Department of Chemistry, State University of New York at Stony Brook, Stony Brook, New York 11794-3400, USA.
ACS Appl Mater Interfaces. 2013 Jun 26;5(12):5518-30. doi: 10.1021/am4007462. Epub 2013 Jun 6.
We report for the first time (a) the synthesis of elemental ruthenium nanowires (Ru NWs), (b) a method for modifying their surfaces with platinum (Pt), and (c) the morphology-dependent methanol oxidation reaction (MOR) performance of high-quality Pt-modified Ru NW electrocatalysts. The synthesis of our elemental Ru NWs has been accomplished utilizing a template-based method under ambient conditions. As-prepared Ru NWs are crystalline and elementally pure, maintain electrochemical properties analogous to elemental Ru, and can be generated with average diameters ranging from 44 to 280 nm. We rationally examine the morphology-dependent performance of the Ru NWs by comparison with commercial Ru nanoparticle (NP)/carbon (C) systems after decorating the surfaces of these structures with Pt. We have demonstrated that the deposition of Pt onto the Ru NWs (PtRu NWs) results in a unique hierarchical structure, wherein the deposited Pt exists as discrete clusters on the surface. By contrast, we find that the Pt-decorated commercial Ru NP/C (PtRu NP/C) results in the formation of an alloy-type NP. The PtRu NPs (0.61 A/mg of Pt) possess nearly 2-fold higher Pt mass activity than analogous PtRu NW electrocatalysts (0.36 A/mg of Pt). On the basis of a long-term durability test, it is apparent that both catalysts undergo significant declines in performance, potentially resulting from aggregation and ripening in the case of PtRu NP/C and the effects of catalyst poisoning in the PtRu NWs. At the conclusion of the test, both catalysts maintain comparable performance, despite a slightly enhanced performance in PtRu NP/C. In addition, the measured mass-normalized MOR activity of the PtRu NWs (0.36 A/mg of Pt) was significantly enhanced as compared with supported elemental Pt (Pt NP/C, 0.09 A/mg of Pt) and alloy-type PtRu (PtRu NP/C, 0.24 A/mg of Pt) NPs, both serving as commercial standards.
(a) 元素钌纳米线 (Ru NWs) 的合成;(b) 用铂 (Pt) 修饰其表面的方法;(c) 高质量 Pt 修饰 Ru NW 电催化剂的形态依赖性甲醇氧化反应 (MOR) 性能。我们的元素 Ru NWs 是通过在常温常压下利用模板法合成的。所制备的 Ru NWs 是结晶的且元素纯的,保持与元素 Ru 类似的电化学性能,并且可以生成平均直径为 44 至 280nm 的 Ru NWs。我们通过与商业 Ru 纳米颗粒 (NP)/碳 (C) 系统进行比较,合理地考察了 Ru NWs 的形态依赖性性能,在这些结构的表面上用 Pt 修饰后。我们已经证明,Pt 在 Ru NWs 上的沉积 (PtRu NWs) 导致独特的分层结构,其中沉积的 Pt 以离散的簇存在于表面上。相比之下,我们发现 Pt 修饰的商业 Ru NP/C (PtRu NP/C) 导致形成合金型 NP。PtRu NPs(0.61A/mgPt) 的 Pt 质量活性比类似的 PtRu NW 电催化剂(0.36A/mgPt)高近 2 倍。基于长期耐久性测试,显然两种催化剂的性能都有明显下降,这可能是由于 PtRu NP/C 中的团聚和成熟以及 PtRu NWs 中的催化剂中毒效应造成的。在测试结束时,尽管 PtRu NP/C 的性能略有提高,但两种催化剂的性能仍保持可比。此外,PtRu NWs 的质量归一化 MOR 活性 (0.36A/mgPt) 明显高于负载型元素 Pt(Pt NP/C,0.09A/mgPt) 和合金型 PtRu(PtRu NP/C,0.24A/mgPt),两者均为商业标准。