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Polyoxometalate-based flexible conductive materials with superionic conductivity

Science China chemistry 2024年第10期67卷 3299-3309页

作者： Yuxin Wang Shuping Xue Jun Geng Ying Lu Teng Li Xiaozheng Duan Xue Bai Yanli Yang Jingqi Yang Shuxia Liu Key Laboratory of Polyoxometalate and Reticular Material chemistry of Ministry of Education College of ChemistryNortheast Normal UniversityChangchun 130024China State Key Laboratory of Polymer Physics and chemistry Changchun Institute of Applied ChemistryChinese Academy of SciencesChangchun 130022China

Flexible ion-conductive materials exhibit intriguing advantages for applications in flexible electronic ***,the further enhancement of their conductivity within environmental limitations is an urgent demand for the development of flexible electronic devices,yet remains as a great ***,we report a“dual-acid”strategy,via the encapsulation of two acids,H_(3)PW_(12)O_(40)(HPW) and NH_(2)SO_(3)H(SA),with synergistic interaction into poly(vinyl alcohol)-glycerol(PVA-Gly) hydrogel,to achieve polyoxometalate(POM)-based flexible materials with superionic conductivity under various environmental *** a representative example,the prepared PVA-Gly/HPW-SA-20% hydrogel presents an ultrahigh proton conductivity ranging from -30℃(3.33×10^(-2)S cm^(-1)) to room temperature(2.78×10^(-1)S cm^(-1)) under ambient ***,the PVA-Gly/HPW-SA-20% hydrogel exhibits remarkable advantages in anti-freezing,mechanical flexibility and self-adhesiveness,making it a promising multifunctional electrolyte for flexible electronic *** experimental results and molecular dynamics(MD) simulations jointly demonstrate that SA bridges HPW clusters to form a dense proton transport pathway induced by multiple electrostatic and hydrogen bonding interactions between SA and HPW counterparts,which contributes to the high-level proton conductivity of the PVA-Gly/HPW-SA-20% *** work provides new insights into the design of POM-based flexible materials with superionic conductivity.

关键词： polyoxometalates proton conduction dual-acid effect hydrogel molecular dynamics simulation

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Tuning microstructures of Mg-Ce-Ni hydrogen storage alloys via Cu and carbon nanotube additions

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Nano Research 2024年第8期17卷 7203-7211页

作者： Linlin Zhang Liang Xiong Bingyang Gao Qingyun Shi Ying Wang Zhiya Han Zhenhua Zhang Chunli Wang Limin Wang Yong Cheng State Key Laboratory of Rare Earth Resource Utilization Changchun Institute of Applied ChemistryChinese Academy of SciencesChangchun 130022China School of applied chemistry and Engineering University of Science and Technology of ChinaHefei 230026China Purification Equipment Research institute of CSIC Handan 056002China

Mg-based alloys are regarded as highly promising materials for hydrogen *** significant improvements of the properties for Mg-based alloys,challenges such as slow hydrogen absorption/desorption kinetics and high thermodynamic stability continue to limit their practical *** this study,to assess hydrogen storage alloys with enhanced properties,incorporating both internal microstructure modulation through the preparation of amorphous/nanocrystalline structures and surface property enhancement with the addition of Cu and carbon nanotubes(CNTs),the kinetic properties of activation and hydrogenation,thermodynamic properties,and dehydrogenation kinetics are *** results reveal a complementary interaction between the added Cu and CNTs,contributing to the superior hydrogen storage performance observed in sample 7A-2Cu-1CNTs with an amorphous/nanocrystalline structure compared to the other experimental ***,the samples are fully activated after the initial hydrogen absorption and desorption cycle,demonstrating outstanding hydrogenation kinetics under both high and low temperature experimental *** noteworthy is that the hydrogen absorption exceeds 1.8 wt.% within one hour at 333 ***,the activation energy for dehydrogenation is decreased to 64.71 kJ·mol^(–1).This research may offer novel insights for the design of new-type Mg-based hydrogen storage alloys,which possess milder conditions for hydrogen absorption and desorption.

