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Ni3+-Induced Formation of Active NiOOH on the Spinel Ni–Co Oxide Surface for Efficient Oxygen Evolution Reaction

机译:Ni3 +诱导在尖晶石Ni-Co氧化物表面上形成活性NiOOH,以进行有效的放氧反应

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摘要

Efficient and earth abundant electrocatalysts for high-performance oxygen evolution reaction (OER) are essential for the development of sustainable energy conversion technologies. Here, a new hierarchical Ni–Co oxide nanostructure, composed of small secondary nanosheets grown on primary nanosheet arrays, is synthesized via a topotactic transformation of Ni–Co layered double hydroxide. The Ni3+-rich surface benefits the formation of NiOOH, which is the main redox site as revealed via in situ X-ray absorption near edge structure and extended X-ray absorption fine structure spectroscopy. The Ni–Co oxide hierarchical nanosheets (NCO–HNSs) deliver a stable current density of 10 mA cm−2 at an overpotential of ≈0.34 V for OER with a Tafel slope of as low as 51 mV dec−1 in alkaline media. The improvement in the OER activity can be ascribed to the synergy of large surface area offered by the 3D hierarchical nanostructure and the facile formation of NiOOH as the main active sites on the surface of NCO–HNSs to decrease the overpotential and facilitate the catalytic reaction.
机译:高效的氧气释放反应(OER)所需的高效和富含地球的电催化剂对于可持续能源转换技术的发展至关重要。在这里,通过对Ni-Co层状双氢氧化物进行定势转变,合成了一个新的分层Ni-Co氧化物纳米结构,该结构由在初级纳米片阵列上生长的小的次级纳米片组成。富含Ni3 +的表面有利于NiOOH的形成,这是通过边缘结构附近的原位X射线吸收和扩展X射线吸收精细结构光谱揭示的主要氧化还原位点。 Ni-Co氧化物分层纳米片(NCO-HNSs)在OER的约0.34 V超电势下,在碱性介质中的Tafel斜率低至51 mV dec-1,可提供10 mA cm-2的稳定电流密度。 OER活性的提高可归因于3D分层纳米结构提供的大表面积协同作用,以及作为NCO-HNSs表面主要活性位点的NiOOH的便捷形成,以减少过电势并促进催化反应。

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