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Research Article

Co3O4 Nanocrystals on Single-Walled Carbon Nanotubes as a Highly Efficient Oxygen-Evolving Catalyst

Jian Wu1Yan Xue1Xin Yan1Wensheng Yan2Qingmei Cheng1Yi Xie1( )
Hefei National Laboratory for Physical Sciences at MicroscaleUniversity of Science & Technology of ChinaHefeiAnhui230026China
National Synchrotron Radiation LaboratoryUniversity of Science & Technology of ChinaHefeiAnhui230029China
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Abstract

The efficient catalytic oxidation of water to dioxygen is envisioned to play an important role in solar fuel production and artificial photosynthetic systems. Despite tremendous efforts, the development of oxygen evolution reaction (OER) catalysts with high activity and low cost under mild conditions remains a great challenge. In this work, we develop a hybrid consisting of Co3O4 nanocrystals supported on single-walled carbon nanotubes (SWNTs) via a simple self-assembly approach. A Co3O4/SWNTs hybrid electrode for the OER exhibits much enhanced catalytic activity as well as superior stability under neutral and alkaline conditions compared with bare Co3O4, which only performs well in alkaline solution. Moreover, the turnover frequency for the OER exhibited by Co3O4/SWNTs in neutral water is higher than for bare Co3O4 catalysts. Synergetic chemical coupling effects between Co3O4 nanocrystals and SWNTs, revealed by the synchrotron X-ray absorption near edge structure (XANES) technique, can be regarded as contributing to the activity, cycling stability and stable operation under neutral conditions. Use of the SWNTs as an immobilization matrix substantially increases the active electrode surface area, enhances the durability of catalysts under neutral conditions and improves the electronic coupling between Co redox-active sites of Co3O4 and the electrode surface.

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Nano Research
Pages 521-530

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Cite this article:
Wu J, Xue Y, Yan X, et al. Co3O4 Nanocrystals on Single-Walled Carbon Nanotubes as a Highly Efficient Oxygen-Evolving Catalyst. Nano Research, 2012, 5(8): 521-530. https://doi.org/10.1007/s12274-012-0237-y

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Received: 18 February 2012
Revised: 03 June 2012
Accepted: 05 June 2012
Published: 22 July 2012
© Tsinghua University Press and Springer-Verlag GmbH Germany, part of Springer Nature 2012