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Accelerated Reconstruction from Co-ZIF‑L to CoOOH via a Tailored Electronic Structure of Cobalt for Oxygen Evolution
The Oxygen Evolution Reaction (OER) encounters an insurmountable kinetic bottleneck in water electrolysis due to the complex four-electron transfer process, while modulating the oxidation states of active sites holds promise for enhancing the OER performance. Here, we successfully prepare cobalt-bas...
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Published in: | Industrial & engineering chemistry research 2024-05, Vol.63 (18), p.8142-8150 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | The Oxygen Evolution Reaction (OER) encounters an insurmountable kinetic bottleneck in water electrolysis due to the complex four-electron transfer process, while modulating the oxidation states of active sites holds promise for enhancing the OER performance. Here, we successfully prepare cobalt-based zeolitic imidazolate framework Co-ZIF-L on carbon cloth with high-valence Co sites (O-ZIF-CC) through a facile oxidation strategy by heat treatment under an air atmosphere and achieve rapid reconstruction from Co-ZIF-L to CoOOH during OER. The O-ZIF-CC, as an active MOF-based catalyst, exhibits a low overpotential (283 mV at 10 mA cm–2). The excellent electrocatalytic activity of the O-ZIF-CC can be ascribed to the introduction of high-valence Co sites, facilitating reconstruction to generate CoOOH at low potentials. This work provides a feasible approach for understanding the optimization of the performance of MOF-based electrocatalysts through valence-state tuning. |
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ISSN: | 0888-5885 1520-5045 1520-5045 |
DOI: | 10.1021/acs.iecr.4c00491 |