首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Single Nanoparticle Activities in Ensemble: A Study on Pd Cluster Nanoportals for Electrochemical Oxygen Evolution Reaction
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Single Nanoparticle Activities in Ensemble: A Study on Pd Cluster Nanoportals for Electrochemical Oxygen Evolution Reaction

机译:集合体中的单一纳米粒子活性:电化学氧气进化反应PD簇纳米物质的研究

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摘要

Comprehensive understanding of the electrochemical activity of single nanoparticles (NPs) is in critical need for opening new avenues in the broad field of electrochemistry. Published reports on single-NP electrocatalysts typically include complicated and difficult methods of synthesis and characterization; moreover, these methods usually fail to provide a reliable way to measure the activities of individual NPs within larger ensembles of particles, i.e., in real-life nanocatalyst systems. In the present work, we synthesized from the gas phase Pd NPs that act as nanoportals for electron transfer within surface-oxidized Mg thin films. The physical synthesis method provided excellent control over the deposition density and, hence, enabled the design of a system where each individual open nanoportal forms an independent active single-NP electrode (SNPE). Being uncoupled from one another, these SNPEs contribute separately toward the total electrocatalytic activity while simultaneously providing a measure of their average, individual activities. We were thus able to fabricate a stable, steady-state electrode for the electrochemical oxygen evolution reaction (OER) and to study the activity and stability of the SNPEs over a period of 20 days; the former depended on the size of the NPs, while the latter depended on the SNPEs' resistance to aerial oxidation. The remarkable stability of the ensemble catalysts under OER conditions proves that this concept can be used for further studies on the activities of different single NPs in numerous real-life systems.
机译:综合了解单纳米颗粒(NPS)的电化学活性,是在电化学领域开设新途径的关键需求。关于单NP电催化剂的已发表的报告通常包括复杂和困难的合成和表征方法;此外,这些方法通常不能提供可靠的方法来测量在更大的颗粒的颗粒的较大集合中测量单个NP的活动,即在现实纳米催化剂系统中。在本作工作中,我们从气相PD NPS合成,该GD NPS充当纳米滤膜,用于表面氧化的Mg薄膜内的电子转移。物理合成方法提供对沉积密度的优异控制,因此,使得每个单独的开放纳米口形成独立的活性单线电极(SNPE)的系统的设计。这些SnPes彼此脱模,朝向总电催化活动分别贡献,同时提供其平均值的衡量标准。因此,我们能够制造用于电化学氧气进化反应(oer)的稳定,稳态电极,并在20天内研究SNPES的活性和稳定性;前者取决于NPS的大小,而后者依赖于SNPES对空中氧化的抵抗力。在OER条件下,集合催化剂的显着稳定性证明了该概念可用于进一步研究许多现实系统中不同单个NP的活动。

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