Darboux transformation and exact multisolitons for a matrix coupled dispersionless system

We present a matrix coupled dispersionless(CD) system. A Lax pair for the matrix CD system is proposed and Darboux transformation is constructed on the solutions of the matrix CD system and the associated Lax pair. We express an N soliton formula for the solutions of the matrix CD system in terms of quasideterminants. By using properties of the quasideterminants, we obtain some exact solutions, including bright and dark-type solitons, rogue wave and breather solutions of the matrix CD system. Furthermore, it has been shown that the solutions of the matrix CD system are expressed in terms of solutions to the usual CD system, sine-Gordon equation and Maxwell-Bloch system.     

第三族金属氧化物离子对二氧化碳转化的红外光谱研究

本文利用红外光解离光谱研究了第三族金属氧化物离子对二氧化碳分子的转化机制. 研究表明，对于[ScO(CO₂)_n]⁺体系，在n≤4时，形成了溶剂化结构；在n=5时，形成了碳酸盐结构，实现了二氧化碳的转化. 对于[YO(CO₂)_n]⁺体系，需要4个二氧化碳分子就可以实现二氧化碳的转化. 而在[YO(CO₂)_n]⁺体系中，只发现了溶剂化结构，没有观察到碳酸盐结构. 理论计算表明，[YO(CO₂)_n]⁺体系拥有最小的溶剂化结构向碳酸盐结构转化能垒，[LaO(CO₂)_n]⁺体系拥有最大的溶剂化结构向碳酸盐结构转化能垒. 本文从分子水平揭示了不同金属氧化物离子对二氧化碳分子转化的影响规律.     

若干高维可积和不可积模型的严格解

可积和不可积模型可以描述自然科学中的诸多现象, 寻找高维非线性模型的严格解已成为可积系统的一个重要研究内容. 结合达布变换法和多线性分离变量法, 可以得到多个(2+1)维非线性模型包含任意函数的严格解, 通过选取不同的任意函数, 构造这些非线性模型新的相互激发模式. 进一步推广了形变映射理论, 建立了变系数 场和sine-Gordon以及双sine-Gordon场的形变映射关系, 从而得到高维不可积模型包含任意函数的新严格解. 对任意函数的不同选择, 构造了sine-Gordon和双sine-Gordon可积模型丰富的局域解和周期解, 如多solitoff解及其周期波推广、周期形变的蛇形孤波解以及变模的拟周期解等.     

Multi-phase transformation kinetics of HSLA steels during continuous cooling: experiments and cellular automaton (CA) simulation

ABSTRACT

Kinetics of multiply ferrite/bainite phase transformation of HSLA steels is investigated by experiments and cellular automaton (CA) simulation. Peak-differentiation method to elucidate the sequential ferrite and bainite phase transformation individually, which is verified by the CA simulation. Such CA modelling executed using classic JMAK theory, but also gives an insight of microstructure evolution of the multi-phase transformation routine on different cooling rate. From that, it enables classic JMAK modelling to capture the detached phase transformation with different growth models and interface-migration mechanisms. Also, we find that the final phase constitution is sensitive to the cooling rate. With increasing the cooling rate, bainite sheaves nucleated at prior austenite boundaries and ferrite/austenite interfaces are significantly facilitated, which seriously inhibits the growth of prior ferrites. The scenario can be interpreted by the CA simulation and the influence of the cooling rate on sequential multi-phase transformation can be also obtained.     

无溶剂热处理固相转化法简易制备沸石咪唑酯骨架材料

设计开发了一种无需溶剂，通过热处理固相转化制备沸石咪唑酯骨架材料（ZIFs）的简易方法.该方法无需溶剂及其它预处理，只需将金属源与有机配体固相混合后于低温（200℃）热处理即可实现多孔晶体材料的制备.所合成材料H-ZIF-67为具有方纳石拓扑结构的纳米晶体，与传统方式合成的ZIFs材料一致.粉末X射线衍射（PXRD）分析结果表明产物的晶体结构与标准ZIFs谱图一致.通过扫描电子显微镜（SEM）、透射电子显微镜（TEM）、N₂吸附-脱附分析、热重分析（TGA）和傅里叶变换红外光谱（FTIR）等手段对合成的材料进行了表征，发现H-ZIF-67材料具有与ZIFs材料类似的特性.该方法经济、高效，摒弃了传统方法合成ZIFs材料周期长、处理过程复杂的弊端，为ZIFs材料的量产提供了新思路.     

X-ray Crystallographic Observation of Chiral Transformations within a Metal–Peptide Pore

Porous metal complexes enable single-crystal X-ray crystallographic observation of included guests or reaction intermediates through simple soaking with the guests/substrates. Previous studies on this technique have often encountered difficulties in the observation of chiral structures because the host frameworks had no chirality. We synthesized a new metal–peptide porous complex through a folding-and-assembly strategy and utilized the chiral pore for trapping chiral guests. Chiral alcohols and ketones were successfully included within the pore. Crystallographic analyses clearly revealed not only their chemical structures but also chiral transformation events within the pore such as fixed conformations or an unstable hemiacetal formation.     

Tuning Electrical- and Photo-Conductivity by Cation Exchange within a Redox-Active Tetrathiafulvalene-Based Metal–Organic Framework

To activate electronic and optical functions of the redox-active metal–organic framework, (Me₂NH₂)[In^III(TTFTB)]⋅0.7 C₂H₅OH⋅DMF (Me₂NH₂@ 1 , TTFTB=tetrathiafulvalene-tetrabenzoate, DMF=N,N-dimethylformamide), has been exchanged by tetrathiafulvalenium (TTF^.+) and N,N′-dimethyl-4,4′-bipyridinium (MV²⁺). These cations provide electron carriers and photosensitivity. The exchange retains the crystallinity allowing single-crystal to single-crystal post-synthetic transformation to TTF@ 1 and MV@ 1 . Both TTF^.+ and MV²⁺ enhance the electrical conductivity by a factor of 10² and the visible light induced photocurrent by 4 and 28 times, respectively. EPR evidences synergetic effect involving charge transfer between the framework redox-active TTFTB bridges and MV²⁺. The results demonstrate that functionalization of MOF by cation exchange without perturbing the crystallinity extends possibilities to achieve switchable materials.     

Adaptive Bifunctional Electrocatalyst of Amorphous CoFe Oxide @ 2D Black Phosphorus for Overall Water Splitting

Water electrolysis offers a promising green technology to tackle the global energy and environmental crisis, but its efficiency is greatly limited by the sluggish reaction kinetics of both the cathodic hydrogen evolution reaction (HER) and anodic oxygen evolution reaction (OER). In this work, by growing amorphous multi-transition-metal (cobalt and iron) oxide on two-dimensional (2D) black phosphorus (BP), we develop a bifunctional electrocatalyst (CoFeO@BP), which is able to efficiently catalyze both HER and OER. The overpotentials for the hybrid CoFeO@BP catalyst to reach a current density of 10 mA cm⁻² in 1 m KOH are 88 and 266 mV for HER and OER, respectively. Based on a series of ex-situ and in situ investigations, the excellent catalytic performance of CoFeO@BP is found to result from the adaptive surface structure under reduction and oxidation potentials. CoFeO@BP can be transformed to CoFe phosphide under reduction potential, in situ generating the real active catalyst for HER.