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Stabilizing the High Spin Cobalt Atoms by Local Magnetic Asymmetry in p-Block Metals-Doped Spinel MnCo2O4 Catalysts
Shuyun Lou1,2, Guojun Wen1,2, Shike Xu3
1State Key Laboratory of Chemistry for NBC Hazards Protection, College of Chemistry, Fuzhou University, Fuzhou, 350116, P. R. China.
Abstract:
Spinel MnCo2O4 (MCO) is often used for electrocatalytic oxygen reduction reaction (eORR), limited kinetically by the electronic spin state of surface cobalt (Co) centers. In this work, the rate-determining step of eORR is unlocked by doping p-block metals, including Ga, In, and Pb, into MCO catalysts to stabilize the high-spin state of surface octahedral Co atoms, where the high-spin electrons are rapidly injected into triplet O2 adsorbates. The optimal Pb-doped MCO catalyst (denoted as 0.2MCPO) as an air electrode is used to setup a solid oxide fuel cell (SOFC) device, achieving a significantly-enhanced peak power density of 1.53 W cm-2 and remarkable stability over 210 h. The M─2O─Co covalencies make the high-spin state of surface octahedral Co atoms more stable by the p-d orbital coupling mechanism, and thus boost kinetically the electron transfer from surface Co sites to O2 adsorbates. A combination of experimental and theoretical analysis reveals that the stable high-spin state of Co atoms enhances O2 adsorption and activation, lowering the energy barriers for the homolytic cleavage of O2 into two *O atoms. These findings offer fundamental insights into spin-selected electrocatalysis for ORR and a general guidance to construction of high-performance SOFC devices for energy conversion and storage.
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