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室温下简便合成用于氧还原反应的高活性且稳定的单晶铂多脚架催化剂

Facile Room-Temperature Synthesis of a Highly Active and Robust Single-Crystal Pt Multipod Catalyst for Oxygen Reduction Reaction.

作者信息

Abdelhafiz Ali, Zhao Bote, Xiao Zhuojie, Zeng Jianhuang, Deng Xiang, Lang Leiming, Ding Yong, Song Huiyu, Liu Meilin

机构信息

School of Materials Science and Engineering, Georgia Institute of Technology, 771 Ferst Drive, Atlanta, Georgia 30332-0245, United States.

Guangdong Key Lab for Fuel Cell Technology, School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou 510641, China.

出版信息

ACS Appl Mater Interfaces. 2020 Nov 4;12(44):49510-49518. doi: 10.1021/acsami.0c06652. Epub 2020 Oct 23.

Abstract

Economical production of highly active and robust Pt catalysts on a large scale is vital to the broad commercialization of polymer electrolyte membrane fuel cells. Here, we report a low-cost, one-pot process for large-scale synthesis of single-crystal Pt multipods with abundant high-index facets, in an aqueous solution without any template or surfactant. A composite consisting of the Pt multipods (40 wt %) and carbon displays a specific activity of 0.242 mA/cm and a mass activity of 0.109 A/mg at 0.9 V (versus a reversible hydrogen electrode) for oxygen reduction reaction, corresponding to ∼124% and ∼100% enhancement compared with those of the state-of-the-art commercial Pt/C catalyst (0.108 mA/cm and 0.054 A/mg). The single-crystal Pt multipods also show excellent stability when tested for 4500 cycles in a potential range of 0.6-1.1 V and another 2000 cycles in 0-1.2 V. More importantly, the superior performance of the Pt multipods/C catalyst is also demonstrated in a membrane electrode assembly (MEA), achieving a power density of 774 mW/cm (1.29 A/cm) at 0.6 V and a peak power density of ∼1 W/cm, representing 34% and 20% enhancement compared with those of a MEA based on the state-of-the-art commercial Pt/C catalyst (576 and 834 mW/cm).

摘要

大规模经济地生产高活性和高稳定性的铂催化剂对于聚合物电解质膜燃料电池的广泛商业化至关重要。在此,我们报道了一种低成本的一锅法,用于在无任何模板或表面活性剂的水溶液中大规模合成具有丰富高指数晶面的单晶铂多枝结构。由铂多枝结构(40重量%)和碳组成的复合材料在0.9 V(相对于可逆氢电极)下对氧还原反应的比活性为0.242 mA/cm,质量活性为0.109 A/mg,与目前最先进的商业铂碳催化剂(0.108 mA/cm和0.054 A/mg)相比,分别提高了约124%和100%。单晶铂多枝结构在0.6 - 1.1 V的电位范围内测试4500次循环以及在0 - 1.2 V测试另外2000次循环时也显示出优异的稳定性。更重要的是,铂多枝结构/碳催化剂的优异性能在膜电极组件(MEA)中也得到了证明,在0.6 V时实现了774 mW/cm²(1.29 A/cm²)的功率密度和约1 W/cm²的峰值功率密度,与基于目前最先进的商业铂碳催化剂的MEA(576和834 mW/cm²)相比,分别提高了34%和20%。

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