Suppr超能文献

在室温离子液体中电沉积铂纳米粒子。

Electrodeposition of platinum nanoparticles in a room-temperature ionic liquid.

机构信息

Department of Electronic Chemistry, Interdisciplinary Graduate School of Science and Engineering, Tokyo Institute of Technology, Nagatsuta 4259-G1-5, Yokohama 226-8502, Japan.

出版信息

Langmuir. 2011 Dec 6;27(23):14662-8. doi: 10.1021/la202992m. Epub 2011 Nov 8.

Abstract

The electrochemistry of the PtCl(6)-PtCl(4)-Pt redox system on a glassy carbon (GC) electrode in a room-temperature ionic liquid (RTIL) [i.e., N,N-diethyl-N-methyl-N-(2-methoxyethyl)ammonium tetrafluoroborate (DEMEBF(4))] has been examined. The two-step four-electron reduction of PtCl(6) to Pt, i.e., reduction of PtCl(6) to PtCl(4) and further reduction of PtCl(4) to Pt, occurs separately in this RTIL in contrast to the one-step four-electron reduction of PtCl(6) to Pt in aqueous media. The cathodic and anodic peaks corresponding to the PtCl(6)/PtCl(4) redox couple were observed at ca. -1.1 and 0.6 V vs a Pt wire quasi-reference electrode, respectively, while those observed at -2.8 and -0.5 V were found to correspond to the PtCl(4)/Pt redox couple. The disproportionation reaction of the two-electron reduction product of PtCl(6) (i.e., PtCl(4)) to PtCl(6) and Pt metal was also found to occur significantly. The electrodeposition of Pt nanoparticles could be carried out on a GC electrode in DEMEBF(4) containing PtCl(6) by holding the potential at -3.5 or -2.0 V. At -3.5 V, the four-electron reduction of PtCl(6) to Pt can take place, while at -2.0 V the two-electron reduction of PtCl(6) to PtCl(4) occurs. The results obtained demonstrate that the electrodeposition of Pt at -3.5 V may occur via a series of reductions of PtCl(6) to PtCl(4) and further PtCl(4) to Pt and at -2.0 V via a disproportionation reaction of PtCl(4) to PtCl(6) and Pt. Furthermore, the deposition potential of Pt nanoparticles was found to largely influence their size and morphology as well as the relative ratio of Pt(110) and Pt(100) crystalline orientation domains. The sizes of the Pt nanoparticles prepared by holding the electrode potential at -2.0 and -3.5 V are almost the same, in the range of ca. 1-2 nm. These small nanoparticles are "grown" to form bigger particles with different morphologies: In the case of the deposition at -2.0 V, the GC electrode surface is totally, relatively compactly covered with Pt particles of relatively uniform size of ca. 10-50 nm. On the other hand, in the case of the electrodeposition at -3.5 V, small particles of ca. 50-100 nm and the grown-up particles of ca. 100-200 nm cover the GC surface irregularly and coarsely. Interestingly, the Pt nanoparticles prepared by holding the potential at -2.0 and -3.5 V are relatively enriched in Pt(100) and Pt(110) facets, respectively.

摘要

在室温离子液体(即 N,N-二乙基-N-甲基-N-(2-甲氧基乙基)铵四氟硼酸盐(DEMEBF4))中,研究了PtCl6-PtCl4-Pt 氧化还原体系在玻璃碳(GC)电极上的电化学行为。与在水溶液中PtCl6一步四电子还原为 Pt 不同,PtCl6在这种 RTIL 中分步发生四电子还原为 Pt,即PtCl6还原为PtCl4,然后PtCl4进一步还原为 Pt。与 Pt 丝准参比电极相比,分别在约-1.1 和 0.6 V 处观察到对应于PtCl6/PtCl4氧化还原对的阴极和阳极峰,而在-2.8 和-0.5 V 处观察到的峰则对应于PtCl4/Pt 氧化还原对。还发现PtCl6的两电子还原产物(即PtCl4)歧化反应也显著发生。通过将电位保持在-3.5 或-2.0 V,可以在含有PtCl6的 DEMEBF4中在 GC 电极上电沉积 Pt 纳米颗粒。在-3.5 V 时,PtCl6可以发生四电子还原为 Pt,而在-2.0 V 时,PtCl6发生两电子还原为PtCl4。所得结果表明,在-3.5 V 下 Pt 的电沉积可能通过PtCl6还原为PtCl4和进一步还原为 Pt 的一系列还原反应发生,而在-2.0 V 下通过PtCl4歧化反应发生还原为PtCl6和 Pt。此外,Pt 纳米颗粒的沉积电位极大地影响它们的尺寸和形态以及 Pt(110)和 Pt(100)晶面取向域的相对比例。通过将电极电位保持在-2.0 和-3.5 V 来制备的 Pt 纳米颗粒的尺寸几乎相同,约为 1-2 nm。这些小纳米颗粒“生长”成具有不同形态的更大颗粒:在-2.0 V 的沉积情况下,GC 电极表面完全、相对紧密地覆盖有大小约为 10-50 nm 的相对均匀的 Pt 颗粒。另一方面,在-3.5 V 的电沉积情况下,约 50-100 nm 的小颗粒和约 100-200 nm 的生长颗粒不规则地、粗糙地覆盖 GC 表面。有趣的是,通过将电位保持在-2.0 和-3.5 V 制备的 Pt 纳米颗粒分别相对富含 Pt(100)和 Pt(110)晶面。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验