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Anion insertion enhanced electrodeposition of robust metal hydroxide/oxide electrodes for oxygen evolution

机译:阴离子插入增强了用于析氧的坚固金属氢氧化物/氧化物电极的电沉积

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Electrochemical deposition is a facile strategy to prepare functional materials but suffers from limitation in thin films and uncontrollable interface engineering. Here we report a universal electrosynthesis of metal hydroxides/oxides on varied substrates via reduction of oxyacid anions. On graphitic substrates, we find that the insertion of nitrate ion in graphene layers significantly enhances the electrodeposit–support interface, resulting in high mass loading and super hydrophilic/aerophobic properties. For the electrocatalytic oxygen evolution reaction, the nanocrystalline cerium dioxide and amorphous nickel hydroxide co-electrodeposited on graphite exhibits low overpotential (177?mV@10?mA?cm?2) and sustains long-term durability (over 300?h) at a large current density of 1000?mA?cm?2. In situ Raman and operando X-ray diffraction unravel that the integration of cerium promotes the formation of electrocatalytically active gamma-phase nickel oxyhydroxide with exposed (003) facets. Therefore, combining anion intercalation with cathodic electrodeposition allows building robust electrodes with high electrochemical performance.
机译:电化学沉积是制备功能材料的简便策略,但受到薄膜的限制和不可控制的界面工程。在这里,我们报告了通过还原含氧酸阴离子在各种基质上普遍进行金属氢氧化物/氧化物的电合成。在石墨基材上,我们发现硝酸根离子在石墨烯层中的插入显着增强了电沉积-载体界面,从而导致了高质量负载和超强的亲水性/疏水性。对于电催化的析氧反应,在石墨上共沉积的纳米二氧化铈和无定形氢氧化镍表现出较低的过电势(177?mV @ 10?mA?cm?2),并在30℃时保持长期耐久性(超过300?h)。 1000?mA?cm?2的大电流密度。原位拉曼光谱和操作X射线衍射表明,铈的整合促进了具有(003)刻面的电催化活性γ-相羟基氧化镍的形成。因此,将阴离子嵌入与阴极电沉积相结合可以构建具有高电化学性能的坚固电极。

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