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31.
N,N-二甲基甲酰胺中电沉积制备镁镍储氢合金   总被引:1,自引:0,他引:1  
张晓燕  刘卫红 《化学学报》2007,65(7):575-578
采用恒电位沉积法, 选用适宜的添加剂和络合剂, 成功地从N,N-二甲基甲酰胺(DMF)中沉积出致密的黑色Mg-Ni储氢合金膜. 并初步探讨了其共沉积机理. XRD显示沉积层中含有非晶态Mg-Ni相和微晶态Mg相. SEM图及相应能谱图分析表明合金颗粒以团聚状态存在, 合金成分不是很均匀. AAS分析表明沉积合金中Mg的原子摩尔分数达27.3%. LAND电池测试系统测得所镀合金膜的放电比容量最高为172.4 mAh/g.  相似文献   
32.
采用傅立叶变换红外光谱分析了2A12-T6铝合金表面自组装双-(!-三乙氧基硅丙基)四硫化物硅烷偶联剂(SCA)薄膜结构特征,并采用电化学极化曲线评价了薄膜的耐蚀性能.结果表明,铝材表面自然晾干,SCA薄膜分子之间主要通过氢键连接,腐蚀电流密度减小1个数量级以上.120℃的加热处理促进铝板表面通过SiOSi链接而形成SCA网状薄膜结构,并通过在界面上形成SiOAl界面相结构而与铝板表面牢固连接,腐蚀电流密度降低2个数量级以上.SCA乙醇溶液浸泡处理10min比浸泡2s~1min的铝板表面SCA薄膜内氢键缔合羟基要多.  相似文献   
33.
The kinetics of the nucleation and growth of PbO2 during the potentiostatic oxidation of PbSO4 in a lead anodic film was studied using linear sweep voltammetry, potential-step and ac impedance tracing methods. The film investigated is the partially reduced anodic PbO2 film formed by polarizing a lead electrode in 4.5 M H2SO4 solution first at 1.3 V vs. Hg|HgSO4 for 20 min and then at 0.9 V for 5 min. The nucleation and growth process begins some time after the potential step and is completed within 60 s. The pre- and post-nucleation and growth processes correspond to the growth of the anodic film formed by the oxidation of the lead substrate. The mathematical equations representing the current-time and capacitance-time transients are derived taking the background oxidation current into account. The experimental results are well fitted by these equations. The process obeys the laws of two-dimensional instantaneous nucleation and growth.  相似文献   
34.
The kinetics of a multistep reaction of electrodeposition of iron out of aqueous citrate-containing solutions of trivalent iron is investigated. It is shown that concentrations of major solution components affect the partial current density of discharge of ions of divalent iron. It is established that the deposition of metallic iron occurs as a result of discharge of intermediates, which are hydroxy complexes of divalent iron. Kinetic parameters and mechanism of the reaction of discharge of complexes [FeOH]+ to a metallic state are determined. It is mentioned that the formation of poorly soluble hydroxy compounds of trivalent iron in a near-electrode layer leads to a decrease in the iron deposition current.  相似文献   
35.
《Electroanalysis》2006,18(12):1202-1207
A new type of current sensor, Langmuir–Blodgett (LB) film of calixarene on the surface of glassy carbon electrode (GCE) was prepared for determination of mercury by anodic stripping voltammetry (ASV). An anodic stripping peak was obtained at 0.15 V (vs. SCE) by scanning the potential from ?0.6 to +0.6 V. Compared with a bare GCE, the LB film coated electrode greatly improves the sensitivity of measuring mercury ion. The fabricated electrode in a 0.1 M H2SO4+0.01 M HCl solution shows a linear voltammetric response in the range of 0.07–40 μg L?1 and detection limit of 0.04 μg L?1 (ca. 2×10?10 M). The high sensitivity, selectivity, and stability of this LB film modified electrode demonstrates its practical application for a simple, rapid and economical determination of Hg2+ in a water sample.  相似文献   
36.
