首页> 外文期刊>Journal of Materials Chemistry, A. Materials for energy and sustainability >Self-standing non-noble metal (Ni-Fe) oxide nanotube array anode catalysts with synergistic reactivity for high-performance water oxidation
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Self-standing non-noble metal (Ni-Fe) oxide nanotube array anode catalysts with synergistic reactivity for high-performance water oxidation

机译:具有协同反应活性的自立非贵金属(Ni-Fe)氧化物纳米管阵列阳极催化剂,用于高效水氧化

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摘要

The oxygen evolution reaction (OER) is coupled with a number of important cathodic processes, for instance water splitting for hydrogen production and other energy storage devices based on O-2-H2O chemistries such as metal-air batteries and unitized regenerative fuel cells, but they are limited by the slow kinetics. Attempts to solve this problem have received wide attention recently. However, accessing and stabilizing high-oxidation-state catalytically active species to further improve the high performance for the OER has been considered a huge challenge. Here, we report a Ni-Fe oxide-based nanotube array electrode, novel in design, with strong durability and excellent and synergistically enhanced catalytic performance for the OER. The OER electrode, with a nanotube array nanostructure, shows the remarkable features of a small overpotential of 0.28 V, favourable electrode kinetics and high stability, comparing favorably with the reported performances of the best OER electrocatalysts (IrO2), which is attributed to the formation and stabilization of the favourable OER catalytically active species NiOOH that is produced and reinforced by the introduction of Fe into nanostructured materials. This feasible strategy affords a new strategy for the development of effective and robust OER electrodes.
机译:氧气逸出反应(OER)与许多重要的阴极过程相结合,例如用于制氢的水分解和其他基于O-2-H2O化学性质的储能装置,例如金属空气电池和组合式再生燃料电池,但是它们受到慢速动力学的限制。解决该问题的尝试近来受到广泛关注。然而,进入和稳定高氧化态催化活性物质以进一步提高OER的高性能被认为是巨大的挑战。在这里,我们报告了一种设计新颖,耐用性强,对OER具有出色且协同增强的催化性能的镍-铁氧化物基纳米管阵列电极。具有纳米管阵列纳米结构的OER电极具有0.28 V的小过电位,良好的电极动力学和高稳定性的显着特征,与报告的最佳OER电催化剂(IrO2)的性能相比具有优势,这归因于形成以及通过将铁引入纳米结构材料中而产生和增强的良好的OER催化活性物种NiOOH的稳定性。这种可行的策略为开发有效而坚固的OER电极提供了新的策略。

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