Ambient Surfactantless Synthesis, Growth Mechanism, and Size-Dependent Electrocatalytic Behavior of High-Quality, Single Crystalline Palladium Nanowires
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- 作者：Christopher Koenigsmann ; Alexander C. Santulli ; Eli Sutter ; Stanislaus S. Wong
- 刊名：ACS Nano
- 出版年：2011
- 出版时间：September 27, 2011
- 年：2011
- 卷：5
- 期：9
- 页码：7471-7487
- 全文大小：1368K
- 年卷期：0
- ISSN：1936-086X
文摘
In this report, we utilize the U-tube double diffusion device as a reliable, environmentally friendly method for the size-controlled synthesis of high-quality, single crystalline Pd nanowires. The nanowires grown in 200 and 15 nm polycarbonate template pores maintain diameters of 270 ± 45 nm and 45 ± 9 nm, respectively, and could be isolated either as individual nanowires or as ordered free-standing arrays. The growth mechanism of these nanowires has been extensively explored, and we have carried out characterization of the isolated nanowires, free-standing nanowire arrays, and cross sections of the filled template in order to determine that a unique two-step growth process predominates within the template pores. Moreover, as-prepared submicrometer and nanosized wires were studied by comparison with ultrathin 2 nm Pd nanowires in order to elucidate the size-dependent trend in oxygen reduction reaction (ORR) electrocatalysis. Subsequently, the desired platinum monolayer overcoating was reliably deposited onto the surface of the Pd nanowires by Cu underpotential deposition (UPD) followed by galvanic displacement of the Cu adatoms. The specific and platinum mass activity of the core–shell catalysts was found to increase from 0.40 mA/cm2 and 1.01 A/mg to 0.74 mA/cm2 and 1.74 A/mg as the diameter was decreased from the submicrometer size regime to the ultrathin nanometer range.