4.8 Article

Spherical nickel doped cobalt phosphide as an anode catalyst for oxygen evolution reaction in alkaline media: From catalysis to system

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APPLIED CATALYSIS B-ENVIRONMENTAL
卷 327, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.apcatb.2023.122444

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Anion exchange membrane water electrolysis; Oxygen evolution reaction; Anode catalyst; Nickel doped cobalt phosphide

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This study reports the synthesis and characterization of Ni-doped cobalt phosphide catalyst for the anode in anion exchange membrane water electrolysis (AEMWE). The Ni-doping was found to enhance the energy density and charge transfer rate, as well as reduce the energy barrier for OOH* formation, leading to improved electrocatalytic activity. The performance of the catalyst in a membrane-electrode-assembly configuration was evaluated.
Anion exchange membrane water electrolysis (AEMWE) uses a zero-gap membrane-electrode-assembly (MEA) consisting of a polymer electrolyte membrane and non-precious metal-based catalysts. However, anode catalysts for the oxygen evolution reaction (OER), which is the rate-determining-step in WE, need to be intensively developed to achieve superior electrocatalytic activity and stability. Herein, we report the synthesis and characterization (experimental and simulation) of spherical Ni-doped (5-15 at%) cobalt phosphide (Ni-CoP) as the anode catalyst for the OER. Specifically, the DFT calculation exhibited that the addition of Ni in CoP might increase the energy density in the Fermi level of pristine CoP, enhance the charge transfer rate during the OER, and reduce the energy barrier for the formation of OOH* , thereby boosting the OER activity. The prepared Nidoped CoP catalyst was directly loaded onto a foam-type Ni-based gas diffusion layer for effective application in AEMWE. It was found that the electrocatalytic activity of the AEMWE depends on the porosity of the NFs as catalyst substrates. The unit cell containing the membrane-electrode-assembly fabricated with NCP-10 delivered a high current density of 1.12 A cm-2 at 1.8 V and a low reduction rate of 0.64 mA cm-2 h-1 for 250 h.

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