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镍-氧化镍异质结:一种用于增强析氧反应的无粘结剂催化剂。

Ni-NiO Heterojunction: A Binder-Free Catalyst for Enhanced Oxygen Evolution Reaction.

作者信息

Farahbakhsh Nastaran, Shahsanaei Majid, Hartwich Patrick, Mohajernia Shiva, Killian Manuela S, Hejazi Sina

机构信息

Chemistry and Structure of novel Materials, Department of Chemistry and Biology, University of Siegen, Paul-Bonatz-Str. 9-11, Siegen 57076, Germany.

Department of Chemical and Materials Engineering, Faculty of Engineering, University of Alberta, Edmonton, Alberta T6G 1H9, Canada.

出版信息

ACS Omega. 2025 Aug 25;10(35):39451-39462. doi: 10.1021/acsomega.4c10355. eCollection 2025 Sep 9.

Abstract

In this study, we applied a two-step electrochemical anodization process to produce highly porous nanostructured nickel suboxides. We then annealed these materials in different environments: air, Ar, and Ar/H. Annealing in a reductive environment (Ar/H) resulted in a Ni-NiO heterojunction with a high defect density, as confirmed by the Mott-Schottky analysis. Our results demonstrate that these defects and active sites significantly enhance the electrocatalytic activity for the oxygen evolution reaction (OER). Utilizing X-ray photoelectron spectroscopy (XPS), field emission scanning electron microscopy (FE-SEM), high-resolution transmission electron microscopy (HR-TEM), and electrochemical analysis, we demonstrate that the heterojunction system containing Ni-NiO, formed through annealing in an Ar/H atmosphere, acts as a highly efficient electrocatalyst for the OER. This catalyst achieves an impressively low overpotential of 293 mV at 10 mA cm, a Tafel slope of 74 mV dec, and exhibits outstanding stability, maintaining performance over 1000 cycles. Notably, our most optimized NiO electrode outperforms the conventional reference RuO electrode by a factor of 1.72. Our findings demonstrate the potential of binder-free Ni-NiO heterojunctions in developing high-performance electrocatalysts for alkaline electrolysis.

摘要

在本研究中,我们采用两步电化学阳极氧化工艺制备了高度多孔的纳米结构氧化镍。然后,我们在不同环境中对这些材料进行退火处理:空气、氩气和氩气/氢气。如莫特-肖特基分析所证实,在还原环境(氩气/氢气)中退火会产生具有高缺陷密度的镍-氧化镍异质结。我们的结果表明,这些缺陷和活性位点显著增强了析氧反应(OER)的电催化活性。利用X射线光电子能谱(XPS)、场发射扫描电子显微镜(FE-SEM)、高分辨率透射电子显微镜(HR-TEM)和电化学分析,我们证明,通过在氩气/氢气气氛中退火形成的含镍-氧化镍的异质结体系可作为OER的高效电催化剂。该催化剂在10 mA cm时实现了低至293 mV的过电位、74 mV dec的塔菲尔斜率,并表现出出色的稳定性,在1000次循环中保持性能。值得注意的是,我们最优化的氧化镍电极的性能比传统的参比RuO电极高出1.72倍。我们的研究结果表明,无粘结剂的镍-氧化镍异质结在开发用于碱性电解的高性能电催化剂方面具有潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e49/12423888/a9f8c307d3a8/ao4c10355_0001.jpg

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