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

机译:核 - 壳AU-Pd纳米粒子作为用于微生物燃料电池应用的阴极催化剂

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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颗粒通常由于芯和壳区域之间产生的晶格菌株而显示增强的催化性能。在该研究中,我们证明了双金属Au-Pd纳米颗粒在微生物燃料电池中用Au芯和薄Pd壳作为阴极催化剂的应用,这代表了用于废水处理的有希望的技术,同时直接产生电能。具体而言,与中空结构化Pt纳米颗粒相比,电常放分析的基准,发现双金属芯 - 壳AU-Pd纳米颗粒具有优异的活性和由于强电子互动而在中性条件下的氧还原反应的稳定性。晶格应变效应Au核和PD壳域。在具有Core-Shell Au-Pd的废水上运行的膜单室微生物燃料电池中产生的最大功率密度是阴极催化剂是Ca。 16.0?W m(-3)并保持稳定超过150天,清楚地说明核心 - 壳纳米结构在微生物燃料电池的应用中的潜力。

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