Visible-light-induced,autopromoted nickel-catalyzed three-component arylsulfonation of 1,3-enynes and mechanistic insights

Science China Chemistry - A light-induced, nickel-catalyzed three-component arylsulfonation of 1,3-enynes in the absence of photocatalyst is reported. This methodology exhibited mild conditions,...     

Optimum design of hierarchical stiffened shells for low imperfection sensitivity

A concept of hierarchical stiffened shell is proposed in this study, aiming at reducing the imperfection sen- sitivity without adding additional weight. Hierarchical stiffened shell is composed of major stiffeners and minor stiff- eners, and the minor stiffeners are generally distributed between adjacent major stiffeners. For various types of geo- metric imperfections, e.g., eigenmode-shape imperfections, hierarchical stiffened shell shows significantly low imper- fection sensitivity compared to traditional stiffened shell. Furthermore, a surrogate-based optimization framework is proposed to search for the hierarchical optimum design. Then, two optimum designs based on two different opti- mization objectives （including the critical buckling load and the weighted sum of collapse loads of geometrically imperfect shells with small- and large-amplitude imperfections） are compared and discussed in detail. The illustrative example demonstrates the inherent superiority of hierarchical stiffened shells in resisting imperfections and the effectiveness of the proposed framework. Moreover, the decrease of imperfection sensitivity can finally be converted into a decrease of structural weight, which is particularly important in the development of large-diameter launch vehicles.     

一类新的Stückelberg全息超导模型

本文研究了含Stückelberg机理的黑洞全息超导模型. 通过选取标量场新的高阶修正形式, 建立了新的Stückelberg黑洞全息超导模型. 通过研究模型参数对标量场凝聚的影响, 发现了当模型参数大于临界值时, 高阶修正可以引起一阶相变. 同时本文还考查了反作用对临界值的影响.     

一类算子方程的正算子解的研究

对算子方程X+A~*X~(-2)A=Q有正算子解的条件做了进一步的研究,得到了方程有正算子解时A,Q,X的范数、谱半径之间新的关系.并给出了算子方程X+A~*X~(-t)A=Q有正算子解的一些条件.     

Effect of pretreatments on the anode structure of solid oxide fuel cells

An important objective in the development of solid oxide fuel cell (SOFC) is to produce thin stabilized zirconia electrolytes that are supported upon the nickel–zirconia composite anode. Although this will reduce some of the problems associated with SOFCs by permitting lower temperature operation, this design may encounter problems during start- up. The first step in a start-up involves the reduction of nickel oxide in the anode to metallic nickel and increase of three-phase boundary will be beneficial for further reaction. In this study, two pretreatment methods are investigated for their effects on the performances of SOFC. Performances of the SOFCs are influenced by the pretreatment conditions, which included exposure of the cells to dilute H₂/O₂ either under open-circuit or closed-circuit conditions before their performance studies. By carrying out the methods, the pretreatment using the closed circuit is found to attain much higher performances effectively and efficiently. Accompanying with SEM and element analysis, increase of three-phase boundary is considered to give rise to changes in the anode microstructure, leading to activation of the anode. Mechanisms of NiO in anode reducing to Ni and porous structure via different pretreatments and their effects on the anode microstructure are proposed.     

Iron-catalyzed remote functionalization of inert C(sp3)–H bonds of alkenes via 1,n-hydrogen-atom-transfer by C-centered radical relay

As an alternative approach to traditional C–H activation that often involved harsh conditions, and vicinal or primary C–H functionalization, radical relay offers a solution to these long-held problems. Enabled by 1,n (n = 5, 6)-hydrogen atom transfer (HAT), we use a most prevalent moiety, alkene, as the precursor to an sp³ C-centered radical to promote selective cleavage of inert C(sp³)–H bonds for the generation of azidotrifluoromethylated molecules. Mild conditions, broad scope and excellent regioselective control (>20 : 1) are observed in the reactions. Deuterium labelling studies disclose the kinetic characteristics of the transformations and verify a direct 1,n-HAT pathway. The key to this C-centered radical relay is that iron plays a dual role as a radical initiator and terminator to incorporate the azide functionality through radical oxidation via azido–ligand-transfer. The methods and the later derivatization promise expeditious synthesis of CF₃-containing organic azides, γ-lactam and triazoles that are widely used in designing new fluorescent tags and functional materials.

Remote functionalization of inert C(sp³)–H bonds is described via iron-catalyzed sp³ C-centered radical relay.     

Au24和Au25纳米团簇对二氧化碳电化学还原反应催化活性的分析

通过电化学催化过程将二氧化碳(CO2)还原为有用的燃料和化学品是目前降低CO2排放量以及高效利用CO2的主要方式之一.金纳米团簇(Au NCs)因其结构明确、原子级尺寸精确和高表面活性而被认为是CO2电化学还原反应(CO2RR)的良好催化材料和模型催化剂.本研究可控合成了两种金纳米团簇Au24 NCs和Au25 NCs...