TY  - JOUR
AU  - Obradovic, Maja D.
AU  - Balanč, Bojana
AU  - Lačnjevac, Uroš C.
AU  - Gojković, Snežana Lj.
PY  - 2021
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4928
AB  - Hydrated iridiumoxyhydroxide (IrOx) films were electrochemically deposited from an alkaline oxalic solution at constant anodic potentials and by applying a potential cycling protocol, in both cases with variation of the electrodeposition time. FromUV-vis spetroscopy of the solution for the deposition and their characterization it was concluded that a mixture of Ir(III)/Ir(IV) monomers participates in the deposition of IrOx film. X-ray photoelectron spectroscopy (XPS) of IrOx films indicated that both types of films contained hydrated Ir(IV) hydroxide as the dominant species, but in the film deposited by potential cycling the presence of the additional Ir(III) species was evident. The scanning electon microscopy (SEM) analysis of the surface morphology revealed that films deposited by potential cycling were more uniform than the films deposited at a constant potential. The amount of electrochemically active Ir-species on the surface of deposited IrOx films was estimated from the voltammetric charge of the Ir(III)/Ir(IV) transition. Depending on the film electrodeposition parameters, the values between 15 and 1080 nmol cm-2 were obtained. The electrochemically active surface area (ECSA) of IrOx films was calculated from cyclic voltammetry and electrochemical impedance spectroscopy (EIS) measurements and ranged from 3 to 131 cm(2) per 1 cm(2) of geometric surface area for various films. The activity and stability of IrOx films toward oxygen evolution reaction (OER) was investigated in 0.5 M H2SO4 solution under potentiostatic conditions. The intrinsic activity, stated as turnover frequency and specific current density normalized per ECSA, showed that the OER activity of IrOx films deposited by potential cycling are up to two and a half times higher than the activity of films deposited at a constant anodic potential. Potentiostatic stability test showed a decrease in OER current over time for both type of the films. Determination of ECSA, the amount of electroactive Ir species, XPS spectrum and SEM imaging after the test indicated that the decrease in OER activity was caused by partial dissolution and delamination of the film as well as by oxidation of highly active hydroxide Ir(III) species.
T2  - Journal of Electroanalytical Chemistry
T1  - Electrochemically deposited iridium-oxide: Estimation of intrinsic activity and stability in oxygen evolution in acid solution
VL  - 881
DO  - 10.1016/j.jelechem.2020.114944
ER  - 

@article{
author = "Obradovic, Maja D. and Balanč, Bojana and Lačnjevac, Uroš C. and Gojković, Snežana Lj.",
year = "2021",
abstract = "Hydrated iridiumoxyhydroxide (IrOx) films were electrochemically deposited from an alkaline oxalic solution at constant anodic potentials and by applying a potential cycling protocol, in both cases with variation of the electrodeposition time. FromUV-vis spetroscopy of the solution for the deposition and their characterization it was concluded that a mixture of Ir(III)/Ir(IV) monomers participates in the deposition of IrOx film. X-ray photoelectron spectroscopy (XPS) of IrOx films indicated that both types of films contained hydrated Ir(IV) hydroxide as the dominant species, but in the film deposited by potential cycling the presence of the additional Ir(III) species was evident. The scanning electon microscopy (SEM) analysis of the surface morphology revealed that films deposited by potential cycling were more uniform than the films deposited at a constant potential. The amount of electrochemically active Ir-species on the surface of deposited IrOx films was estimated from the voltammetric charge of the Ir(III)/Ir(IV) transition. Depending on the film electrodeposition parameters, the values between 15 and 1080 nmol cm-2 were obtained. The electrochemically active surface area (ECSA) of IrOx films was calculated from cyclic voltammetry and electrochemical impedance spectroscopy (EIS) measurements and ranged from 3 to 131 cm(2) per 1 cm(2) of geometric surface area for various films. The activity and stability of IrOx films toward oxygen evolution reaction (OER) was investigated in 0.5 M H2SO4 solution under potentiostatic conditions. The intrinsic activity, stated as turnover frequency and specific current density normalized per ECSA, showed that the OER activity of IrOx films deposited by potential cycling are up to two and a half times higher than the activity of films deposited at a constant anodic potential. Potentiostatic stability test showed a decrease in OER current over time for both type of the films. Determination of ECSA, the amount of electroactive Ir species, XPS spectrum and SEM imaging after the test indicated that the decrease in OER activity was caused by partial dissolution and delamination of the film as well as by oxidation of highly active hydroxide Ir(III) species.",
journal = "Journal of Electroanalytical Chemistry",
title = "Electrochemically deposited iridium-oxide: Estimation of intrinsic activity and stability in oxygen evolution in acid solution",
volume = "881",
doi = "10.1016/j.jelechem.2020.114944"
}

Obradovic, M. D., Balanč, B., Lačnjevac, U. C.,& Gojković, S. Lj.. (2021). Electrochemically deposited iridium-oxide: Estimation of intrinsic activity and stability in oxygen evolution in acid solution. in Journal of Electroanalytical Chemistry, 881.
https://doi.org/10.1016/j.jelechem.2020.114944

Obradovic MD, Balanč B, Lačnjevac UC, Gojković SL. Electrochemically deposited iridium-oxide: Estimation of intrinsic activity and stability in oxygen evolution in acid solution. in Journal of Electroanalytical Chemistry. 2021;881.
doi:10.1016/j.jelechem.2020.114944 .

Obradovic, Maja D., Balanč, Bojana, Lačnjevac, Uroš C., Gojković, Snežana Lj., "Electrochemically deposited iridium-oxide: Estimation of intrinsic activity and stability in oxygen evolution in acid solution" in Journal of Electroanalytical Chemistry, 881 (2021),
https://doi.org/10.1016/j.jelechem.2020.114944 . .