Ni2P Interlayer and Mn Doping Synergistically Expedite the Hydrogen Evolution Reaction Kinetics of Co2P

Transition metal phosphide is regarded as one of the most promising candidates to replace noble-metal hydrogen evolution reaction (HER) electrocatalysts. Nevertheless, the controllable design and synthesis of transition metal phosphide electrocatalysts with efficient and stable electrochemical performance are still very challenging. Herein, a novel hierarchical HER electrocatalyst consisting of three-dimensional (3D) coral-like Mn-doped Co₂P@an intermediate layer of Ni₂P generated in situ by phosphorization on Ni foam (MnCoP/NiP/NF) is reported. Notably, both the incorporation of Mn and introduction of the Ni₂P interlayer promote Co atoms to carry more electrons, which is beneficial to reduce the force of the Co−H bond and optimize the adsorption energy of hydrogen intermediate (|ΔG_H*|), thereby making MnCoP/NiP/NF exhibit outstanding HER performance with onset overpotential and Tafel slope as low as 31.2 mV and 61 mV dec⁻¹, respectively, in 1 m KOH electrolyte.     

Interfacial Sites in Ag Supported Layered Double Oxide for Dehydrogenation Coupling of Ethanol to n-Butanol

Upgrading of ethanol to n-butanol through dehydrogenation coupling has received increasing attention due to the wide application of n-butanol. But the enhancement of ethanol dehydrogenation and followed coupling to produce high selectivity to n-butanol is still highly desired. Our previous work has reported an acid-base-Ag synergistic catalysis, with Ag particles supported on Mg and Al-containing layered double oxides (Ag/MgAl-LDO). Here, Ag-LDO interfaces have been manipulated for dehydrogenation coupling of ethanol to n-butanol by tailoring the size of Ag particles and the interactions between Ag and LDO. It has been revealed that increasing the population of surface Ag sites at Ag-LDO interfaces promotes not only the dehydrogenation of ethanol to acetaldehyde but also the subsequent aldol condensation of generated acetaldehyde. A selectivity of up to 76 % to n-butanol with an ethanol conversion of 44 % has been achieved on Ag/LDO with abundant interfacial Ag sites, much superior to the state-of-the-art catalysts.     

Representation type of endomorphism algebras of exceptional sequences of typeA n

LetF be an algebraically closed field, be a quiver of typeA _n . In this paper we prove that the endomorphism algebras of exceptional sequences over are sums of finitely many tilted algebras of typeA _m wherem≤n by using perpendicular categories, and thus the endomorphism algebras of exceptional sequences of typeA _n are representation-finite. Supported by Chinese Postdoctorate Fund and Beijing Youth Fund     

精准微创个体化医疗、3D打印及计算机导航技术在骨科临床的研究进展

随着近年来3D打印、有限元分析及计算机导航技术迅速发展, 为智能精准微创个体化医疗尤其是骨科临床应用提供了路径和方法. 本文首先对当前精准微创的个性化医疗发展趋势, 以及3D打印和有限元分析在骨科的临床应用进行介绍, 并详细探讨了计算机导航技术在骨科中的临床应用价值和存在的不足, 最后对未来3D打印和骨科计算机导航技术的发展趋势进行了展望.     

基于2D Chebyshev-Sine映射的图像加密算法

混沌系统因对初始条件和参数具有极度的敏感性、遍历性和不可预测性,被广泛应用于图像加密领域。提出了一种二维映射——二维Chebyshev-Sine映射。通过分析轨迹图得到映射,与其他混沌映射相比,此映射拥有更宽广的混沌范围和良好的遍历性,对初始条件和系统参数具有高度敏感性,实现成本相对较低。基于此,提出了一种线性混合层图像加密算法:通过行移位和列混合有效改变图像像素空间位置和像素频域中的值,同时使用了中国剩余定理的扩散原则。实验仿真结果证明,此加密算法具有抵抗差分攻击和选择明文攻击的性能,且运行速度快,安全性较高。     

Condition for invariant spectral degree of coherence of an electromagnetic plane wave on scattering

Within the accuracy of the first-order Born approximation, the condition for invariant spectral degree of coherence of an electromagnetic plane wave scattered from random media is presented. The condition for the electromagnetic plane wave is different from the one for the scalar plane wave. Results also indicate that, different polarizations of the incident plane wave would have essential effects on analytical forms of the condition. These effects may be due to the correlation-induced changes in the scattered spectral degree of coherence.     

