In:
Journal of Materials Chemistry A, Royal Society of Chemistry (RSC), Vol. 10, No. 48 ( 2022), p. 25692-25700
Abstract:
Iridium (Ir) single-atom catalysts (SACs) exhibit extraordinary advantages in the oxygen evolution reaction (OER) owing to their unique electronic structure and maximized atom utilization. However, further developments have met with bottlenecks due to the limited catalytic activity derived from the widely adopted adsorbate evolution mechanism (AEM) pathway in Ir SACs for OER. Herein, we report an efficient strategy to improve the intrinsic activity of Ir SACs by anchoring atomic Ir on an oxygen vacancy-modified CoNiO 2 support (Ir SA -V O -CoNiO 2 ), in which a more advanced lattice oxygen oxidation (LOM) pathway is constructed by activating lattice oxygen to participate in OER. Specifically, the synthesized CoNiO 2 support could provide the weak metal–oxygen bond and facilitate the movement and conversion of lattice oxygen. The oxygen vacancies provided abundant active sites for the adsorption of OH* and induced a substantial O 2p characteristic near the Fermi level for activating the lattice oxygen in CoNiO 2 . Moreover, the introduction of Ir atoms in the oxygen vacancies modulated CoNiO 2 results in the significant overlap between the Ir 5d and O 2p bands and constructed a stronger Ir–O covalent bond, which extremely facilitated the transformation from O–O to OO* for boosting the final O 2 evolution. Through the above-mentioned results, a more efficient LOM pathway in the single-atom Ir catalyst was constructed, and the as-synthesized Ir SA -V O -CoNiO 2 displayed outstanding OER performance with 10 mA cm −2 at a low overpotential of 183 mV and a high mass activity of 5 A mg −1 at the overpotential of 300 mV, significantly outperforming the reported catalysts. This work proposes an advanced channel to design efficient electrocatalysts for promising OER applications.
Type of Medium:
Online Resource
ISSN:
2050-7488
,
2050-7496
Language:
English
Publisher:
Royal Society of Chemistry (RSC)
Publication Date:
2022
detail.hit.zdb_id:
2702232-8
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