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首页> 外文期刊>Journal of Catalysis >Peptide templated Au@Pd core-shell structures as efficient bi-functional electrocatalysts for both oxygen reduction and hydrogen evolution reactions
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Peptide templated Au@Pd core-shell structures as efficient bi-functional electrocatalysts for both oxygen reduction and hydrogen evolution reactions

机译:肽模板化Au @ Pd核心 - 壳结构作为高效双功能电催化剂,用于氧气还原和氢气进化反应

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摘要

Bimetallic core-shell nanostructures have been gaining considerable research attentions recently, mainly thanks to their versatile applications in many fields, including catalysis, electrocatalysis, electronic, sensing and so on. Herein, we demonstrate a peptide templated Au@Pd core-shell structure for both oxygen reduction reaction (ORR) and hydrogen evolution reaction (HER). By employing peptide sequence FlgA(3) as surface capping agent, core-shell structure with Pd nanoparticles coated on the surface of Au nanoparticles were prepared. The Au@Pd core-shell structures demonstrated effective electrocatalytic activities toward both ORR and HER, whereas the catalytic activity was optimized by tuning the Pd-to-Au ratio. Among a series of samples tested, we discovered that the Au@Pd-1.0 sample exhibited the best ORR activity, superior to that of Pt/C and Pd/C, while its HER activity was also among the finest, close to that of Pt/C and Pd/C. The Au@Pd-1.0 sample also exhibited remarkable stability beyond Pt/C and Pd/C in both ORR and HER. Such intriguing electrocatalytic performances are attributed to the core-shell structure induced lattice strain. The results offer reliable pathway for designing peptide templated core-shell bimetallic nanostructures as dual or multiple functional electrocatalysts with excellent electrocatalytic activities and longevity. (C) 2018 Elsevier Inc. All rights reserved.
机译:最近,双金属核心壳纳米结构一直越来越大,主要是由于它们在许多领域中的多功能应用,包括催化,电殖,电子,传感等。在此,我们证明了用于氧还原反应(ORR)和氢进化反应(她)的肽模板化Au @ Pd核壳结构。通过使用肽序列FLGA(3)作为表面覆盖剂,制备涂覆在Au纳米颗粒表面上的PD纳米颗粒的核 - 壳结构。 Au @ Pd核心壳结构表明了朝向ORR和她的有效电催化活性,而通过调节PD-to-Au比率优化催化活性。在测试的一系列样本中,我们发现Au@pd-1.0样本表现出最佳的ORR活性,优于Pt / c和Pd / c,而她的活动也是最好的,靠近Pt的活动/ c和pd / c。 Au@pd-1.0样品还在orr和她的PT / C和PD / C中表现出显着的稳定性。这种有趣的电催化性能归因于核心壳结构诱导的晶格菌株。结果提供可靠的途径,用于设计肽模板核 - 壳体双金属纳米结构,作为双或多个功能性电催化剂,具有出色的电催化活性和寿命。 (c)2018年Elsevier Inc.保留所有权利。

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