The corona of a surface bubble promotes electrochemical reactions
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Authors
Vogel, Yan B.
Evans, Cameron W.
Belotti, Mattia
Xu, Longkun
Russell, Isabella
Yu, Li-Juan
Fung, Alfred K. K.
Hill, Nicholas
Darwish, Nadim
Gonçales, Vinicius R.
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Nature Publishing Group UK
Abstract
The evolution of gaseous products is a feature common to several electrochemical processes,
often resulting in bubbles adhering to the electrode’s surface. Adherent bubbles reduce the
electrode active area, and are therefore generally treated as electrochemically inert entities.
Here, we show that this general assumption does not hold for gas bubbles masking anodes
operating in water. By means of imaging electrochemiluminescent systems, and by studying
the anisotropy of polymer growth around bubbles, we demonstrate that gas cavities adhering
to an electrode surface initiate the oxidation of water-soluble species more effectively than
electrode areas free of bubbles. The corona of a bubble accumulates hydroxide anions,
unbalanced by cations, a phenomenon which causes the oxidation of hydroxide ions to
hydroxyl radicals to occur at potentials at least 0.7 V below redox tabled values. The downhill
shift of the hydroxide oxidation at the corona of the bubble is likely to be a general
mechanism involved in the initiation of heterogeneous electrochemical reactions in water,
and could be harnessed in chemical synthesis.
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Nature Communications
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Open Access
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