z-logo
Premium
Three‐Dimensional Nitrogen‐Doped Reduced Graphene Oxide–Carbon Nanotubes Architecture Supporting Ultrafine Palladium Nanoparticles for Highly Efficient Methanol Electrooxidation
Author(s) -
Song Hejie,
Yang Liming,
Tang Yanhong,
Yan Dafeng,
Liu Chengbin,
Luo Shenglian
Publication year - 2015
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201502804
Subject(s) - graphene , materials science , carbon nanotube , chronoamperometry , electrocatalyst , raman spectroscopy , oxide , chemical engineering , cyclic voltammetry , nanoparticle , x ray photoelectron spectroscopy , catalysis , methanol , nanotechnology , inorganic chemistry , electrochemistry , chemistry , organic chemistry , electrode , optics , metallurgy , physics , engineering
A three‐dimensional (3D) nitrogen‐doped reduced graphene oxide (rGO)–carbon nanotubes (CNTs) architecture supporting ultrafine Pd nanoparticles is prepared and used as a highly efficient electrocatalyst. Graphene oxide (GO) is first used as a surfactant to disperse pristine CNTs for electrochemical preparation of 3D rGO@CNTs, and subsequently one‐step electrodeposition of the stable colloidal GO–CNTs solution containing Na 2 PdCl 4 affords rGO@CNTs‐supported Pd nanoparticles. Further thermal treatment of the Pd/rGO@CNTs hybrid with ammonia achieves not only in situ nitrogen‐doping of the rGO@CNTs support but also extraordinary size decrease of the Pd nanoparticles to below 2.0 nm. The resulting catalyst is characterized by scanning and transmission electron microscopy, X‐ray diffraction, Raman spectroscopy, and X‐ray photoelectron spectroscopy. Catalyst performance for the methanol oxidation reaction is tested through cyclic voltammetry and chronoamperometry techniques, which shows exceedingly high mass activity and superior durability.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here