Forthrightly monitoring ferroptosis induced by endoplasmic reticulum stresses through fluorescence lifetime imaging of microviscosity increases with a specific rotor

To test the hypothesis that the microviscosity changes of Endoplasmic Reticulum(ER) can be a useful indicator of ferroptosis promoted by ER Stresses(ERS), a new ER targeting viscosity rotor, L-Vis-1 was developed and applied in the quantitation of viscosity by FLIM imaging in live cells. The FLIM imaging exhibited an excellent resolution almost as good as the corresponding confocal imaging, more significantly, during ferroptosis processes promoted by different types of ERS, the viscosity increas...     

Global Regularity of 3D Nonhomogeneous Incompressible Micropolar Fluids

This paper is concerned with the global well-posedness of strong and classical solutions for the 3D nonhomogeneous incompressible micropolar equations with vacuum. We prove that the problem (1.1)–(1.5) has a unique global strong/classical solution \((\rho,u,w)\), provided \(\mu_{1}\) is sufficiently large, or \(\|\rho_{0}\|_{L^{\infty}}\) or \(\|\rho_{0}^{1/2}u_{0}\| ^{2}_{L^{2}}+\|\rho_{0}^{1/2}w_{0}\|^{2}_{L^{2}}\) is small enough.

     

Nonlinear Jordan Higher Derivations of Triangular Algebras

In this paper, we prove that any nonlinear Jordan higher derivation on triangular algebras is an additive higher derivation. As a byproduct, we obtain that any nonlinear Jordan derivation on nest algeb...     

基于B3PyMPM∶Cs高效叠层OLED器件的制备

以B 3 PyMPM∶Cs/Al/HAT-CN作为电荷生成单元制备高效叠层绿色磷光有机电致发光器件,叠层器件的最大电流效率和最大流明效率分别为172.2 cd/A和111.0 lm/W,在5 mA/cm^2电流密度下,叠层器件的电压和亮度分别为传统器件的2.04倍和2.84倍.为了探究叠层器件性能优于传统器件的原因,研究了电荷生成单元内的电荷产生和注入过程,以及薄层铝对电子注入特性和电荷生成单元稳定性的影响.实验结果表明,电荷能够有效地在电荷生成单元内产生并顺利注入电子传输层中,B3PyMPM∶Cs和HAT-CN间Al薄层的插入能够进一步提高电子注入效率及器件结构的稳定性.     

Collective sustained oscillations in excitable small-world networks: the moderate fundamental loop or the minimum Winfree loop?

Nonlinear Dynamics - The problem of self-sustained oscillations in excitable complex networks is the central issue under investigation, among which the exploration of the key factors in determining...     

Tea-derived carbon materials as anode for high-performance sodium ion batteries

Sodium-ion batteries (SIB) have attracted widespread attention in large-scale energy storage fields owing to the abundant reserve in the earth and similar properties of sodium to lithium. Biomass-based carbon materials with low-cost, controllable structure, simple processing technology, and environmental friendliness tick almost all the right boxes as one of the promising anode materials for SIB. Herein, we present a simple novel strategy involving tea tomenta biomass-derived carbon anode with enhanced interlayer carbon distance (0.44 nm) and high performance, which is constructed by N,P co-doped hard carbon (Tea-1100-NP) derived from tea tomenta. The prepared Tea-1100-NP composite could deliver a high reversible capacity (326.1 mAh/g at 28 mA/g), high initial coulombic efficiency (ICE = 90% at 28 mA/g), stable cycle life (262.4 mAh/g at 280 mA/g for 100 cycles), and superior rate performance (224.5 mAh/g at 1400 mA/g). Experimental results show that the excellent electrochemical performance of Tea-1100-NP due to the high number of active N,P-containing groups, and disordered amorphous structures provide ample active sites and increase the conductivity, meanwhile, large amounts of microporous shorten the Na⁺ diffusion distance as well as quicken ion transport. This work provides a new type of N,P co-doped high-performance tomenta-derived carbon, which may also greatly promote the commercial application of SIB.     

