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This study demonstrates the use of bimetallic Au-Pd nanoparticles as cathode catalysts in microbial fuel cells, showing superior activity and stability for oxygen reduction reaction. The core-shell structure of the nanoparticles creates a lattice strain that enhances their catalytic properties. The maximum power density generated is approximately 16.0 W m⁻³, remaining stable over 150 days.

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What they did

System
MFC

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Abstract

Abstract Bimetallic nanoparticles with core-shell structures usually display enhanced catalytic properties due to the lattice strain created between the core and shell regions. In this study, we demonstrate the application of bimetallic Au-Pd nanoparticles with an Au core and a thin Pd shell as cathode catalysts in microbial fuel cells, which represent a promising technology for wastewater treatment, while directly generating electrical energy. In specific, in comparison with the hollow structured Pt nanoparticles, a benchmark for the electrocatalysis, the bimetallic core-shell Au-Pd nanoparticles are found to have superior activity and stability for oxygen reduction reaction in a neutral condition due to the strong electronic interaction and lattice strain effect between the Au core and the Pd shell domains. The maximum power density generated in a membraneless single-chamber microbial fuel cell running on wastewater with core-shell Au-Pd as cathode catalysts is ca. 16.0 W m −3 and remains stable over 150 days, clearly illustrating the potential of core-shell nanostructures in the applications of microbial fuel cells.

Key findings

  • Bimetallic Au-Pd nanoparticles have superior activity and stability for oxygen reduction reaction
  • The core-shell structure creates a lattice strain that enhances catalytic properties
  • Maximum power density generated is approximately 16.0 W m⁻³

Keywords

Bimetallic stripMicrobial fuel cellElectrocatalystNanoparticleCatalysisCathode

Identifiers

Journal
Scientific Reports
Year
2016