Compositional and electronic reconstruction to co-incorporated NiOSO-NiMoO for boosting electrocatalytic overall water splitting/overall urea splitting reactions.

J Colloid Interface Sci

The Key Laboratory of Functional Molecular Solids, Ministry of Education, Key Laboratory of Electrochemical Clean Energy of Anhui Higher Education Institutes, Anhui Laboratory of Molecular-Based Materials, Center for Nano Science and Technology, College of Chemistry and Materials Science, Anhui Normal University, Wuhu 241000, China. Electronic address:

Published: January 2025

Herein, we grew in situ Co-incorporated NiOSO-NiMoO heterostructures on nickel foam (Co-NiSMoO/NF). The introduction of S and MoO into CoNi-ZIF precursor leads to the compositional and electronic reconstruction, resulting in the Co-NiSMoO/NF nanostructures. The attractive features in the morphology, composition, and electronic structure cooperatively endow them with high electrocatalytic performances. As a result, the Co-NiSMoO/NF nanostructures exhibit superior electrocatalytic performances to oxygen evolution, urea oxidation, and thus overall water/urea splitting reactions (OER/UOR/OWS/OUS). Specifically, the Co-NiSMoO/NF shows a high electrocatalytic OER activity, with low overpotentials of 172 mV@10 mA cm, 238 mV@20 mA cm, 278 mV@50 mA cm, 308 mV@100 mA cm in alkaline. For UOR, the overpotential is just as low as 1.318 V@10 mA cm, 1.330 V@20 mA cm, 1.346 V@50 mA cm, and 1.401 V@100 mA cm. Especially, the voltage of the record cell even drops to 1.446 V@10 mA cm to OUS. Furthermore, the Co-NiSMoO/NF electrocatalysts still stable to OER, UOR, and OUS even for up to 100 h. More importantly, we also realized H production in a green manner driven by solar. Under solar illumination on a solar panel, H production speed is even as high as 408 L h m.

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http://dx.doi.org/10.1016/j.jcis.2024.08.190DOI Listing

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