Bimetallic Covalent Organic Frameworks for Constructing Multifunctional Electrocatalyst

Covalent organic frameworks (COFs) are a new class of crystalline porous polymers comprised mainly of carbon atoms, and are versatile for the integration of heteroatoms such as B, O, and N into the skeletons. The designable structure and abundant composition render COFs useful as precursors for heteroatom-doped porous carbons for energy storage and conversion. Herein, we describe a multifunctional electrochemical catalyst obtained through pyrolysis of a bimetallic COF. The catalyst possesses hierarchical pores and abundant iron and cobalt nanoparticles embedded with standing carbon layers. By integrating these features, the catalyst exhibits excellent electrochemical catalytic activity in the oxygen reduction reaction (ORR), with a 50 mV positive half-wave potential, a higher limited diffusion current density, and a much smaller Tafel slope than a Pt-C catalyst. Moreover, the catalyst displays superior electrochemical performance toward the hydrogen evolution reaction (HER), with overpotentials of −0.26 V and −0.33 V in acidic and alkaline aqueous solution, respectively, at a current density of 10 mA cm⁻². The overpotential in the catalysis of the oxygen evolution reaction (OER) was 1.59 V at the same current density.     

A New Family of Cyclic Difference Sets with Singer Parameters in Characteristic Three

We construct a new family of cyclic difference sets with parameters ((3 ^d – 1)/2, (3 ^{d – 1} – 1)/2, (3 ^{d – 2} – 1)/2) for each odd d. The difference sets are constructed with certain maps that form Jacobi sums. These new difference sets are similar to Maschietti's hyperoval difference sets, of the Segre type, in characteristic two. We conclude by calculating the 3-ranks of the new difference sets.     

Rhythmic pattern formations in gels and Matalon—Packter law: A fresh perspective

The periodic precipitation pattern formation in gelatinous media is interpreted as a moving boundary problem. The time law, spacing law and width law are revisited on the basis of the new scenario. The explicit dependence of the geometric structure on the initial concentrations of the reactants is derived. Matalon—Packter law, which relates the spacing coefficient with the initial concentrations is reformulated removing many ambiguities and impractical parameters. Experimental results are discussed to establish the significance of moving boundary concept in the diffusion controlled pattern forming systems     

On co-semihereditary rings

A ringR is left co-semihereditary (strongly left co-semihereditary) if every finitely cogenerated factor of a finitely cogenerated (arbitrary) injective leftR-module is injective. A left co-semihereditary ring, which is not strongly left co-semihereditary, is given to answer a question of Miller and Tumidge in the negative. If _R U _S defines a Morita duality,R is proved to be left co-semihereditary (left semihereditmy) if and only ifS is right semihereditary (right co-semihereditary). Assuming thatS⩾R is an almost excellent extension,S is shown to be (strongly) right co-semihereditary if and only ifR is (strongly) right co-semihereditary. Project supported by the National Natural Science Foundation of China.     

一类最高权向量环的Krull维数

本文给出Om×GLn作用于Cm,n上的复多项式环上的最高权向量环的Krull维数公式,从而改正了Aslaksen,Tan及Zhu的一个错误.     

Direct mass measurements of neutron-deficient 152Sm projectile fragments at the FRS-ESR facility

The FRS-ESR facility at GSI provides one of the most efficient methods for direct mass measurements. In the present experiment, exotic nuclei were produced via fragmentation of ¹⁵²Sm projectiles in a thick beryllium target at 500-600 MeV/u, separated in-flight with the fragment separator FRS, and injected into the storage-cooler ring ESR. Time-resolved Schottky Mass Spectrometry was applied for mass measurements of stored and electron-cooled bare and few-electron ions. 373 different nuclides were identified by means of the spectra of their revolution frequencies. Masses for 18 nuclides (⁸⁴Zr, ⁹²Ru, ⁹⁴Rh, ^107,108,110Sb, ^111,112,114I, ¹¹⁸Ba, ^122,123La, ¹²⁴Ce, ¹²⁷Pr, ¹²⁹Nd, ¹³²Pm, ¹³⁴Sm, ¹³⁷Eu) have been determined for the first time. Masses for ^111,112I and ¹¹³Xe have been obtained via known α-decay energies. The experiment and first results will be presented.     

有限局部环Z/2\+kZ上斜对称矩阵标准形和伪辛群的阶

设R=Z/2\+kZ(k>1)是\{2\}[TX-]为非单位的有限局部环. 该文首先确定了R上斜对称矩阵标准形. 设G\+m\-p(R,H)={P∈GL\-m(R)|PHP′=H}是由矩阵H确定的伪辛群,其中H=[JB((][HL(2]0[]I\+\{(v)\}\=-I\+\{(v)\}[]0[HL)][JB))]Δ，Δ=[JB((][HL(2]\{2\}[TX-]\+\{k-1\}[]\{1\}[TX-]\=-\{1\}[TX-][]0[HL)][JB))]. 其次,计算了伪辛群G\+m\-P(R,H)的阶|G\+m\-P(R,H)|.