4.7 Article

Synthesis of hollow CoSe2/MoSe2 nanospheres for efficient hydrazineassisted hydrogen evolution

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 404, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2020.126529

Keywords

CoSe2/MoSe2 composites; Hollow nanospheres; Hydrogen evolution reaction; Hydrazine oxidation reaction; Interfacial engineering

Funding

  1. National Key R&D Program of China [2016YFA0204000, 2018YFA0209401, 2018YFE0201701]
  2. National Natural Science Foundation of China [21733003, 21975050]
  3. Science and Technology Commission of Shanghai Municipality [17JC1400100, 19JC1410700]

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This work presents a facile synthesis strategy to prepare hollow CoSe2/MoSe2 nanospheres with abundant active interfaces for hydrazine-assisted hydrogen production. Benefiting from the active interfaces, the hollow nanosphere exhibits excellent performance in terms of low overpotential for HER and HzOR, making it a promising bifunctional electrocatalyst for energy-saving electrolytic hydrogen production.
Hydrazine-assisted hydrogen evolution cell has been regarded as a promising route to replace conventional water splitting because of the lower thermodynamic oxidation potential. Therefore, the design and synthesis of highly efficient bifunctional electrocatalysts for anodic hydrazine oxidation reaction (HzOR) and cathodic hydrogen evolution reaction (HER) are crucial and highly desired. In this work, we report a facile synthesis strategy to prepare hollow CoSe2/MoSe2 nanospheres with abundant active interfaces for hydrazine-assisted hydrogen production. The homogeneous mixing of Co and Mo ions in the metal organic framework precursors ensures the formation of intimately contacted interfaces after selenization, leading to the reinforced concrete CoSe2/ MoSe2 composites. Benefiting from the CoSe2/MoSe2 interfaces, the hollow CoSe2/MoSe2 nanosphere performs a low HER overpotential of 168 mV with an excellent stability over 12 h. Additionally, it also exhibits a low overpotential of 386 mV (vs. RHE) for HzOR and an ultralow cell voltage (1 mA cm(-2)) of 160 mV, which are among the best reported performance of powdered electrocatalysts. The present work develops a promising bifunctional electrocatalyst with active interfaces for energy-saving electrolytic hydrogen production.

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