期刊
CARBON
卷 49, 期 5, 页码 1699-1709出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.carbon.2010.12.055
关键词
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资金
- National Natural Science Foundation of China [50872124, 51003096]
- Zhejiang Provincial Natural Science Foundation of China [Y4100094]
- Science Foundation of Zhejiang Sci-Tech University (ZSTU) [1001803-Y]
- Research Fund for the Doctoral Program of Higher Education [20093318120003]
A nanomaterial-based metallophthalocyanine catalyst (CoTAPc-MWCNTs) was prepared by covalently immobilizing cobalt tetraaminophthalocyanine (CoTAPc) on multiwalled carbon nanotubes (MWCNTs). The decomposition reaction of H(2)O(2) was chosen to investigate the coupled catalytic performance. The results of electron paramagnetic resonance and online electrochemical experiments indicated that the catalytic mechanism of CoTAPc-MWCNTs is different from that of cobalt phthalocyanine molecular catalysts. The catalytic pathway of CoTAPc-MWCNTs involves the following steps: first, electron transfer from CoTAPc to H(2)O(2) occurs through the coordination between the central cobalt ion and H(2)O(2), reducing H(2)O(2) to H(2)O; second, electrons are transferred from MWCNTs to the oxidized CoTAPc, forming hole-doped MWCNTs; finally, hole-doped MWCNTs accept electrons from H(2)O(2), oxidizing H(2)O(2) to O(2). When using N,N-diethyl-1,4-phenylenediamine as a chromogenic substance, one obtained a quantitative estimate of holes injected in MWCNTs, corresponding to 1 hole for about 55 carbon atoms. Furthermore, CoTAPc-MWCNTs exhibit very unusual characteristics of controlled catalysis due to the special hydrophobic surface of the MWCNTs, and can be used as an interfacial catalyst for the determination of H(2)O(2) concentration. (C) 2010 Elsevier Ltd. All rights reserved.
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