Three fabricated pigments (Han purple,indigo and emerald green) in ancient Chinese artifacts studied by Raman microscopy,energy‐dispersive X‐ray spectrometry and polarized light microscopy

In this study, we analyzed three fabricated pigments from ancient artifacts in China. The purple pigment was obtained from a painted pottery figurine unearthed from the Chu Tombs group of the Western Han dynasty in Xuzhou, Jiangsu Province. The dark blue dye was from silk textiles in the Palace Museum. The green pigment was from decorative paintings on ancient architectures in the Palace Museum. These pigments were analyzed with Raman microscopy (RM), energy‐dispersive X‐ray (EDX) analytic spectroscopy and polarized light microscopy (PLM). By comparing their Raman spectra with standard samples, the primary ingredients of the purple pigment and the dark blue dye were found to be Han purple and indigo, respectively. However, the green pigment could not be identified by RM because of strong fluorescence. It was then confirmed to be emerald green by using EDX analytic microscopy and PLM. We also describe the traditional manufacturing methods of these pigments and their applications on artifacts in Chinese history. Copyright © 2007 John Wiley & Sons, Ltd.     

Simultaneous determination of bioactive flavone derivatives in Chinese herb extraction by capillary electrophoresis used different electrolyte systems--borate and ionic liquids

In this paper, novel capillary electrophoresis (CE) methods, which used ionic liquids (1-ethyl-3-methylimidazoium tetrafluoroborate, 1-butyl-3-methylimidazoium tetrafluoroborate), were established to separate and determine some bioactive flavone derivatives in Chinese herb Seriphidium santolinum (Schrenk) Poljak. In order to investigate the traits of ionic liquids in CE, borate was also used as electrolyte to compare with. And the excellence of CE, which used ionic liquids as main running electrolyte and beta-cyclodextrin (beta-CD) as modifier, was illuminated as well. As a result of the study, the difference of ionic liquids and borate in CE was discussed and the advantage of CE, which used ionic liquids as electrolytes for separation, was shown. The analysis was obtained within short time (5-6 min). From the result, it was found that the system, which used ionic liquids, was robust because the joule heating was small. The method of CE, which used ionic liquids, has lower detection limits (0.137-0.642 microg/mL) than that of borate (0.762-1.036 microg/mL). And the CE, which used ionic liquids method, has lower limit of linear range (1.100-2.656 microg/mL), while that of CE, which used borate method, was 2.188-5.313 microg/mL.     

Structure Engineering of BiSbSx Nanocrystals Embedded within Sulfurized Polyacrylonitrile Fibers for High Performance of Potassium-Ion Batteries

Potassium-ion batteries (PIBs) are regarded as promising candidates in next-generation energy storage technology; however, the electrode materials in PIBs are usually restricted by the shortcomings of large volume expansion and poor cycling stability stemming from a high resistance towards diffusion and insertion of large-sized K ions. In this study, BiSbS_x nanocrystals are rationally integrated with sulfurized polyacrylonitrile (SPAN) fibres through electrospinning technology with an annealing process. Such a unique structure, in which BiSbS_x nanocrystals are embedded inside the SPAN fibre, affords multiple binding sites and a short diffusion length for K⁺ to realize fast kinetics. In addition, the molecular structure of SPAN features robust chemical interactions for stationary diffluent discharge products. Thus, the electrode demonstrates a superior potassium storage performance with an excellent reversible capacity of 790 mAh g⁻¹ (at 0.1 A g⁻¹ after 50 cycles) and 472 mAh g⁻¹ (at 1 A g⁻¹ after 2000 cycles). It's one of the best performances for metal dichalcogenides anodes for PIBs to date. The unusual performance of the BiSbS_x@SPAN composite is attributed to the synergistic effects of the judicious nanostructure engineering of BiSbS_x nanocrystals as well as the chemical interaction and confinement of SPAN fibers.     

Photo-thermal Cooperative Carbonylation of Ethanol with CO2 on Cu2O-SrTiCuO3-x

Carbonylation of ethanol with CO₂ as carbonyl source into value-added esters is of considerable significance and interest, while remains of great challenge due to the harsh conditions for activation of inert CO₂ in that the harsh conditions result in undesired activation of α-C−H and even cleavage of C−C bond in ethanol to deteriorate the specific activation of O−H bond. Herein, we propose a photo-thermal cooperative strategy for carbonylation of ethanol with CO₂, in which CO₂ is activated to reactive CO via photo-catalysis with the assistance of *H from thermally-catalyzed dissociation of alcoholic O−H bond. To achieve this proposal, an interfacial site and oxygen vacancy both abundant SrTiCuO_3-x supported Cu₂O (Cu₂O-SrTiCuO_3-x) has been designed. A production of up to 320 μmol g⁻¹ h⁻¹ for ethyl formate with a selectivity of 85.6 % to targeted alcoholic O−H activation has been afforded in photo-thermal assisted gas-solid process under 3.29 W cm⁻¹ of UV/Vis light irradiation (144 °C) and 0.2 MPa CO₂. In the photo-driven activation of CO₂ and following carbonylation, CO₂ activation energy decreases to 12.6 kJ mol⁻¹, and the cleavage of alcoholic α-C−H bond has been suppressed.