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Core-shell Au-Pd nanoparticles as cathode catalysts for microbial fuel cell applications

机译:核-壳型Au-Pd纳米颗粒作为微生物燃料电池应用的阴极催化剂

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摘要

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.
机译:具有核-壳结构的双金属纳米粒子通常由于核和壳区域之间产生的晶格应变而显示出增强的催化性能。在这项研究中,我们展示了具有Au核和Pd薄壳的双金属Au-Pd纳米颗粒在微生物燃料电池中作为阴极催化剂的应用,这代表着一种有前途的废水处理技术,同时可直接产生电能。具体而言,与中空结构的Pt纳米颗粒(作为电催化的基准)相比,双金属核壳Au-Pd纳米颗粒由于具有强的电子相互作用和抗氧化剂,在中性条件下对氧还原反应具有优异的活性和稳定性。 Au核和Pd壳域之间的晶格应变效应。在以核壳型Au-Pd作为阴极催化剂的废水上运行的无膜单室微生物燃料电池中,产生的最大功率密度约为。 16.0 W m −3 并在150天内保持稳定,这清楚地说明了核壳纳米结构在微生物燃料电池应用中的潜力。

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