在氯化银的存在下,通过电替换反应在镍丝电极上沉积铂纳米颗粒

IF 2.6 4区 化学 Q3 ELECTROCHEMISTRY
Takuma Naito, Akeru Ohama, Syed Shaheen Shah, Zhiwei Cai, Gang Chang, Yunbin He, Munetaka Oyama
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引用次数: 0

摘要

在含有K2PtCl4和AgNO3的水溶液中形成AgCl的悬浮固体。将镍丝浸泡在含有1.0 mM K2PtCl4和1.0 mM AgNO3的水溶液中,浸泡10 min后发现镍丝上沉积了铂纳米粒子(PtNPs),通过观察乙醇氧化的电催化反应以及FE-SEM图像和EDS分析证实了这一点。虽然将镍丝浸泡在仅含K2PtCl4的水溶液中通常不利于PtNPs的沉积,但研究表明,PtCl42−(或其他含有Pt2+的化学物质)与AgCl(和Ag+)共存,促进了与Ni的电取代反应,从而沉积PtNPs。乙醇氧化的电催化反应随制备水溶液[K2PtCl4]和[AgNO3]的不同而发生显著变化;在某些条件下,AgNPs主要沉积。与其他方法制备的PtNPs修饰的Ni (PtNPs/Ni)丝电极相比,所制备的PtNPs/Ni丝电极记录的电催化电流增加了50 mAcm−2以上。图形抽象
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Deposition of platinum nanoparticles on nickel wire electrodes via galvanic replacement reactions enabled by the presence of silver chloride

Suspended solids of AgCl are formed in aqueous solutions containing both K2PtCl4 and AgNO3. When Ni wire is immersed in an aqueous solution containing 1.0 mM K2PtCl4 and 1.0 mM AgNO3, it was found that platinum nanoparticles (PtNPs) were deposited on Ni wire after the immersion of 10 min. This was confirmed by observing the electrocatalytic responses for ethanol oxidation as well as the FE-SEM images with EDS analysis. While the deposition of PtNPs is generally unfavorable on the surface of Ni wire by immersing it in an aqueous solution containing only K2PtCl4, it was clarified that the coexistence of PtCl42− (or other chemical species that contain Pt2+) with AgCl (and Ag+) promoted the galvanic replacement reactions with Ni to deposit PtNPs. The electrocatalytic responses for ethanol oxidation significantly changed depending on [K2PtCl4] and [AgNO3] in aqueous solutions for the preparation; AgNPs were dominantly deposited in some conditions. Compared with PtNPs modified Ni (PtNPs/Ni) wire electrodes prepared using other methods, the electrocatalytic current recorded with the present PtNPs/Ni wire electrodes were increased over 50 mAcm−2.

Graphical abstract

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来源期刊
CiteScore
4.80
自引率
4.00%
发文量
227
审稿时长
4.1 months
期刊介绍: The Journal of Solid State Electrochemistry is devoted to all aspects of solid-state chemistry and solid-state physics in electrochemistry. The Journal of Solid State Electrochemistry publishes papers on all aspects of electrochemistry of solid compounds, including experimental and theoretical, basic and applied work. It equally publishes papers on the thermodynamics and kinetics of electrochemical reactions if at least one actively participating phase is solid. Also of interest are articles on the transport of ions and electrons in solids whenever these processes are relevant to electrochemical reactions and on the use of solid-state electrochemical reactions in the analysis of solids and their surfaces. The journal covers solid-state electrochemistry and focusses on the following fields: mechanisms of solid-state electrochemical reactions, semiconductor electrochemistry, electrochemical batteries, accumulators and fuel cells, electrochemical mineral leaching, galvanic metal plating, electrochemical potential memory devices, solid-state electrochemical sensors, ion and electron transport in solid materials and polymers, electrocatalysis, photoelectrochemistry, corrosion of solid materials, solid-state electroanalysis, electrochemical machining of materials, electrochromism and electrochromic devices, new electrochemical solid-state synthesis. The Journal of Solid State Electrochemistry makes the professional in research and industry aware of this swift progress and its importance for future developments and success in the above-mentioned fields.
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