4.6 Article

The Nucleation Rate of Single O2 Nanobubbles at Pt Nanoelectrodes

Journal

LANGMUIR
Volume 34, Issue 25, Pages 7309-7318

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.langmuir.8b01372

Keywords

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Funding

  1. Netherlands Centre for Multiscale Catalytic Energy Conversion (MCEC)
  2. Ministry of Education, Culture and Science of the government of The Netherlands
  3. Office of Naval Research [N00014-16-1-2541]

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Nanobubble nucleation is a problem that affects efficiency in electrocatalytic reactions since those bubbles can block the surface of the catalytic sites. In this article, we focus on the nucleation rate of O-2 nanobubbles resulting from the electrooxidation of H2O2 at Pt disk nanoelectrodes. Bubbles form almost instantaneously when a critical peak current, i(nb)(P), is applied, but for lower currents, bubble nucleation is a stochastic process in which the nucleation (induction) time, t(ind), dramatically decreases as the applied current approaches i(nb)(P), a consequence of the local supersaturation level, zeta, increasing at high currents. Here, by applying different currents below i(nb)(P) nanobubbles take some time to nucleate and block the surface of the Pt electrode at which the reaction occurs, providing a means to measure the stochastic t(ind). We study in detail the different conditions in which nanobubbles appear, concluding that the electrode surface needs to be preconditioned to achieve reproducible results. We also measure the activation energy for bubble nucleation, E-a, which varies in the range from (6 to 30)kT, and assuming a spherically cap-shaped nanobubble nucleus, we determine the footprint diameter L = 8-15 nm, the contact angle to the electrode surface theta = 135-155 degrees, and the number of O-2 molecules contained in the nucleus (50 to 900 molecules).

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