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首页> 外文期刊>Electrochimica Acta >Simple fabrication of core-shell AuPt@Pt nanocrystals supported on reduced graphene oxide for ethylene glycol oxidation and hydrogen evolution reactions
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Simple fabrication of core-shell AuPt@Pt nanocrystals supported on reduced graphene oxide for ethylene glycol oxidation and hydrogen evolution reactions

机译:还原氧化石墨烯负载的核-壳AuPt @ Pt纳米晶体的简单制备,可用于乙二醇氧化和析氢反应

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摘要

Herein, we reported the direct synthesis of core-shell AuPt@Pt nanocrystals supported on reduced graphene oxide (AuPt@Pt NCs/rGO) in aqueous media, with poly(1-vinyl-3-ethylimidazolium bromide) (poly(ViEtlmBr)) as a structure-directing agent, without any specific additive (e.g., seed, organic solvent or template). The as-synthesized AuPt@Pt NCs/rGO exhibited improved electrocatalytic performances towards ethylene glycol oxidation reaction (EGOR) in contrast with commercial Pt/C (20%) catalyst in acidic and alkaline electrolytes. Meanwhile, the catalyst displayed enhanced catalytic activity for hydrogen evolution reaction (HER) with the positive onset potential (-25 mV) and a small Tafel slope (33 mV decade(-1)) relative to Pt/C catalyst (-18 mV, 31 mV decade(-1)) in 0.5 M H2SO4, along with the positive onset potential (-43 mV) and a small Tafel slope (73 mV decade(-1)) as compared with Pt/C catalyst (-42 mV, 85 mV decade(-1)) in 0.5 M KOH. (C) 2016 Elsevier Ltd. All rights reserved.
机译:在这里,我们报道了在水性介质中,用聚(1-乙烯基-3-乙基咪唑鎓溴化物)(poly(ViEtlmBr))直接负载在还原的氧化石墨烯上的核-壳AuPt @ Pt纳米晶体的合成方法作为结构导向剂,无需任何特定的添加剂(例如,种子,有机溶剂或模板)。合成的AuPt @ Pt NCs / rGO与酸性和碱性电解液中的商用Pt / C(20%)催化剂相比,对乙二醇氧化反应(EGOR)表现出改进的电催化性能。同时,相对于Pt / C催化剂(-18 mV),该催化剂显示出更高的催化活性,用于放氢反应(HER),具有正的起始电势(-25 mV)和小的Tafel斜率(33 mV October(-1))。与Pt / C催化剂(-42 mV)相比,在0.5 M H2SO4中的31 mV十进位(-1))以及正的起始电势(-43 mV)和小的Tafel斜率(73 mV十进位(-1))。 85 mV十进位(-1))在0.5 M KOH中。 (C)2016 Elsevier Ltd.保留所有权利。

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