关键词： Mg-Ni-Ce alloy hydrogen storage amorphous/nanocrystalline structure kinetics Cu and carbon nanotubes(CNTs)codoping

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Multidimensional regulation of Ti-Zr-Cr-Mn hydrogen storage alloys via Y partial substitution

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Nano Research 2024年第5期17卷 4211-4220页

作者： Haixiang Xiu Wanqiang Liu Dongming Yin Nan Ding Wenfeng Qiao Shaolei Zhao Long Liang Cong Liu Shaohua Wang Qingshuang Wang Bingbing Chen Limin Wang Yong Cheng School of Materials Science and Engineering Changchun University of Science and TechnologyChangchun 130022China State Key Laboratory of Rare Earth Resources Utilization Changchun Institute of Applied ChemistryChinese Academy of Sciences(CAS)Changchun 130022China School of applied chemistry and Engineering University of Science and Technology of ChinaHefei 230026China Department of Energy Science and Engineering Nanjing Tech UniversityNanjing 211816China National Engineering Research Center of Nonferrous Metals Materials and Products for New Energy GRINM Group Co.Ltd.Beijing 100088China GRIMAT Engineering institute Co. Ltd.Beijing 101407China College of Life Science and Technology Changchun University of Science and TechnologyChangchun 130022China

High density and safe storage of hydrogen are the preconditions for the large-scale application of hydrogen ***,the hydrogen storage properties of Ti_(0.6)Zr_(0.4)Cr_(0.6)Mn_(1.4) alloys are systematically studied by introducing Y element instead of Ti element through vacuum arc *** the partial substitution of Y,a second phase of rare earth oxide is added in addition to the main suction hydrogen phase,C14 Laves *** to the unique properties of rare earth elements,the partial substitution of Y can not only improve the activation properties and plateau pressure of the alloys,but also increase the effective hydrogen storage capacity of the *** comprehensive properties of hydrogen storage alloys are improved by multidimensional regulation of rare earth *** them,Ti_(0.552)Y_(0.048)Zr_(0.4)Cr_(0.6)Mn_(1.4) has the best comprehensive *** alloy can absorb hydrogen without activation at room temperature and 5 MPa,with a maximum hydrogen storage capacity of 1.98 wt.%.At the same time,it reduces the stability of the hydride and the enthalpy change value,making it easier to release *** theoretical analysis and first-principle simulation,the results show that the substitution of Y element reduces the migration energy barrier of hydrogen and the structural stability of the system,which is conducive to hydrogen *** alloy has superior durability compared to the original alloy,and the capacity retention rate was 96.79%after 100 hydrogen absorption/desorption cycles.

关键词： AB_(2)-type hydrogen storage alloy rare earth element first-principles simulation multidimensional regulation

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Hollow structured Fe@C nanorods for boosting dehydrogenation properties of α-AlH_(3)

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Nano Research 2024年第9期17卷 8184-8191页

作者： Yuan Zhao Qingshuang Wang Dongming Yin Xiaoli Wang Shouliang Li Chunli Wang Long Liang Shaolei Zhao Limin Wang Yong Cheng School of Materials Science and Engineering Changchun University of Science and TechnologyChangchun 130022China State Key Laboratory of Rare Earth Resource Utilization Changchun Institute of Applied ChemistryChinese Academy of SciencesChangchun 130022China Shandong Provincial Key Laboratory of Monocrystalline Silicon Semiconductor Materials and Technology College of Chemistry and Chemical EngineeringDezhou UniversityDezhou 253023China Henan Nayu New Material Co. Ltd.Xinxiang 453000China

α-AlH_(3)is regarded as one of the most promising hydrogen storage materials due to its high hydrogen storage capacity(10.1 wt.%,148 kg·m^(-3)).However,in practical applications,the associated hydrogen release temperature remains relatively *** effectively address this issue,hollow structured Fe@C nanorods derived from Fe-MOF are introduced as highly efficient catalyst to optimize the dehydrogenation properties ofα-AlH_(3).Comparatively,the initial hydrogen release temperature ofα-AlH_(3)+3 wt.%Fe@C is reduced to 94.2℃,which is significantly lower than that of pureα-AlH_(3)(137.8℃).At 100 and 120℃,it exhibits hydrogen capacities of 5.38 wt.%and 7.47 wt.%,respectively,whereas pureα-AlH_(3)only delivers hydrogen capacities of 0.24 wt.%and 5.94 wt.%under the same *** density functional theory(DFT)calculations further indicate that the existence of Fe@C catalyst can make the length of Al-H bond increase,which is more conducive to the release of *** results show that the synergistic effect of Fe and porous carbon in Fe@C nanorods can improve the hydrogen desorption kinetics ofα-AlH_(3),providing a good prospect for the application ofα-AlH_(3)in hydrogen storage fields.

