In situ synthesis of palladium nanoparticles on multi-walled carbon nanotubes and their electroactivity for ethanol oxidation

Pd nanoparticles (Pd-NPs) were prepared and directly anchored on the surface of multi-walled carbon nanotubes (MWCNTs) in the absence of chemical reduction agent, where MWCNTs were used as both the chemical reduction agent and the support substrate of Pd-NPs. Effect of various surfactants on the in...

Full description

Saved in:
Bibliographic Details
Published inRare metals Vol. 32; no. 6; pp. 586 - 591
Main Authors Yi, Qing-Feng, Sun, Li-Zhi
Format Journal Article
LanguageEnglish
Published Berlin/Heidelberg Springer Berlin Heidelberg 01.12.2013
Springer Nature B.V
School of Chemistry and Chemical Engineering, Hunan University of Science and Technology, Xiangtan 411201, China
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Pd nanoparticles (Pd-NPs) were prepared and directly anchored on the surface of multi-walled carbon nanotubes (MWCNTs) in the absence of chemical reduction agent, where MWCNTs were used as both the chemical reduction agent and the support substrate of Pd-NPs. Effect of various surfactants on the in situ deposition of Pd-NPs on MWCNTs was investigated. When MWCNTs were modified with a cationic surfactant (hexadecyl trimethyl ammonium bromide, CTAB), the amount of the Pd-NPs (Pd-NP/CTAB-MWCNT) generated by such an in situ deposition method gets a notable increase, and the size of the as-synthesized Pd-NPs becomes smaller, compared with those in the absence of any surfactant (Pd-NP/MWCNT) or in the presence of an anionic surfactant SDS (Pd-NP/SDS-MWCNT) and a neutral surfactant OP (Pd-NP/OP-MWCNT). Results show that the MWCNTs modified with CTAB are propitious to the in situ reduction of Pd 2+ . Among the prepared catalysts, Pd-NP/CTAB-MWCNT displays the highest electroactivity for ethanol oxidation in alkaline media.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:1001-0521
1867-7185
DOI:10.1007/s12598-013-0179-x