石墨烯负载的镍纳米颗粒增强电催化水氧化性能

Yan Yan , Mengyu Lu , Shifu Zhang, Mei Wang, Tongbu Lu
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引用次数: 0

摘要

在电催化水氧化反应(OER)中,钌和铱等贵金属的替代是一个非常重要的技术问题。然而,尽管最近取得了进展,用于OER的非贵金属的发展仍然受到其高过电位,缓慢的动力学和不充分的稳定性的阻碍。优化非贵重过渡金属纳米材料的电子结构对提高其电催化OER性能起着至关重要的作用。在这项研究中,我们采用一种简单的还原方法将镍纳米颗粒原位负载到石墨炔(GDY)上,并获得了Ni NPs/GDY催化剂。由于GDY独特的化学和物理性质,它与镍纳米粒子的结合产生了强的电子相互作用,有效地调节了Ni NPs/GDY催化剂的电子和几何结构,显著提高了其在OER中的电催化性能。Ni NPs/GDY催化剂在电流密度为10 mA cm−2时的过电位低至294 mV,在1 M KOH下的Tafel斜率小至56.8 mV dec−1,具有优异的电催化动力学性能和约90 h的超长电催化稳定性。与参考催化剂Ni NPs和GDY相比,Ni NPs/GDY催化剂表现出优异的性能。这主要是由于镍纳米颗粒在GDY上负载时产生的电子相互作用,在催化过程中可以暴露更多的催化位点,促进电荷转移,同时防止催化剂聚集。本工作的发现可以为探索更高效的OER电催化剂提供新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Graphdiyne-supported nickel nanoparticles for enhanced electrocatalytic water oxidation performance

Graphdiyne-supported nickel nanoparticles for enhanced electrocatalytic water oxidation performance
The substitution of precious metals, such as ruthenium and iridium, to boost the performance of the electrocatalytic water oxidation reaction (OER) is of paramount importance in energy science and technology. However, despite recent advances, the development of nonprecious metals for the OER is still hindered by their high overpotentials, sluggish kinetics, and inadequate stability. Optimization of the electronic structure of non-precious transition metal nanomaterials plays a crucial role in enhancing their performance in the electrocatalytic OER. In this study, we employed a facile reduction method for the in situ loading of nickel nanoparticles onto graphdiyne (GDY) and obtained the Ni NPs/GDY catalyst. Due to the distinctive chemical and physical properties of GDY, its combination with nickel nanoparticles results in strong electronic interactions, effectively modulating the electronic and geometric structures of the Ni NPs/GDY catalyst and significantly improving its electrocatalytic performance in the OER. The Ni NPs/GDY catalyst exhibited a low overpotential of 294 mV at a current density of 10 mA cm2 and a small Tafel slope of 56.8 mV dec1 in 1 M KOH, along with excellent electrocatalytic kinetic properties and an ultra-long electrocatalytic stability of approximately 90 h. Compared to the reference catalysts Ni NPs and GDY, the Ni NPs/GDY catalyst demonstrated superior performance, which is primarily attributed to the electronic interactions generated upon the loading of nickel nanoparticles to GDY, which can expose more catalytic sites, facilitate charge transfer, and simultaneously prevent catalyst aggregation during the catalytic process. The findings of this work can provide new insights for exploring more efficient electrocatalysts for the OER.
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