Abstract

Carbon material containing nickel, nitrogen and sulfur (Ni-NSC) has been synthesized using metal-organic frameworks (MOFs) as precursor by annealing treatment with a size from 200 to 300 nm. Pd nanoparticles supported on the Ni-NSC (Pd/Ni-NSC) are used as electrocatalysts for ethanol oxidation in alkaline media. Due to the synergistic effect between Pd and Ni, S, N, free OH radicals can form on the surface of Ni, N and S atoms at lower potentials, which react with CH3CO intermediate species on the Pd surface to produce CH3COO− and release the active sites. On the other hand, the stronger binding force between Pd and co-doped N and S is responsible for enhancing dispersion and preventing agglomeration of the Pd nanoparticles. The Pd(20 wt%)/Ni-NSC shows better electrochemical performance of ethanol oxidation than the traditional commercial Pd(20 wt%)/C catalyst. Onset potential on the Pd(20 wt%)/Ni-NSC electrode is 36 mV more negative compared with that on the commercial Pd(20 wt%)/C electrode. The Pd(20 wt%)/Ni-NSC in this paper demonstrates to have excellent electrocatalytic properties and is considered as a promising catalyst in alkaline direct ethanol fuel cells.

Highlights

  • Fuel cells are widely recognized as very attractive devices to obtain directly electric energy through an electrochemical reaction between anode and cathode[1]

  • Porous carbon materials synthesized by directly annealing coordination compounds especially metal-organic frameworks (MOFs) possess ultrahigh surface area and periodic network of highly ordered three-dimensional framework structure, which are highly desirable as stable supports to load precious metals[22,23,24,25]

  • Through carbonization and doping steps, the Pd nanoparticles supported on the Ni-NSC (Pd/Ni-NSC) can be successfully obtained

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Summary

Results and Discussion

Pd acts as main catalyst for catalysing the dehydrogenation of ethanol during the oxidation reaction and free OH radicals (OHads) can form on the N or S atoms surface at lower potentials These oxygen containing species react with (CH3CO)ads intermediate species on the Pd surface to produce CH3COO− and release the active sites.

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