The nucleation rate of single O2 nanobubble at Pt nanoelectrodes Articles uri icon

authors

  • MORENO SOTO, ALVARO
  • GERMAN, SEAN R.
  • REN, HANG
  • VAN DER MEER, DEVARAJ
  • LOHSE, DETLEF
  • EDWARDS, MARTIN A.
  • WHITE, HENRY S.

publication date

  • June 2018

start page

  • 7309

end page

  • 7318

issue

  • 25

volume

  • 34

International Standard Serial Number (ISSN)

  • 0743-7463

Electronic International Standard Serial Number (EISSN)

  • 1520-5827

abstract

  • 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 O2 nanobubbles resulting from the electrooxidation of H2O2 at Pt disk nanoelectrodes. Bubbles form almost instantaneously when a critical peak current, inbp, is applied, but for lower currents, bubble nucleation is a stochastic process in which the nucleation (induction) time, tind, dramatically decreases as the applied current approaches inbp, a consequence of the local supersaturation level, ζ, increasing at high currents. Here, by applying different currents below inbp, 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 tind. 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, Ea, 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 θ = 135–155°, and the number of O2 molecules contained in the nucleus (50 to 900 molecules).

subjects

  • Industrial Engineering
  • Materials science and engineering