Issue 28, 2023

Metal-support interactions alter the active species on IrOx for electrocatalytic water oxidation

Abstract

Constructing metal-support interaction (MSI) is a strategy of wide interest to promote the electrocatalytic performance of oxygen evolution reaction (OER). However, studies helping to understand the electrocatalytic behavior of reactive centers affected by the metal support and investigations to guide the construction of catalysts based on MSI are scarce. In situ surface-enhanced Raman spectroscopy (SERS) provides spectral evidence of reactive intermediates and information on the structural evolution of catalysts, which can help investigate the reaction pathway of catalysts. In this work, Au@MnO2-IrOx core–shell nanoparticles (NPs), possessing a specific nanostructure of highly dispersed IrOx clusters on amorphous MnO2 shells, were prepared by a simple method under ambient conditions and exhibited a low overpotential of 230 mV to reach the current density of 10 mA cm−2, therefore outperforming the traditional Ir catalysts. The oxidation of Ir4+ and adsorption of *O on IrOx at a low potential were revealed by in situ SERS, which indicated the pre-activation of Ir centers and the facilitated formation of superoxide species: *O–O. Combined with density functional theory (DFT) calculations, we show that the MnO2 substrate optimizes binding energies of intermediates on IrOx, promoting O–O coupling and improving the OER rate. This work provides a strategy for utilizing in situ spectroscopy to investigate the OER mechanism and understand the electrocatalytic behavior impacted by MSI.

Graphical abstract: Metal-support interactions alter the active species on IrOx for electrocatalytic water oxidation

Supplementary files

Article information

Article type
Paper
Submitted
16 رمضان 1444
Accepted
05 ذو الحجة 1444
First published
06 ذو الحجة 1444

J. Mater. Chem. A, 2023,11, 15204-15210

Metal-support interactions alter the active species on IrOx for electrocatalytic water oxidation

G. Xu, M. Yue, Z. Qian, Z. Du, X. Xie, W. Chen, Y. Zhang and J. Li, J. Mater. Chem. A, 2023, 11, 15204 DOI: 10.1039/D3TA02115G

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