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Mesophase micelle-assisted electrodeposition and magnetisation behavior of meso-porous nickel films for efficient electrochemical energy and magnetic device applications

机译:介孔胶束辅助的介孔镍膜电沉积和磁化行为,用于高效的电化学能量和磁性装置应用

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Mesoporous magnetic materials have found interesting potential applications in electrochemical energy harvesting and energy-efficient magnetic actuation device applications. Here we report on the electrodeposition and magnetic properties of mesoporous nickel films from lyotropic liquid crystal (LLC) templates formed by cetyltrimethylammoniumbromide (CTAB) cationic surfactant. Diffusion-controlled electrodeposition mechanism of nickel is determined. Films are electrodeposited under a constant current ranging from 1 to 7.5 mA cm(-2) from an aqueous solution containing 0.1 M nickel sulphate, 0.2 M boric acid solution and CTAB with a concentration ranging from 0 to 50 wt.%. Mesopores develop an arranged hexagonal structure due to the micellar positional and orientational order reaching its highest value at 30 wt.% of CTAB at 2 mA cm(-2). This is confirmed by transmission electron microscopy (TEM) and electrocatalytic surface area measurement. Electrodeposition current density and pH modify the mesoporous dimensions and therefore the magnetic properties change, tough hydrogen evolution as a side reaction influences the mesoporous structure. We observe an increased in-plane magnetic coercivity value to a maximum of 214 Oe for the mesoporous nickel film, which correlates with the increased interaction field. The widening of the coercivity distribution in first-order reversal curve (FORC) diagrams indicates that films with higher CTAB content have more inhomogeneous structure, which can lead to complex magnetization reversal mechanisms. The results of this study will help to exploit novel multifunctional magnetic and electrochemical energy materials and devices.
机译:中孔磁性材料在电化学能量收集和节能型磁致动装置应用中发现了有趣的潜在应用。在这里,我们报告了由十六烷基三甲基溴化铵(CTAB)阳离子表面活性剂形成的溶致液晶(LLC)模板中孔镍膜的电沉积和磁性。确定了镍的扩散控制电沉积机理。在浓度范围为0至50 wt。%的含有0.1 M硫酸镍,0.2 M硼酸溶液和CTAB的水溶液中,在1至7.5 mA cm(-2)的恒定电流下对膜进行电沉积。中孔由于胶束的位置和取向顺序在2 mA cm(-2)处CTAB的30 wt。%达到最高值而形成了排列的六边形结构。这通过透射电子显微镜(TEM)和电催化表面积测量得到证实。电沉积电流密度和pH值会改变介孔尺寸,因此磁性会发生变化,由于副反应而产生的大量氢会影响介孔结构。我们观察到中孔镍膜的平面内矫顽力值增加到最大值214 Oe,这与增加的相互作用场有关。一阶反转曲线(FORC)图中矫顽力分布的加宽表明,CTAB含量较高的薄膜结构更不均匀,这可能导致复杂的磁化反转机理。这项研究的结果将有助于开发新型的多功能磁和电化学能材料和器件。

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