Abstract
One of novel porous 1-D architectures, mesopore-functional carbon sphere nanochains (MCSNs), with highly interrelated networks have been directly evolved from the colloidal carbon sphere nanochains (CCSNs) through a unique Li2CO3-molten salt strategy. The PtRu/MCSNs hybrid system, achieved by rational integration of 2.5-nm-size PtRu alloy NPs into the mesopores of MCSNs were prepared, and for comparison, the solid carbon sphere nanochain (SCSN)-supported PtRu NPs (PtRu/SCSN) and benchmark carbon (Vulcan XC-72)-supported PtRu (PtRu/C) were also prepared. It is demonstrated that the PtRu/MCSN hybrid system exhibited superior catalytic properties toward methanol oxidation with specially enhanced catalytic activity and desirable stability. The forward peak current density of PtRu/MCSNs (437mAmg−1) was obviously much higher than those of PtRu/SCSNs (265mAmg−1) and PtRu/C (310mAmg−1). The onset potential of PtRu/MCSNs (0.24V) is much earlier than those of PtRu/SCSNs (0.38V) and PtRu/C (0.37V). This attractive efficiency can be ascribed to the functionalities of mesoporous carbon support, which affords more efficient electron transfer and better mass transport, maximizing the availability of nano PtRu catalysts.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Similar Papers
More From: Electrochimica Acta
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.