open access publication

Preprint, 2024

Electrodeposition of tunable Cu-Ag nanostructures in a deep eutectic solvent

ChemRxiv, ISSN 2573-2293, 10.26434/chemrxiv-2024-lckq9-v2

Contributors

Plaza-Mayoral, Elena 0000-0001-7208-7940 [1] Dalby, Kim Nicole 0000-0001-6048-3583 [2] Falsig, Hanne 0000-0002-2474-4093 [2] Chorkendorff, I B 0000-0003-2738-0325 [3] Sebastián-Pascual, Paula 0000-0001-7985-0750 [1] Escudero-Escribano, Marı A 0000-0002-6432-3015 [4] [5]

Affiliations

  1. [1] University of Copenhagen
  2. [NORA names: KU University of Copenhagen; University; Denmark; Europe, EU; Nordic; OECD];
  3. [2] Haldor Topsoe (Denmark)
  4. [NORA names: Topsoe; Private Research; Denmark; Europe, EU; Nordic; OECD];
  5. [3] Technical University of Denmark
  6. [NORA names: DTU Technical University of Denmark; University; Denmark; Europe, EU; Nordic; OECD];
  7. [4] Catalan Institute of Nanoscience and Nanotechnology (ICN2), CSIC, Barcelona Institute of Science and Technology, UAB Campus, 08193 Bellaterra, Barcelona, Spain
  8. [NORA names: Spain; Europe, EU; OECD];
  9. [5] Institució Catalana de Recerca i Estudis Avançats
  10. [NORA names: Spain; Europe, EU; OECD]

Abstract

The green transition requires the preparation of clean, inexpensive, and sustainable strategies to prepare controllable bimetallic and multimetallic nanostructures. Cu-Ag nanostructures, for example, are promising bimetallic catalysts for different electrocatalytic reactions such as carbon monoxide and carbon dioxide reduction. In this work, we present the one-step preparation method of electrodeposited Cu-Ag with tunable composition and morphology from choline chloride plus urea deep eutectic solvent (DES), a non-toxic and green DES. We have assessed how different electrodeposition parameters affect the morphology and composition of our nanostructures. We combine electrochemical methods with ex-situ scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS) and X-ray photoelectron spectroscopy (XPS) to characterize the nanostructures. We have estimated the electrochemically active surface area (ECSA) and roughness factor (R) by lead underpotential deposition (UPD). The copper/silver ratio in the electrodeposited nanostructures is highly sensitive to the applied potential, bath composition, and loading. We observed that silver-rich nanostructures were less adherent whereas the increase in copper content led to more stable and homogenous films with disperse rounded nanostructures with tiny spikes. These spikes were more stable when the deposition rate was fast enough and the molar ratio of Cu and Ag no greater than approximately two to one.

Keywords

Ag, Cu-Ag, X-ray, X-ray photoelectron spectroscopy, X-ray spectroscopy, active surface area, area, bath, bath composition, bimetallic catalysts, carbon, carbon dioxide reduction, carbon monoxide, catalyst, chloride, choline, choline chloride, composition, content, copper, copper content, copper/silver, copper/silver ratios, deep eutectic solvents, deposition, deposition rate, dispersive X-ray spectroscopy, electrocatalytic reactions, electrochemical methods, electrochemically, electrochemically active surface area, electrodeposited nanostructures, electrodeposition, electrodeposition parameters, electron microscopy, energy, energy dispersive X-ray spectroscopy, eutectic solvents, ex situ scanning electron microscopy, factors, films, green deep eutectic solvent, green transition, homogeneous films, increase, lead underpotential deposition, load, method, microscopy, molar ratio, molar ratio of Cu, monoxide, morphology, multimetallic nanostructures, nanostructures, non-toxic, one-step preparation method, parameters, photoelectron spectroscopy, potential, preparation, rate, ratio, ratio of Cu, reaction, reduction, roughness, roughness factor, scanning electron microscopy, solvent, spectroscopy, spikes, surface area, transition, tunable composition, underpotential deposition, urea, urea deep eutectic solvent

Funders

  • The Velux Foundations

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