4.8 Article

FeCoP2 Nanoparticles Embedded in N and P Co-doped Hierarchically Porous Carbon for Efficient Electrocatalytic Water Splitting

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 13, 期 7, 页码 8832-8843

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.0c22336

关键词

bimetallic phosphide; N and P co-doped porous carbon; hydrogen evolution reaction; oxygen evolution reaction; water

资金

  1. National Science Foundation of China [21875051, 21805059, 21975058]
  2. Sino-German Center for Research Promotion [GZ1288]

向作者/读者索取更多资源

The FeCoP2@NPPC material synthesized using sustainable biomass-derived precursors exhibits good catalytic activities in hydrogen and oxygen evolution reactions. The synergistic effect between Fe and Co atoms in FeCoP2, as well as the porous carbon matrix and N- and P-containing functionalities, contribute to enhanced electrocatalytic performance for water splitting.
The design and synthesis of low-cost and efficient bifunctional electrocatalysts for water splitting are critical and challenging. Hereby, a bimetallic phosphide embedded in a N and P co-doped porous carbon (FeCoP2@NPPC) material was synthesized by using sustainable biomass-derived N- and P-containing carbohydrates and non-noble metal salts as precursors. The obtained material exhibits good catalytic activities in hydrogen evolution reaction (HER), oxygen evolution reaction (OER), and overall water splitting. The bimetallic alloy phosphide (FeCoP2) is the active site for electrocatalysis. Theoretical calculation indicates that the sub-layer Fe atoms and top-layer Co atoms in FeCoP2 exhibit a synergistic effect for enhanced electrocatalytic performance. The carbon matrix around the FeCoP2 can prevent the corrosion during the catalytic reactions. The hierarchically porous structure of the FeCoP2@NPPC material can promote the transfer of electrons and electrolyte, and increase the contact area of the active sites and electrolytes. N- and P-containing functionalities improve the wetting and conductivity properties of the porous carbon. Due to the synergistic effects, FeCoP2@NPPC requires a low overpotential of 114 and 150 mV at the current density of 10 mA cm(-2) for HER in 0.5 M H2SO4 and 1.0 M KOH, and an overpotential of 236 mV for OER in 1.0 M KOH solution, which are much lower than those of FeP@NPPC and CoP@NPPC. Based on the density functional theory calculation, FeCoP2 yields the smallest Gibbs free energy change of rate-determining step among the samples, which leads to better electrochemical performances. In addition, when FeCoP2@NPPC was used as a bifunctional catalyst in water splitting, the electrolyzer needed a low voltage of 1.60 V to deliver the current density of 10 mA cm(-2). Furthermore, this work provides a strategy for preparing sustainable, stable, and highly active electrocatalysts for water splitting.

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