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镍纳米颗粒与Ni C纳米片的协同耦合用于高效全解水

Synergistic Coupling of Ni Nanoparticles with Ni C Nanosheets for Highly Efficient Overall Water Splitting.

作者信息

Wang Pengyan, Qin Rui, Ji Pengxia, Pu Zonghua, Zhu Jiawei, Lin Can, Zhao Yufeng, Tang Haolin, Li Wenqiang, Mu Shichun

机构信息

State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan, 430070, P. R. China.

Foshan Xianhu Laboratory, Foshan, 528200, P. R. China.

出版信息

Small. 2020 Sep;16(37):e2001642. doi: 10.1002/smll.202001642. Epub 2020 Aug 6.

Abstract

Exploring earth-abundant bifunctional electrocatalysts with high efficiency for water electrolysis is extremely demanding and challenging. Herein, density functional theory (DFT) predictions reveal that coupling Ni with Ni C can not only facilitate the oxygen evolution reaction (OER) kinetics, but also optimize the hydrogen adsorption and water adsorption energies. Experimentally, a facile strategy is designed to in situ fabricate Ni C nanosheets on carbon cloth (CC), and simultaneously couple with Ni nanoparticles, resulting in the formation of an integrated heterostructure catalyst (Ni-Ni C/CC). Benefiting from the superior intrinsic activity as well as the abundant active sites, the Ni-Ni C/CC electrode demonstrates excellent bifunctional electrocatalytic activities toward the OER and hydrogen evolution reaction (HER), which are superior to all the documented Ni C-based electrocatalysts in alkaline electrolytes. Specifically, the Ni-Ni C/CC catalyst exhibits the low overpotentials of only 299 mV at the current density of 20 mA cm for the OER and 98 mV at 10 mA cm for the HER in 1 m KOH. Furthermore, the bifunctional Ni-Ni C/CC catalyst can propel water electrolysis with excellent activity and nearly 100% faradic efficiency. This work highlights an easy approach for designing and constructing advanced nickel carbide-based catalysts with high activity based on the theoretical predictions.

摘要

探索用于水电解的具有高效性的地球丰富双功能电催化剂极具挑战性。在此,密度泛函理论(DFT)预测表明,将镍与碳化镍耦合不仅可以促进析氧反应(OER)动力学,还能优化氢吸附和水吸附能。在实验方面,设计了一种简便策略,原位在碳布(CC)上制备碳化镍纳米片,并同时与镍纳米颗粒耦合,从而形成一种集成异质结构催化剂(Ni-NiC/CC)。受益于优异的本征活性以及丰富的活性位点,Ni-NiC/CC电极对OER和析氢反应(HER)表现出优异的双功能电催化活性,在碱性电解质中优于所有已报道的基于碳化镍的电催化剂。具体而言,在1 M KOH中,Ni-NiC/CC催化剂在20 mA cm²的电流密度下对于OER表现出仅299 mV的低过电位,在10 mA cm²下对于HER表现出98 mV的低过电位。此外,双功能Ni-NiC/CC催化剂能够以优异的活性和近100%的法拉第效率推动水电解。这项工作突出了一种基于理论预测设计和构建具有高活性的先进碳化镍基催化剂的简便方法。

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