• Vanrompay, Hans
• Sentosun, Kadir
• Bouckenooge, Pieter
• Cherigui, El Amine Mernissi
• Terryn, Herman
• Bals, Sara
• Ustarroz, Jon

Abstract

Supported nickel nanoparticles are widely used as catalysts for fuel cells and electrosynthesis, as well as for biosensors and supercapacitors. These nanomaterials can be fabricated by multiple methods. However, electrodeposition offers several advantages since it permits the growth of the nanoparticles (NPs) directly on the support of interest and allows obtaining highly electroactive nanostructures [1]. In order to produce highly electroactive nanostructures, the electrochemical processes on the nanoscale need to be understood. In this context, Deep Eutectic Solvents (DESs) have generated great enthusiasm as a new generation of non-aqueous electrolytes. They offer plenty of advantages, such as high stability at higher temperatures and broad electrochemical window compared to aqueous solutions. Furthermore, DESs are easier to prepare, less toxic and much cheaper than room temperature ionic liquids (RTILs) [2].A recent approach, based on using carbon coated TEM grids as electrochemical electrodes, was developed in our group in order to study, at the nano-scale, the electrodeposited structures directly from the supporting substrate [3]. In this work, we used this approach to study the electrodeposition of nickel nanostructures from 1:2 choline chloride – urea DES (1:2 ChCl-U). By combining electrochemical techniques, such us cyclic / linear sweep voltammetry and chronoamperommetry, with ex-situ characterization, like FE-SEM, XPS, STEM, EDX and EELS, the electrochemical processes occurring during nickel deposition were better understood. Special attention was given to the interaction between the solvent and the electrodeposited nickel phase. In the frame of this investigation, a large population of small crystalline nickel nanostructures (< 20-50 nm) was obtained within a wide range of deposition parameters. Interestingly, we have found evidences that support the presence of an interaction between the DES and the growing nickel NPs that could lead to a self-limiting growth mechanism [4]. Indeed, the nanostructures obtained are formed by aggregated nanoclusters of few nanometers in diameter [5]. These results show that metal electrodeposition from DESs can be of great interest to produce nanostructures with electrocatalytic properties in a controllable and efficient way.[1] G-R. Li, H. Xu, X-F. Lu, J-X. Feng, Y-X. Tong, C-Y. Su, Electrochemical synthesis of nanostructured materials for electrochemical energy conversion and storage. Nanoscale, 5 (2013), 4056-4069. [2] E.L. Smith, A.P. Abbott, K.S. Ryder, Deep eutectic solvents (DESs) and their applications. Chemical Reviews, 114, (2014), 11060–82. [3] J. Ustarroz, J.A. Hammons, T. Altantzis, A. Hubin, S. Bals, H. Terryn, A generalized electrochemical aggregative growth mechanism. Journal of the American Chemical Society, 135 (2013), 11550–11561. [4]J.A. Hammons, T. Muselle, J. Ustarroz, M. Tzedaki, M. Raes, A. Hubin, et al., Stability, Assembly, and Particle/Solvent Interactions of Pd Nanoparticles Electrodeposited from a Deep Eutectic Solvent, The Journal of Physical Chemistry C. 117 (2013) 14381–14389. [5]E.A. Mernissi Cherigui, P. Bouckenooge, K. Sentosun, H. Vanrompay, S. Bals, J. Ustarroz, H. Terryn,Electrodeposition of Nickel Nanostructures from Deep Eutectic Solvents, Manuscript in Preparation. (2016).

Topics

• nanoparticle
• Carbon
• nickel
• phase
• x-ray photoelectron spectroscopy
• laser emission spectroscopy
• transmission electron microscopy
• Energy-dispersive X-ray spectroscopy
• electrodeposition
• electron energy loss spectroscopy
• voltammetry
• field-emission scanning electron microscopy