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Activating Octahedral Center in Co-Doped NiFe 2 O 4 via Bridging Amorphous MoS x for Electrocatalytic Water Oxidation: A Case for e g Orbital Regulation in Spinel Oxide

Moderate e filling for octahedral metal cations (M ) is strongly correlated with the electrocatalytic water oxidation performance in the oxides system. Here, the e fillings of Ni and Fe in NiFe O -based spinel are controllably regulated by introducing an external radical of catalytically inactive Mo...

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Bibliographic Details
Published in:Small methods 2023-06, Vol.7 (6), p.e2201550
Main Authors: Yao, Lu, Wu, Xiaofeng, Zheng, Beining, Liu, Jinghai, Geng, Zhibin, Zhang, Yuan, Cai, Minmin, Shao, Zhiyu, Jiang, Mengpei, Zhang, Yaowen, Chen, Yu, Huang, Keke, Feng, Shouhua
Format: Article
Language:English
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Summary:Moderate e filling for octahedral metal cations (M ) is strongly correlated with the electrocatalytic water oxidation performance in the oxides system. Here, the e fillings of Ni and Fe in NiFe O -based spinel are controllably regulated by introducing an external radical of catalytically inactive MoS as an electron acceptor via a novel ultrasonic anchored pyrolysis strategy. The electron occupied in e orbit of M emigrates with the amount of MoS hanging on the apical of octahedral sites, and results in a salutary transition from high to medium e occupancy state, as confirmed by the X-ray absorption spectroscopy and X-ray photoelectron spectroscopy. In addition, benefiting from the abundant unsaturated S atoms in amorphous MoS , the M at the surface furthest activates and consequently shows a superior water oxidation performance. Density functional theory also reveals that the e fillings of Ni and Fe decrease to 1.4 and 1.2 after MoS modification, which can effectively reduce the free energy of the OOH* intermediates in the oxygen evolution reaction process. This work opens an avenue for further releasing the electrocatalytic activity of octahedral sites through bridging external phases with rational electron-capturing/donating capability.
ISSN:2366-9608
2366-9608
DOI:10.1002/smtd.202201550