4.8 Article

Stabilization effects in binary colloidal Cu and Ag nanoparticle electrodes under electrochemical CO2 reduction conditions

Journal

NANOSCALE
Volume 13, Issue 9, Pages 4835-4844

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0nr09040a

Keywords

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Funding

  1. Strategic UU-TU/e Alliance project 'Joint Centre for Chemergy Research'
  2. European Research Council (ERC) [815128 REALNANO]
  3. University of Antwerp Research fund (BOF)

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Nanoparticle modified electrodes are an attractive way to tailor efficient carbon dioxide reduction catalysts, but the restructuring and sintering processes of nanoparticles under electrochemical reaction conditions can hinder their widespread application. By colloidally synthesizing and utilizing metallic copper and silver nanoparticles, the stabilization effect between Cu and Ag nanoparticles was observed, leading to suppressed sintering and tunable selectivity in CO2 reduction reactions. This stabilization effect is attributed to the positive enthalpies of Cu-Ag solid solutions, enabling the design and fabrication of durable CO2 reduction nanocatalysts.
Nanoparticle modified electrodes constitute an attractive way to tailor-make efficient carbon dioxide (CO2) reduction catalysts. However, the restructuring and sintering processes of nanoparticles under electrochemical reaction conditions not only impedes the widespread application of nanoparticle catalysts, but also misleads the interpretation of the selectivity of the nanocatalysts. Here, we colloidally synthesized metallic copper (Cu) and silver (Ag) nanoparticles with a narrow size distribution (<10%) and utilized them in electrochemical CO2 reduction reactions. Monometallic Cu and Ag nanoparticle electrodes showed severe nanoparticle sintering already at low overpotential of -0.8 V vs. RHE, as evidenced by ex situ SEM investigations, and potential-dependent variations in product selectivity that resemble bulk Cu (14% for ethylene at -1.3 V vs. RHE) and Ag (69% for carbon monoxide at -1.0 V vs. RHE). However, by co-deposition of Cu and Ag nanoparticles, a nanoparticle stabilization effect was observed between Cu and Ag, and the sintering process was greatly suppressed at CO2 reducing potentials (-0.8 V vs. RHE). Furthermore, by varying the Cu/Ag nanoparticle ratio, the CO2 reduction reaction (CO2RR) selectivity towards methane (maximum of 20.6% for dense Cu-2.5-Ag-1 electrodes) and C-2 products (maximum of 15.7% for dense Cu-1-Ag-1 electrodes) can be tuned, which is attributed to a synergistic effect between neighbouring Ag and Cu nanoparticles. We attribute the stabilization of the nanoparticles to the positive enthalpies of Cu-Ag solid solutions, which prevents the dissolution-redeposition induced particle growth under CO2RR conditions. The observed nanoparticle stabilization effect enables the design and fabrication of active CO2 reduction nanocatalysts with high durability.

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