease in the wear resistance of the material.

Ultrathin Ce-doped La2O3nanofilm electrocatalysts for efficient oxygen evolution reactions.

It is still highly desired to develop efficient, resource-abundant and inexpensive electrocatalysts to improve the sluggish kinetics of oxygen evolution reaction (OER) in electrochemical water splitting systems. In this work, the large-area ultrathin (2.52 nm thick) Ce-doped La2O3nanofilms were developed via a facile and reliable ionic layer epitaxy method with different Ce content. The ultrathin Ce-doped La2O3nanofilm with optimum composition of La1.22Ce0.78O3exhibited an excellent OER performance with a very low overpotential of 221 mV at 10 mA cm-2and a small Tafel slope of 33.7 mV dec-1. A remarkable high mass activity of 6263.2 A g-1was also obtained from ultrathin La1.22Ce0.78O3nanofilm at the overpotential of 221 mV. Such a high mass activity was three orders of magnitude higher than state-of-the-art commercial IrO2powders (3.8 A g-1) and more than 30 times higher than La2O3nanofilm (196.7 A g-1) without Ce doping at the same overpotential. This high mass activity was even significantly higher than other recently reported typical OER catalysts. The substantial OER performance gain by the Ce doping was attributed to the improved conductivity and electrochemical active surface areas of nanofilms as a result of favorable tuning on the charge transfer and electronic structures. This work provides a promising approach to develop high-performance two-dimensional (2D) electrocatalysts by effective heteroatom doping strategy.

Creating Fluorine-Doped MoS2 Edge Electrodes with Enhanced Hydrogen Evolution Activity.

The edge sites of MoS2 are catalytically active for hydrogen evolution reactions (HER). However, pristine edge sites usually contain only intrinsic atoms or defects, limiting the tuning of on-site hydrogen species adsorption and desorption, the critical steps for HER. In addition, the number of atoms on pristine edges is small compared to that of electrochemically inert atoms in bulk. Thus, it is desirable to develop a scalable technique of creating a large number of highly HER-active edge sites. Here, a plasma etching strategy is developed for creating MoS2 edge electrodes with a controllable number of active sites that enable the quantitative characterization of their HER activity using a local probe method. Fluorine atoms with large electronegativity are doped on the MoS2 edge sites that lead to a fivefold activity enhancement compared to that from pristine edges and is attributed to the more moderate binding energy for hydrogen species. The scalability of such a method is further demonstrated by activating MoS2 catalyst in macroscopic quantities with enhanced HER performance and stability. The work provides two-dimensional materials as a platform for understanding the doping effect on the edge sites at atomic-level, and offers a novel route for the design of efficient catalysts.

Mesoporous Ultrathin In2O3 Nanosheet Cocatalysts on a Silicon Nanowire Photoanode for Efficient Photoelectrochemical Water Splitting.

Vertical Si nanowire (NW) arrays are a promising photoanode material in the photoelectrochemical (PEC) water splitting field because of their highly efficient light absorption capability and large surface areas for PEC reactions. However, Si NW arrays always suffer from high overpotential, low photocurrent density, and low applied bias photon-to-current efficiency (ABPE) due to their low surface catalytic activity and intense charge recombination. Here, we report an efficient oxygen evolution cocatalyst of optically transparent, mesoporous ultrathin (2.47 nm thick) In2O3 nanosheets, which are coupled on the top of Si NW arrays. Combined with a conformal TiO2 thin film as an intermediate protective layer, this Si NW/TiO2/In2O3 (2.47 nm) heterostructured photoanode exhibited an extremely low onset potential of 0.6 V vs reversible hydrogen electrode (RHE). The Si NW/TiO2/In2O3 (2.47 nm) photoanode also showed a high photocurrent density of 27 mA cm-2 at 1.23 V vs RHE, more than 1 order of magnitude higher than that of the Si NW/TiO2 photoanodes. This improvement in solar water splitting performance was attributed to the significantly promoted charge injection efficiency as a result of the In2O3 nanosheet coupling. This work presents a promising pathway for developing efficient Si-based photoanodes by coupling ultrathin 2D cocatalysts.