关键词： Fe@C α-AlH_(3) dehydrogenation catalyst

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模拟宿主防御肽的聚(2-噁唑啉)作为佐剂增强多粘菌素B的抗菌活性并拓展抗菌谱

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Science China Materials 2024年第3期67卷 991-999页

作者：罗政杰赵学斌周敏邹景橙肖希勉刘龙强谢佳洋武月铭张雯静刘润辉 State Key Laboratory of Bioreactor Engineering East China University of Science and TechnologyShanghai 200237China Shanghai Frontiers Science Center of Optogenetic Techniques for Cell Metabolism Key Laboratory for Ultrafine Materials of Ministry of EducationFrontiers Science Center for Materiobiology and Dynamic ChemistryResearch Center for Biomedical Materials of Ministry of EducationSchool of Materials Science and EngineeringEast China University of Science and TechnologyShanghai 200237China Department of Orthopedic Surgery Shanghai General HospitalSchool of MedicineShanghai Jiao Tong UniversityShanghai 200080China

临床上常用的广谱抗生素无法有效解决抗生素高度耐药ESKAPE菌感染的难题,ESKAPE耐药菌已经成为人类生命健康的重大威胁.抗生素与佐剂的联合治疗是解决抗生素耐药菌感染的重要途径,但是探索对所有ESKAPE耐药菌都具有广谱和高效抗菌活性... 详细信息

临床上常用的广谱抗生素无法有效解决抗生素高度耐药ESKAPE菌感染的难题,ESKAPE耐药菌已经成为人类生命健康的重大威胁.抗生素与佐剂的联合治疗是解决抗生素耐药菌感染的重要途径,但是探索对所有ESKAPE耐药菌都具有广谱和高效抗菌活性的抗生素-佐剂组合仍然面临巨大挑战.在这里,我们提出了一种抗生素-佐剂的有效设计策略,将对ESKAPE中耐药阴性菌具有高活性的多粘菌素B(PMB)与模拟宿主防御肽的细菌膜靶向阳离子聚(2-噁唑啉)相结合.我们通过2-噁唑啉单体可控聚合,合成了一系列具有不同疏水性侧链的阳离子聚(2-噁唑啉).研究表明,聚(2-噁唑啉)和PMB的组合效果随着聚(2-噁唑啉)侧链疏水性的提高呈现出从拮抗效应到协同效应的逐渐变化.其中,优选的聚(2-噁唑啉)EACA-POX_(20)显著增强了PMB的抗菌活性,尤其是对于ESKAPE耐药阳性菌的抗菌活性增强了16–32倍.聚(2-噁唑啉)EACA-POX_(20)有效增强了PMB的抗菌活性并扩展了PMB的抗菌谱.聚(2-噁唑啉)和PMB的组合策略能够有效对抗所有耐药ESKAPE病原体,为解决ESKAPE耐药菌提供了新的思路.

关键词： poly(2-oxazoline)s ESKAPE bacteria polymyxin B broad-spectrum activity

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Assay of Histamine in Single Mast Cells by Capillary Zone Electrophoresis with Electrochemical Detection

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chinese Chemical Letters 2002年第10期13卷 982-984页

作者： Qian Feng WENG Fang Quan XIA Wen Rui JIN School of chemistry and Chemical Engineering Shandong UniversityJinan 250100

Capillary zone electrophoresis was employed for the analysis of histamine in single rat peritoneal mast cells using an amperometric detector. In this method, individual mast cells and then 0.02 mol/L NaOH as a lysing solution are injected into the front end of the separation capillary. A cell injector was constructed for easy injection of single cells. Histamine in single mast cells has been identified and quantified.

关键词： Capillary electrophoresis electrochemical detection histamine mast cell.

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Application of Back-propagation Artificial Neural Network in Speciation of Cadmium

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Chemical Research in chinese Universities 2010年第6期26卷 899-904页

作者： WANG Lin-lin ZHANG Jie LIU Hai-yan ZHANG Hai-tao WANG Hong-yan YANG Xiu-rong WANG Ying-hua College of chemistry Jilin University Changchun 130012 P. R. China State Key Laboratory of Electroanalytical chemistry Changchun Institute of Applied Chemistry Chinese Academy of Sciences Changchun 130022 P. R. China

A method for predicting the five species contents of cadmium was developed by combining the back-propagation artificial neural network with graphite furnace atomic absorption spectrometry（BP-ANN-GF-AAS）.Based on the strong learning function and the features of the information distributed storage of artificial neural network（ANN）,a single ANN was constituted in which only one determination point of every sample was *** exchangeable,carbonated,Fe-Mn oxidable,organic and residual species of cadmium for 20 kinds of soil samples from the two sections of changchun（China） were determined by *** detection limit of the method is 0.024 μg/L and the limit of quantification is 0.080 μg/L.t-Test indicates that there is not any systemic error of the results obtained by the Tessier sequential extraction graphite furnace atomic absorption spectrometry method（Tessier-GF-AAS） and *** with those of the Tessier-GF-AAS,the prediction errors of BP-ANN-GF-AAS are less than 10%.The proposed method is fast,convenient,sensitive,and can eliminate the interference among various species.

