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Nanoscale Ni-B Electrocatalyst Prepared from Nickel Ethylenediamine Complex for Direct Ethanol Electrocatalytic Oxidation

机译:乙二胺镍络合物制备的纳米Ni-B电催化剂用于乙醇直接电催化氧化

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摘要

Ni-B/Cu electrode prepared by the electroless deposition technique of chemical reduction of nickel ethylenediamine complex with BH_4~- was characterized by SEM, XRD and XPS techniques, respectively, and evaluated using ethanol electrocatalytic oxidation by the method of cyclic voltammetry. The as-prepared Ni-B/Cu electrode exhibited much higher electrocatalytic activity than the Ni-B/Cu electrode obtained via direct reduction of nickel metallic ions. The effects of the nickel ethylene-diamine complex can be attributed to both the structural effect and electronic effect. The nickel ethylenediamine complex can not only make an electroless deposition stable and highly dispersed, but also facilitate the formation of more nanoscale microcrystalline Ni on the electrode surface, which increased the electrochemical oxidation activity. Moreover, ethylenediamine influenced the electronic states of Ni and B on the electrode surface, more electrons transfer from the B to Ni that the Ni active sites became more highly unsaturated, which could promote the form of adsorbed active ethanol.
机译:采用SEM,XRD和XPS技术分别表征了以BH_4〜-对乙二胺镍配合物进行化学还原的化学沉积技术制备的Ni-B / Cu电极,并通过循环伏安法采用乙醇电催化氧化法对其进行了评价。所制备的Ni-B / Cu电极表现出比通过直接还原镍金属离子获得的Ni-B / Cu电极高得多的电催化活性。乙撑二胺镍配合物的作用可归因于结构作用和电子作用。乙二胺镍配合物不仅可以使化学沉积稳定且高度分散,还有助于在电极表面形成更多纳米级的微晶Ni,从而提高了电化学氧化活性。此外,乙二胺影响电极表面Ni和B的电子态,更多的电子从B转移到Ni,Ni活性位变得更加高度不饱和,这可能促进吸附的活性乙醇的形成。

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