首页> 美国卫生研究院文献>ACS Omega >Facile Synthesis of Quaternary Structurally OrderedL12-Pt(Fe Co Ni)3 Nanoparticles withLow Content of Platinum as Efficient Oxygen Reduction Reaction Electrocatalysts
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Facile Synthesis of Quaternary Structurally OrderedL12-Pt(Fe Co Ni)3 Nanoparticles withLow Content of Platinum as Efficient Oxygen Reduction Reaction Electrocatalysts

机译:四元结构序的简便合成L12-Pt(FeCoNi)3纳米粒子具有低含量的铂作为高效氧还原反应电催化剂

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摘要

Synthesis of electrocatalysts for oxygen reduction reaction (ORR) with not only prominent electrocatalytic performance but also a low amount of Pt is the urgent challenge in the popularization of fuel cells. In this work, through a facile synthetic strategy of spray dehydration on a solid surface and annealing process, we demonstrate the first manufacture of quaternary structurally ordered PtM3 (M = transition metal) intermetallic nanoparticles (NPs), Pt(Fe, Co, Ni)3, in order to lower the content of Pt. The atomic contents of Pt, Fe, Co, and Ni are equal and the chemical structure of Pt(Fe, Co, Ni)3 is a cubic L12-ordered structure. L12-Pt(Fe, Co, Ni)3/C electrocatalysts exhibit enhanced electrocatalytic performance toward ORR with mass activity (MA) 6.6 times higher than the commercial Pt/C and a minimal loss of 17% in MA and 1.5% loss in specific activity (SA) after 10 000 potential cycles at 0.9 V. Furthermore, the stability behavior is confirmed to be attributed to the coaction of particle sizes and the ordering effect. Compared with traditional Pt-based electrocatalystsin the stoichiometric forms of Pt3M and PtM, L12-Pt(Fe, Co, Ni)3 intermetallic NPs exhibit excellent performanceand higher cost effectiveness. Moreover, this work also proposes afacile and effective synthetic strategy for manufacturing multicomponentPt-based electrocatalysts for ORR.
机译:不仅具有突出的电催化性能而且Pt含量低的氧还原反应(ORR)电催化剂的合成是燃料电池普及的迫切挑战。在这项工作中,通过在固态表面上进行喷雾脱水的简便合成策略和退火工艺,我们证明了第一批季铵盐结构化的PtM3(M =过渡金属)金属间纳米颗粒(NPs),Pt(Fe,Co,Ni)的制造3,为了降低Pt的含量。 Pt,Fe,Co和Ni的原子含量相等,并且Pt(Fe,Co,Ni)3的化学结构为立方L12级结构。 L12-Pt(Fe,Co,Ni)3 / C电催化剂对ORR表现出增强的电催化性能,其质量活度(MA)比市售Pt / C高6.6倍,MA的最小损失为17%,特异度的损失为1.5%在0.9 V电压下经过10 000个电势循环后,其活性(SA)。此外,已证实稳定性行为归因于粒径的协同作用和有序作用。与传统的Pt基电催化剂相比以Pt3M和PtM的化学计量形式,L12-Pt(Fe,Co,Ni)3金属间NPs表现出优异的性能以及更高的成本效益。而且,这项工作还提出了制造多组分的简便有效的合成策略铂基ORR的电催化剂。

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