Pt(111) - 0.1 M CsF + HClO4
echemdb identifier: briega-martos_2021_cation_48_f1cs_green
tags:
BCV
A cyclic voltammogramm for Pt(111) recorded in 0.1 M CsF + HClO4 at a scan rate of 50.0 \(\mathrm{mV\,s^{-1}}\) from Figure 1Cs in V. Briega-Martos et al. Cation Effects on Interfacial Water Structure and Hydrogen Peroxide Reduction on Pt (111). ACS Measurement Science Au, 1(2):48–55, 2021.
Further information
The figure shows digitized data.
Preparation procedure not available.
Metadata
Details on the electrochemical system (yaml)
electrodes:
- crystallographic orientation: poly
function: counter electrode
material: Pt
name: CE
shape:
type: coiled wire
- function: reference electrode
name: REF
type: RHE
- crystallographic orientation: '111'
function: working electrode
geometric electrolyte contact area:
unit: 1 / cm2
material: Pt
name: WE
shape:
diameter:
unit: mm
value: 2
height:
unit: mm
type: bead
electrolyte:
components:
- concentration:
unit: mol / l
value: 0.1
name: CsF
source:
purity:
unit: pct
value: 99.99
supplier: Alfa Aesar Puratronic
type: salt
- name: water
source:
quality: ultrapure water
type: solvent
- concentration:
unit: mol / l
name: HClO4
source:
supplier: Merck
type: acid
ph:
value: 2.3
temperature:
unit: K
value: 298.15
type: aqueous
type: electrochemical
Citation key (bibtex)
@article{briega_martos_2021_cation_48,
author = "Briega-Martos, Valent{\'\i}n and Sarabia, Francisco J and Climent, V{\'\i}ctor and Herrero, Enrique and Feliu, Juan M",
title = "Cation Effects on Interfacial Water Structure and Hydrogen Peroxide Reduction on Pt (111)",
journal = "ACS Measurement Science Au",
year = "2021",
volume = "1",
number = "2",
pages = "48--55",
publisher = "ACS Publications",
abstract = "The interface between the Pt(111) surface and several MeF/HClO4 (Me+ = Li+, Na+, or Cs+) aqueous electrolytes is investigated by means of cyclic voltammetry and laser-induced temperature jump experiments. Results point out that the effect of the electrolyte on the interfacial water structure is different depending on the nature of the metal alkali cation, with the values of the potential of maximum entropy (pme) following the order pme (Li+) < pme (Na+) < pme (Cs+). In addition, the hydrogen peroxide reduction reaction is studied under these conditions. This reaction is inhibited at low potentials as a consequence of the build up of negative charges on the electrode surface. The potential where this inhibition takes place (Einhibition) follows the same trend as the pme. These results evidence that the activity of an electrocatalytic reaction can depend to great extent on the structure of the interfacial water adlayer and that the latter can be modulated by the nature of the alkali metal cation."
}
Details about the original figure in the publicaton (yaml).
comment: ''
fields:
- name: E
orientation: x
reference: SHE
type: number
unit: V
- name: j
orientation: y
type: number
unit: uA / cm2
measurement type: CV
scan rate:
unit: mV / s
value: 50.0
simultaneous measurements: []
type: digitized
version: 1
Details about the curation process of this entry (yaml).
process:
- date: '2021-09-21'
name: Nicolas Hoermann
orcid: https://orcid.org/0000-0001-6944-5575
role: curator
- date: '2022-01-21'
name: Albert Engstfeld
orcid: https://orcid.org/0000-0002-9686-3948
role: reviewer