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Robust Porous TiN Layer for Improved Oxygen Evolution Reaction Performance

The poor reversibility and slow reaction kinetics of catalytic materials seriously hinder the industrialization process of proton exchange membrane (PEM) water electrolysis. It is necessary to develop high-performance and low-cost electrocatalysts to reduce the loss of reaction kinetics. In this stu...

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Detalles Bibliográficos
Autores principales: Liu, Gaoyang, Hou, Faguo, Wang, Xindong, Fang, Baizeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9653776/
https://www.ncbi.nlm.nih.gov/pubmed/36363193
http://dx.doi.org/10.3390/ma15217602
Descripción
Sumario:The poor reversibility and slow reaction kinetics of catalytic materials seriously hinder the industrialization process of proton exchange membrane (PEM) water electrolysis. It is necessary to develop high-performance and low-cost electrocatalysts to reduce the loss of reaction kinetics. In this study, a novel catalyst support featured with porous surface structure and good electronic conductivity was successfully prepared by surface modification via a thermal nitriding method under ammonia atmosphere. The morphology and composition characterization-confirmed that a TiN layer with granular porous structure and internal pore-like defects was established on the Ti sheet. Meanwhile, the conductivity measurements showed that the in-plane electronic conductivity of the as-developed material increased significantly to 120.8 S cm(−1). After IrO(x) was loaded on the prepared TiN-Ti support, better dispersion of the active phase IrO(x), lower ohmic resistance, and faster charge transfer resistance were verified, and accordingly, more accessible catalytic active sites on the catalytic interface were developed as revealed by the electrochemical characterizations. Compared with the IrO(x)/Ti, the as-obtained IrO(x)/TiN-Ti catalyst demonstrated remarkable electrocatalytic activity ([Formula: see text] = 302 mV) and superior stability (overpotential degradation rate: 0.067 mV h(−1)) probably due to the enhanced mass adsorption and transport, good dispersion of the supported active phase IrO(x), increased electronic conductivity and improved corrosion resistance provided by the TiN-Ti support.