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Graphitic carbon-based core-shell platinum electrocatalysts processed using nickel nanoparticle template for oxygen reduction reaction

机译:使用镍纳米粒子模板进行氧还原反应的石墨基碳基核心壳催化剂

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摘要

Extensive efforts have aimed at securing stable Pt-based electrocatalysts having both the performance-efficiency and long-term durability particularly for proton-exchange membrane fuel cells. Herein, we introduce an unprecedented electrocatalyst architecture based on a core-shell phase-mediated Pt/carbon black (CB) support structure which was enabled by the graphitization process using a Ni nanoparticle template. A similar to 1.03 nm-thick shell layer of graphitic carbon (GC) formed around the surface of similar to 9 nm-scale Ni core-nanoparticles via the dissolution-precipitation process with the annealing step of Ni on CB. The final Pt/GC/Ni/CB catalyst demonstrated noticeably better electrocatalytic performance in oxygen reduction reaction than that of the catalyst without the GC layer. The accelerated durability test with 5,000 cycles confirmed the advantages of the GC shell layer by demonstrating less electrochemical degradations by similar to 4.4 times in electrochemical surface area and similar to 2.5 times in the half-wave potential, compared to those of the reference sample.
机译:广泛的努力旨在确保具有性能效率和长期耐久性的稳定的PT基电催化剂,特别是对于质子交换膜燃料电池。在此,我们基于使用Ni纳米颗粒模板的石墨化方法实现的基于核 - 壳相介导的Pt /炭黑(CB)支持结构引入前所未有的电催化剂架构。类似于通过溶解 - 沉淀方法在类似于9nm级Ni核心纳米颗粒的表面周围形成的1.03nm厚的石墨碳(GC),通过溶解 - 沉淀方法在CB上的退火步骤。最终的Pt / GC / Ni / Cb催化剂在氧还原反应中明显更好地进行了电催化性能,而不是没有GC层的催化剂。通过5,000个循环的加速耐久性试验通过在电化学表面积中的4.4倍类似于4.4次的情况下证明了GC壳层的优点,与参考样品相比,在半波电位中类似于半波电位的2.5倍。

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