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Pt supported on highly graphitized lace-like carbon for methanol electrooxidation

  • Dingsheng Yuan
  • , Shaozao Tan
  • , Yingliang Liu
  • , Jianghua Zeng
  • , Fengping Hu
  • , Xin Wang
  • , Peikang Shen

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

Abstract

A simple solvothermal method has been used to synthesize highly graphitized lace-like carbon (GLC) using ethanol as the carbon source and Mg as reducing agent. The GLC is characterized by transmission electron microscopy, X-ray diffraction, N2 adsorption, Raman spectroscopy and electrochemical techniques. The GLC synthesized at optimized conditions shows interlaced structure with an average thickness of 3 nm. Platinum on GLC electrocatalysts were prepared for methanol oxidation in acidic media for the first time. They show extremely higher activity for methanol oxidation compared to Pt/C electrocatalyst for the same Pt loadings. GLCs act as structural units to form mesopores and channels in the catalyst layers, which lead to the increase of the electrochemical active surface area and improvement in the mass transport by reducing the liquid sealing effect. © 2008 Elsevier Ltd. All rights reserved.
Original languageEnglish
Pages (from-to)531-536
JournalCarbon
Volume46
Issue number3
DOIs
Publication statusPublished - Mar 2008
Externally publishedYes

Bibliographical note

Publication details (e.g. title, author(s), publication statuses and dates) are captured on an “AS IS” and “AS AVAILABLE” basis at the time of record harvesting from the data source. Suggestions for further amendments or supplementary information can be sent to [email protected].

Funding

This work was financially supported by the Natural Science Foundation of Guangdong Province of China (04300695) and the Natural Science Foundation of China (U0734005, 20476108 and 20676049). Funding by the academic research fund AcRF tier 1 (RG40/05) and AcRF tier 2 (ARC11/06) of the Ministry of Education (Singapore) are also greatly acknowledged.

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