A free standing film of polyaniline as large as 18 cm×18cm×0.002 cm can be obtained by evaporation of a solution of the chemically synthesized base in NMP. Its structure was examined by the elemental analysis, IR, U.V.-visible spectra, XPS, DSC, SEM and X-ray scattering and its conducting behavior as well as electrochemical properties were studied. Results show that the composition, structure of main chain, physical properties of the free standing film of polyanilme is similar to that of the powder. However, some differences in its electronic structure, conductivity at room temperature and potential of redox couple between the flee standing film and powder are observed, which may be due to cross-linking of the film of polyaniline.  相似文献   
37.
A new type of carbon paste electrode modified with clay mineral and covered with a mercury film is presented in this work. Electrodeposition of the mercury film was performed on the carbon paste electrode modified with montmorillonite. The mercury film was deposited by both electrodeposition in situ and a preliminary electrodeposition. The pre-deposited film of mercury showed to be suitable for anodic stripping voltammetry. An open-circuit sorption of Cd, Pb, and Cu with subsequent anodic stripping voltammetry exhibited higher current responses of metals. Besides the enhanced sensitivity superior separation of the current responses during a simultaneous stripping of metals is expected to be achieved by means of the newly prepared electrode. Presented at the 57th Congress of Chemical Societies, Tatranské Matliare, 4–8 September 2005.  相似文献   
38.
不同取向的CoSb3纳米线阵列的电化学法制备   总被引:1,自引:0,他引:1       下载免费PDF全文
近年来,金属纳米线及其阵列由于其新奇的物理和化学特性和在纳米器件方面潜在的应用前景,越来越受到人们的关注。氧化铝模板合成一维纳米材料具有设备简单、制作方便等优点,因而成为近年来人们常用的一种方法。利用电化学沉积的方法在多孔氧化铝模板中沉积各种成分的纳米线已成为纳米材料制备的一种常见的方法。这种方法不仅可以得到大面积有序的纳米线阵列,还可以根据需要调节孔洞的大小来控制纳米线的直径[1 ̄3]。最近理论研究结果预言[4 ̄6],由于纳米材料的量子限域效应,热电材料的纳米线将有比其相应块体材料更高的品质因数n,这极大地激…  相似文献   
39.
Herein, we demonstrate that silica films with perpendicular macroporous channels and accessible ordered mesopores can be conveniently prepared. The hierarchical macroporous–mesoporous silica films are synthesized by using zinc oxide nanorod array as macroporous template and CTAB surfactant as mesoporous template. In basic surfactant-containing solution, ordered mesoporous silica shells homogeneously grow on the zinc oxide nanorod array. The growth of the mesostructures do not require any chemical modification for the zinc oxide nanorod, which opens a new way for preparing hierarchical silica films with perpendicular mesochannels. The prepared hierarchical macroporous–mesoporous silica films possess a uniform thickness of 2 mm, large perpendicular macropores with a length of 1.8 mm and a width of 80 nm, and accessible ordered mesopores. Separation experiment demonstrates that this macroporous–mesoporous film can effectively separate biomolecules with different sizes.  相似文献   
40.
Porous anodic alumina (PAA) was used as a template to prepare Co nanowires array from 1-ethyl-3-methylimidazolium chloride ionic liquid by direct current method. The surface morphology of porous anodic alumina template was observed by field emission-scanning tunneling microscopy (FE-SEM) before and after the electrodeposition of Co nanowires. The electrodeposition of Co nanowires was characterized by transmission electron microscopy (TEM) and X-ray powder diffraction (XRD). TEM results indicate that the Co nanowire surface is coarse and porous when aqueous solution was used as electrolyte, and the Co nanowire deposited from the ionic liquid is uniform and smooth. XRD results show that the electrodeposition of Co is a mixture of crystal and microcrystal phase.  相似文献   
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