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Although polymer electrolyte membrane fuel cells (PEMFCs) have received broad attention due to their virtually zero emission, high power density, and high efficiency, at present the limited stability of the electrocatalysts used in PEMFCs is a critical limitation to their large-scale commercialization. As a type of popularly used electrocatalyst material, carbon black supported platinum (Pt/C)—although highly efficient—undergoes corrosion of carbon, Pt dissolution, Ostwald ripening, and aggregation of Pt nanoparticles (NPs) under harsh chemical and electrochemical oxidation conditions, which results in performance degradation of the electrocatalysts. In order to overcome these disadvantages, many groups have tried to improve the carbon support materials on which Pt is loaded. It has been found that some novel carbon nanomaterials and noncarbon materials with high surface areas, sufficient anchoring sites, high electrical conductivities, and high oxidation resistance under the strongly oxidizing condition in PEMFCs are ideal alternative supports. This review highlights the following aspects: (i) Recent advances in using novel carbon nanomaterials and noncarbon support materials to enhance the long-term durability of electrocatalysts; (ii) solutions to improve the electrical conductivity, surface area, and the strong interaction between metal and supports; and (iii) the synergistic effects in hybrid supports which help improve the stability of electrocatalysts.

Publication history
Copyright
Acknowledgements

Publication history

Received: 15 September 2014
Revised: 12 December 2014
Accepted: 14 December 2014
Published: 06 January 2015
Issue date: February 2015

Copyright

© Tsinghua University Press and Springer-Verlag Berlin Heidelberg 2014

Acknowledgements

Acknowledgements

Our research was financially sponsored by National Basic Research Program of China (Grant Nos. 2012CB215500 and 2012CB720300) and the National Natural Science Foundation of China (Grant Nos. 20936008, 21176271, 21276291, 21376284, and 21436003).

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