4.7 Article

Free-standing two-dimensional ruthenium-beryllium nanosheets for alkaline hydrogen evolution

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 421, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2021.129741

Keywords

Ruthenium; Nanosheets; Hydrogen evolution; Alloy

Funding

  1. National Natural Science Foundation of China [51602116]
  2. Natural Science Foundation of Anhui Province [1708085QB40]

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In this study, free-standing ruthenium-beryllium (RuBe) nanosheets with amorphous phase state and holey structures were synthesized successfully using a facile approach. The 2D RuBe nanosheets exhibit improved activity compared to pure Ru and comparable properties to commercial Pt for hydrogen evolution reaction in both alkaline and neutral electrolytes. The enhanced adsorption and dissociation of water molecules on Ru-based catalyst with Be modulation are essential for the improved hydrogen production capability under alkaline condition. This work expands the Ru-based catalyst family and may provide new insights for electrocatalyst development.
To design and synthesize materials for alkaline hydrogen evolution is favorable for industrial hydrogen cycle operation. In this study, we present a facile approach to synthesize free-standing ruthenium-beryllium (RuBe) nanosheets, which possess amorphous phase state and associated with holey structures due to the molten method. The two-dimensional RuBe nanosheets exhibit improved activity than pure Ru counterpart and comparable properties to commercial Pt toward hydrogen evolution reaction in both of alkaline and neutral electrolytes. Based on the experiments and density functional theory calculations, it is suggested that the adsorption and dissociation of water molecules on Ru-based catalyst are much enhanced with the assistance of Be modulation, which are essential for the improved hydrogen production capability under alkaline condition. This work broadens the Ru-based catalyst family and may provide new insights for electrocatalyst development.

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