AI Article Synopsis

  • Investigated the interaction between gold (Au) and polydimethylsiloxane (PDMS) to understand how static charges are generated and how they facilitate redox reactions in water, potentially aiding in energy harvesting.
  • Used Kelvin probe force microscopy (KPFM) to observe that positive static charges accumulate on contact areas of Au with PDMS; water exposure alters the polarity of these charges.
  • Electrochemical experiments, such as open circuit potential and stripping voltammetry, showed that charged Au can reduce reactants in water through reducing radicals, rather than merely discharging static electricity.

Article Abstract

We investigated the static charge generation by contact electrification between Au and polydimethylsiloxane (PDMS) and the redox reaction by the static charge in the aqueous phase, to reveal the mechanism of contact electrification and redox reaction which may be applied to mechanical-to-chemical energy harvesting. First, the static charge distribution on the equipotential Au was probed through Kelvin probe force microscopy (KPFM) in air after the contact with patterned PDMS. Positive charges are localized on the contact areas indicating the ion migration while the polarity becomes negative after water contact. Second, the redox reaction by the charged Au was electrochemically monitored using open circuit potential (OCP), stripping voltammetry, and copper underpotential deposition (UPD). All electrochemical experiments consistently resulted in the reduction of the reactant by the charged Au within the highly dielectric water media. We concluded that the reduction is not driven by the discharge of static charge on Au but by reducing radicals.

Download full-text PDF

Source
http://dx.doi.org/10.1021/jacs.8b07297DOI Listing

Publication Analysis

Top Keywords

redox reaction
20
static charge
16
contact electrification
12
electrification polydimethylsiloxane
8
contact
6
static
5
redox
5
reaction
5
charge
5
static electricity
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!