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Design and synthesis of Cu modified cobalt oxides with hollow polyhedral nanocages as efficient electrocatalytic and photocatalytic water oxidation catalysts

[Display omitted] •Hollow polyhedral nanocages Cu-ZIF-400, CuO/Co3O4 and Co3O4 catalysts are synthesized.•Three catalysts are obtained by modifying cobalt oxides with Cu using different methods.•All catalysts perform effective activities in electro/photocatalytic water oxidation.•Cu-ZIF-400 acts as...

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Bibliographic Details
Published in:Journal of catalysis 2017-08, Vol.352, p.246-255
Main Authors: Zhang, Yan, Zhou, Xichen, Zhang, Fuming, Tian, Tian, Ding, Yong, Gao, Hong
Format: Article
Language:English
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Summary:[Display omitted] •Hollow polyhedral nanocages Cu-ZIF-400, CuO/Co3O4 and Co3O4 catalysts are synthesized.•Three catalysts are obtained by modifying cobalt oxides with Cu using different methods.•All catalysts perform effective activities in electro/photocatalytic water oxidation.•Cu-ZIF-400 acts as the best electro/photocatalytic catalyst for oxygen evolution reaction. Cobalt oxides have been modified with Cu using different methods to obtain the catalysts of Cu-ZIF-400 (copper-doped cobalt oxide), CuO/Co3O4 and Co3O4 with identical morphology of hollow polyhedral nanocages. These catalysts were investigated simultaneously for electrocatalytic and photocatalytic water oxidation for the first time. Among them, Cu-ZIF-400 can act as the best electrochemical water oxidation catalyst with a low oxygen evolution reaction (OER) overpotential of 342mV at 10.0mAcm−2 in alkaline electrolyte. At the same time, a high turnover frequency (TOF) of 2.1×10−3s−1 per metal atom was obtained over Cu-ZIF-400 at neutral conditions, which is comparable to those documented cobalt based catalysts. The different performances of catalysts can be attributed to the different doping methods. We hypothesize that the electrophilic Cu2+ makes the Co more electron-drawing and facilitates the nucleophilic addition of water, which enhanced OER activity of Cu-ZIF-400 catalyst.
ISSN:0021-9517
1090-2694
DOI:10.1016/j.jcat.2017.05.020