关键词： Artificial neural network(ANN) Speciation Graphite furnace atomic absorption spectrometry(GF-AAS) Cadmium

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Study on the adsorptive catalytic voltammetry of aloe-emodin at a carbon paste electrode

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Science China chemistry 2005年第5期48卷 442-448页

作者： LI Ju'nan GAO Peng LI Xiangling YAN Zhihong MAO Xun College of chemistry Xiangtan University Xiangtan 411105 China College of Chemistry Xiangtan University Xiangtan 411105 China College of Chemistry Xiangtan University Xiangtan 411105 China College of Chemistry Xiangtan University Xiangtan 411105 China College of Chemistry Xiangtan University Xiangtan 411105 China

A new catalytic voltammetric method for the determination of anthraqunone medi-cines at a carbon paste electrode (CPE) was described for the first time. The mechanism of the catalytic reaction was investigated by using linear sweep voltammetry, cyclic voltammetry, con-stant potential electrolysis and so on. The experiment results indicate that aloe-emodin was effi-ciently accumulated at a CPE by adsorption. In the following potential scan, aloe-emodin was reduced to homologous anthrahydroquinone compound, then the compound was immediately oxidized to aloe-emodin by the dissolved oxygen, and the aloe-emodin was again reduced at the CPE. As a result, a cyclic catalytic reaction was established. But a reversible redox reaction of aloe-emodin can only be observed at a mercury electrode, no catalytic reaction occurs there. A sensitive catalytic voltammetric peak of aloe-emodin was obtained at about ?0.60 V (vs. SCE) in 0.56 mol/L NH3-NH4Cl buffer (pH 8.9). The proposed method was applied to the determination of aloe-emodin in the Radix Rhei with satisfactory results. The determination results were in good agreement with reference values obtained by the HPLC. The adsorptive catalytic voltammetry for the determination of organic compound at CPE, chemically modified electrode and other solid electrodes could be significant in the studies on pharmacology, pharmacodynamics, toxicity of medicine, clinical medicine and biochemistry.

关键词： aloe-emodin, adsorptive catalytic voltammetry, carbon paste electrode.

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Combination of on-line preconcentration by di(2-ethylhexyl) phosphoric acid resin in the presence of complexing agent with microwave plasma-atomic emission spectrometry for the determination of rare earths

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Journal of Rare Earths 2010年第S1期28卷 79-82页

作者：赵晓伟孔祥飞贾琼周伟红曲晓刚 College of chemistry Jilin University Changchu n institute of applied chemistry Chinese Academy of Sciences

The adsorption of rare earths,lanthanum,cerium,neodymium,and yttri um by di(2-ethylhexyl) phosphoric acid(D2EHPA) resin in the presence of a compl exing agent,EDTA,was investigated. Flow injection was selected as the injectin g method. Various parameters,sample pH,sample loading time,sample flow rate,EDTA concentration,EDTA flow rate,eluent concentration,and eluent flow rate,were studied and optimized. Under the optimum conditions,the method allowed the determination of rare earths with detection limits of 1.09 μg/L(lanthanum),3 .31 μg/L(cerium),2.05 μg/L(neodymium),and 1.25 μg/L(yttrium) . High repea tabilities were obtained for all the four rare earths(RSDapplied to the determination of the rare earths in water samples with a recovery range of 95.8%-103.3%.

关键词： di(2-ethylhexyl) phosphoric acid resin complexing agent rare earths

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Structure and electrochemical characteristics of LaNi_5-Ti_(0.10)Zr_(0.16)V_(0.34)Cr_(0.10)Ni_(0.30) composite alloy electrode

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Journal of Rare Earths 2010年第5期28卷 774-780页

作者：王艳芝赵敏寿 College of Environmental and Chemical Engineering Yanshan University State Key Laboratory of Metastable Materials Science and Technology Yanshan University

Composite LaNi5+x wt.% Ti0.10Zr0.16V0.34Cr0.10Ni0.30 (x=0, 1, 5, 10) alloys were prepared by two-step re-melting. X-ray diffractometer (XRD), scanning electron microscopy (FESEM), energy dispersive spectrometry (EDS), inductively coupled plasma (ICP) and electrochemical impedance spectroscopy (EIS) analyses showed that the matrix phase of LaNi5 alloy with CaCu5 structure remained unchanged after additive alloy was added, the amount of the second phase increased with increasing x. The synergetic effect withi...

关键词： Ni/MH battery metal hydride electrode composite alloy electrochemical properties kinetic properties rare earths

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