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Electrodeposition of nickel hydroxide nanoparticles on carbon nanotube electrodes : correlation of particle crystallography with electrocatalytic properties

机译:碳纳米管电极上氢氧化镍纳米粒子的电沉积:粒子晶体学与电催化性能的关系

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摘要

The use of two different electrodeposition approaches to form nickel hydroxide, Ni(OH)2, nanoparticles (NPs) of different crystallographic orientations on single-walled carbon nanotubes is demonstrated via: (i) the electrochemical generation of OH– (∼mM), in the presence of Ni2+, resulting in the formation of disordered α-phase Ni(OH)2 NPs by precipitation (direct approach); (ii) the electrodeposition of Ni NPs that are converted to Ni(OH)2 through potential cycling in alkaline media to form the more thermodynamically favorable, ordered β-phase Ni(OH)2 NPs (indirect approach). NPs produced by the direct approach exhibit remarkable electrocatalytic activity toward both methanol and ethanol oxidation, with excellent specific activities (SAs) of ∼2.8 kA g–1 for 0.5 M methanol and ∼3.7 kA g–1 for 0.5 M ethanol. In contrast, NPs produced by the indirect approach show SA values about an order of magnitude lower. This study demonstrates the capability of electrochemistry for the tailored synthesis of Ni(OH)2 nanostructures for electrocatalytic applications and a powerful, but simple, combinatorial approach for quick activity screening.
机译:通过以下两种方法证明了使用两种不同的电沉积方法在单壁碳纳米管上形成具有不同晶体学取向的氢氧化镍Ni(OH)2,纳米颗粒(NPs):(i)电化学生成OH-(〜mM),在存在Ni2 +的情况下,通过沉淀形成无序的α相Ni(OH)2 NP(直接方法); (ii)在碱性介质中通过电势循环转化为Ni(OH)2的Ni NPs的电沉积,以形成热力学上更有利的有序β相Ni(OH)2 NPs(间接方法)。通过直接方法生产的NP对甲醇和乙醇氧化均显示出显着的电催化活性,对于0.5 M的甲醇具有约2.8 kA g–1的出色比活度(SA),对于0.5 M的乙醇具有约3.7 kA g-1的出色的比活性。相反,通过间接方法产生的NP显示出的SA值大约低一个数量级。这项研究证明了电化学用于定制Ni(OH)2纳米结构用于电催化应用的能力,以及一种功能强大但简单的组合方法以进行快速活性筛选。

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