Loading…
Green preparation of self-supporting platinum nanoflower catalyst and its electrocatalytic oxidation performance of methanol
[Display omitted] •NaOH-KOH low temperature molten salt was used as flux for preparing Pt nanoflower catalyst.•The catalyst has 3D self-supporting framework and clean surface with lots of active sites.•The product can be directly used for electrochemical catalysis without any pretreatment.•The Pt na...
Saved in:
Published in: | Carbon resources conversion 2023-09, Vol.6 (3), p.167-172 |
---|---|
Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | [Display omitted]
•NaOH-KOH low temperature molten salt was used as flux for preparing Pt nanoflower catalyst.•The catalyst has 3D self-supporting framework and clean surface with lots of active sites.•The product can be directly used for electrochemical catalysis without any pretreatment.•The Pt nanoflower catalyst exhibited excellent performance in MOR.
The three-dimensional (3D) self-supporting Pt nanoflower catalyst was prepared by using Pt organic compounds as precursors in a low-temperature molten salt system. The obtained Pt nanoflower nanoparticle can reach 400–500 nm with a face-centered cubic structure, which has the structural characteristics of a loose framework and more exposed active sites. The surfactant-free Pt nanoflower was directly used as methanol electrooxidation reaction (MOR) electrocatalysts without any pretreatment and activated carbon support. The results of electrochemical catalytic oxidation of methanol showed that the Pt nanoflower catalyst exhibit more enhanced electrocatalytic oxidation performance toward methanol compared with the commercial platinum black catalyst. The green and effective method can be developed and expected to enable mass production of fuel cell catalysts. |
---|---|
ISSN: | 2588-9133 2588-9133 |
DOI: | 10.1016/j.crcon.2023.01.002 |