4.8 Article

Sequential Electrodeposition of Bifunctional Catalytically Active Structures in MoO3/Ni-NiO Composite Electrocatalysts for Selective Hydrogen and Oxygen Evolution

Journal

ADVANCED MATERIALS
Volume 32, Issue 39, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.202003414

Keywords

electrocatalysts; hydrogen evolution reaction; heterointerfaces; oxygen evolution reaction; transition metal oxides; water-splitting

Funding

  1. Young Elite Scientists Sponsorship Program by CAST [2018QNRC001]
  2. National Natural Science Foundation of China [51972224, 51701139]
  3. National Natural Science Foundation of Guangdong Province [U1601216]
  4. China Postdoctoral Science Foundation [2019M661014]

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Exploring earth-abundant and highly efficient electrocatalysts is critical for further development of water electrolyzer systems. Integrating bifunctional catalytically active sites into one multi-component might greatly improve the overall water-splitting performance. In this work, amorphous NiO nanosheets coupled with ultrafine Ni and MoO(3)nanoparticles (MoO3/Ni-NiO), which contains two heterostructures (i.e., Ni-NiO and MoO3-NiO), is fabricated via a novel sequential electrodeposition strategy. The as-synthesized MoO3/Ni-NiO composite exhibits superior electrocatalytic properties, affording low overpotentials of 62 mV at 10 mA cm(-2)and 347 mV at 100 mA cm(-2)for catalyzing the hydrogen and the oxygen evolution reaction (HER/OER), respectively. Moreover, the MoO3/Ni-NiO hybrid enables the overall alkaline water-splitting at a low cell voltage of 1.55 V to achieve 10 mA cm(-2)with outstanding catalytic durability, significantly outperforming the noble-metal catalysts and many materials previously reported. Experimental and theoretical investigations collectively demonstrate the generated Ni-NiO and MoO3-NiO heterostructures significantly reduce the energetic barrier and act as catalytically active centers for selective HER and OER, synergistically accelerating the overall water-splitting process. This work helps to fundamentally understand the heterostructure-dependent mechanism, providing guidance for the rational design and oriented construction of hybrid nanomaterials for diverse catalytic processes.

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