Kinetic Insights into Glycerol Electrooxidation on Nickel: Current-Dependent Product Distribution and Reaction Mechanism
Authors/Creators
- 1. Institute of Advanced Materials (INAM), Universitat Jaume I, 12006 Castelló, Spain
Description
## FILE DESCRIPTION
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### Figure 1
- Fig1a.txt : Cyclic voltammetry of a Ni-based electrode in 0.1 M LiOH and 50 mM glycerol, measured at 5 mV s^-1.
- Fig1b.txt : IS spectra obtained at 1.50 V vs RHE in 0.1 M LiOH and 0.1 M LiOH + 50 mM glycerol.
- Fig1c.txt : Chronopotentiometric curves at 1 mA cm^-2, 3 mA cm^-2, 5 mA cm^-2 during 2 hours in 0.1 M LiOH + 50 mM glycerol.
### Figure 2
- Fig2a.txt : Faradaic Efficiencies for Glycerol oxidation electrolysis at 1 mA cm^-2.
- Fig2b.txt : Faradaic Efficiencies for Glycerol oxidation electrolysis at 3 mA cm^-2.
- Fig2c.txt : Faradaic Efficiencies for Glycerol oxidation electrolysis at 5 mA cm^-2.
- Fig2d.txt : Faradaic Efficiencies for Glycerol oxidation electrolysis at 10 mA cm^-2.
- Fig2e.txt : Concentration of reaction products vs. time plots during glycerol oxidation (50 mM) in 0.1 M LiOH at 1 mA cm^-2.
- Fig2f.txt : Concentration of reaction products vs. time plots during glycerol oxidation (50 mM) in 0.1 M LiOH at 3 mA cm^-2.
- Fig2g.txt : Concentration of reaction products vs. time plots during glycerol oxidation (50 mM) in 0.1 M LiOH at 5 mA cm^-2.
- Fig2h.txt : Concentration of reaction products vs. time plots during glycerol oxidation (50 mM) in 0.1 M LiOH at 10 mA cm^-2.
### Figure 3
- Fig3a.txt : Rate constant comparison at varying current densities applied for the formation of formate, glycolate, glycerate, tartronate and oxalate with its error bar.
### Figure 4
- Fig4a.txt : Differential optical density (m∆O.D) taken at the maximum absorption peak as a function of potential applied in a solution of 0.1 M LiOH and LiOH 0.1 M + 50 mM glycerol in different regions (capacitive, NiOOH formation and GEOR and OER).
- Fig4b.txt : Rate law plot for glycerol and LiOH considering current density as a function of the normalized differential absorption (m∆O.D).
### Figure S3
- FigS3.txt : X-ray diffraction (XRD) analysis
### Figure S4
- FigS4a.txt : Cyclic Voltammetries in different electrolytes.
### Figure S5
- FigS5a.txt : Faradaic Efficiencies for Glycerol oxidation electrolysis at 1.53 V vs RHE.
- FigS5b.txt : Faradaic Efficiencies for Glycerol oxidation electrolysis at 1.62 V vs RHE.
- FigS5c.txt : Faradaic Efficiencies for Glycerol oxidation electrolysis at 1.78 V vs RHE.
### Figure S6
- FigS6a.txt : pH measurement near to the surface of the electrode and in the bulk of the solution every five minutes at 1 mA cm^-2.
- FigS6b.txt : pH measurement near to the surface of the electrode and in the bulk of the solution every five minutes at 3 mA cm^-2.
- FigS6c.txt : pH measurement near to the surface of the electrode and in the bulk of the solution every five minutes at 5 mA cm^-2.
### Figure S7
- FigS7a.txt : UV-Vis absorbance spectra as a function of applied potentials in 0.1 M LiOH.
- FigS7b.txt : Chronoamperometry measurement without glycerol.
- FigS7c.txt : UV-Vis absorbance spectra as a function of applied potentials in 0.1 M LiOH + 50 mM glycerol.
- FigS8d.txt : Chronoamperometry measurement with glycerol.
### Figure S8
- FigS8a.txt : Differential UV-Vis spectra of pre-catalytic (species formed in capacitive and NiOOH formation region) in 0.1 M LiOH.
- FigS8b.txt : Differential UV-Vis spectra of catalytic species (formed in OER and GEOR region) in 0.1 M LiOH.
- FigS8c.txt : Differential UV-Vis spectra of pre-catalytic species in 0.1 M LiOH + 50 mM glycerol.
- FigS8d.txt : Differential UV-Vis spectra of catalytic species in 0.1 M LiOH + 50 mM glycerol.
- FigS8e.txt : Steady state J-V curve with the onset for OER (Oxygen Evolution Reaction) and GEOR (Glycerol Electrooxidation Reaction) indicated.
### Figure S9
- FigS9.txt : Rate law plot for glycerol and LiOH considering current density (j) as a function of the normalized differential absorption (m∆O.D).
Files
Replication package.zip
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Additional details
Funding
- Ministerio de Ciencia, Innovación y Universidades
- DESARROLLO DE SISTEMAS ELECTROCATALÍTICOS INTEGRADOS PARA LA SÍNTESIS DE PRODUCTOS QUÍMICOS DE ALTO VALOR AÑADIDO PID2020-116093RB-C41
- Generalitat Valenciana
- Subvencions per a la contractació de personal investigador en fase postdoctoral APOSTD/2021/251
- Generalitat Valenciana
- MATERIALES FUNCIONALES PARA LA PRODUCCIÓN Y ALMACENAMIENTO EFICIENTE DE HIDRÓGENO VERDE MFA/2022/043
Dates
- Created
-
2024-08-26