Finding out robust active and sustainable catalyst towards alcohol electro-oxidation reaction is major challenges for large-scale commercialization of direct alcohol fuel cells. Herein, a robust Pt nanowires (NWs)/TiWO electrocatalyst, as the coherency of using non-carbon catalyst support and controlling the morphology and structure of the Pt nanocatalyst, was fabricated via an effortless chemical reduction reaction approach at room temperature without using surfactant/stabilizers or template to assemble an anodic electrocatalyst towards methanol electro-oxidation reaction (MOR) and ethanol electro-oxidation reaction (EOR). These observational results demonstrated that the Pt NWs/TiWO electrocatalyst is an intriguing anodic electrocatalyst, which can alter the state-of-the-art Pt NPs/C catalyst. Compared with the conventional Pt NPs/C electrocatalyst, the Pt NWs/TiWO electrocatalyst exhibited the lower onset potential (~0.1 V for MOR and ~0.2 for EOR), higher mass activity (~355.29 mA/mg for MOR and ~325.01 mA/mg for EOR) and much greater durability. The outperformance of the Pt NWs/TiWO electrocatalyst is ascribable to the merits of the anisotropic one-dimensional Pt nanostructure and the mesoporous TiWO support along with the synergistic effects between the TiWO support and the Pt nanocatalyst. Furthermore, this approach may provide a promising catalytic platform for fuel cell technology and a variety of applications.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6794307 | PMC |
http://dx.doi.org/10.1038/s41598-019-51235-4 | DOI Listing |
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