绿色双溶剂法制备高效稳定钙钛矿太阳能电池

采用毒性小、环境友好的乙二醇甲醚(ethylene glycol monomethyl ether,EGME)与水混合的双溶剂(体积比为1∶1)溶解CsBr,通过提高CsBr的溶解度,减少了后续CsBr的甲醇溶液的旋涂遍数,简化了电池制备流程。通过优化CsBr的甲醇溶液的旋涂遍数发现,在旋涂1遍200 mg·mL^-1 CsBr的水/EGME溶液的基础上旋涂2遍15 mg·mL^-1 CsBr的甲醇溶液,所制备的CsPb-Br₃钙钛矿太阳能电池(perovskite solar cells,PSCs)拥有最佳的性能,实现了1.44 V的开路电压(open-circuit voltage,V_OC),6.26mA·cm^-2的短路电流密度(short circuit current density,J_SC),74.57%的填充因子(fill factor,FF)及最高6.72%的光电转换效率(pho-toelectric conversion efficiency,PCE)。     

Breaking Surface Atomic Monogeneity of Rh2P Nanocatalysts by Defect-Derived Phosphorus Vacancies for Efficient Alkaline Hydrogen Oxidation

Breaking atomic monogeneity of catalyst surfaces is promising for constructing synergistic active centers to cope with complex multi-step catalytic reactions. Here, we report a defect-derived strategy for creating surface phosphorous vacancies (P-vacancies) on nanometric Rh₂P electrocatalysts toward drastically boosted electrocatalysis for alkaline hydrogen oxidation reaction (HOR). This strategy disrupts the monogeneity and atomic regularity of the thermodynamically stable P-terminated surfaces. Density functional theory calculations initially verify that the competitive adsorption behavior of H_ad and OH_ad on perfect P-terminated Rh₂P{200} facets (p-Rh₂P) can be bypassed on defective Rh₂P{200} surfaces (d-Rh₂P). The P-vacancies enable the exposure of sub-surface Rh atoms to act as exclusive H adsorption sites. Therein, the H_ad cooperates with the OH_ad on the peripheral P-sites to effectively accelerate the alkaline HOR. Defective Rh₂P nanowires (d-Rh₂P NWs) and perfect Rh₂P nanocubes (p-Rh₂P NCs) are then elaborately synthesized to experimentally represent the d-Rh₂P and p-Rh₂P catalytic surfaces. As expected, the P-vacancy-enriched d-Rh₂P NWs catalyst exhibits extremely high catalytic activity and outstanding CO tolerance for alkaline HOR electrocatalysis, attaining 5.7 and 14.3 times mass activity that of p-Rh₂P NCs and commercial Pt/C, respectively. This work sheds light on breaking the surface atomic monogeneity for the development of efficient heterogeneous catalysts.     

Experimental and theoretical studies of carbon monoxide oxidation over W/Cu/Ce trimetallic oxides: the effect of W addition

It is a significant method to prepare highly dispersed polymetallic oxides using in-situ doping metal organic frameworks as precursors. Herein, a series of straw-like W/Cu/Ce trimetallic oxides were prepared by using phosphotungstic ionic liquid@Ce-based metal organic framework adsorbing with copper acetylacetonate as precursors. The effect of W content on catalytic activity of W/Cu/Ce trimetallic oxides for carbon monoxide (CO) oxidation was well-investigated. Comprehensive characterization methods and density functional theory calculations were adopted to reveal the property changes of Cu/CeO₂ catalyst by the addition of W. The results demonstrated that W, Cu, and Ce are highly dispersed in the prepared W/Cu/Ce trimetallic oxides, and adding proper amount of W can improve the activity of the catalyst. H₂ temperature-program reduction profiles, X-ray photoelectron spectroscopy, in-situ diffuse reflectance infrared Fourier transform spectroscopy, and density functional theory calculations clearly revealed that after the addition of W, the strength of Ce-O bond is weakened, the oxygen vacancy is increased, and the adsorption of CO is enhanced, respectively, which are vital reasons for its high catalytic activity. In addition, the CO oxidation reaction pathway over prepared W/Cu/Ce trimetallic oxides based on the Mars-van Krevelen mechanism was studied, and the results exhibited that CO can wrest the lattice oxygen of W/Cu/Ce trimetallic oxides to form CO₂, which is also proved to be the rate-determining step in reaction process.