4.8 Article

Trace doping of early transition metal enabled efficient and durable oxygen reduction catalysis on Pt-based ultrathin nanowires

期刊

APPLIED CATALYSIS B-ENVIRONMENTAL
卷 303, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.apcatb.2021.120918

关键词

Ultrathin Re-PtNiGa nanowires; Doping of early transition metal; Multicomponent alloy; Electrocatalyst; Oxygen reduction reaction

资金

  1. National Natural Science Foundation of China [U2032149, 21905089, 22102052, 51876173]
  2. Hunan Provincial Natural Science Foundation of China [2020JJ2001, 2020JJ5041, 2020JJ5043]
  3. Hefei National Laboratory for Physical Sciences at the Microscale [KF2020108]
  4. Hunan Provincial Graduate Research Innovation [CX20200452]
  5. Fundamental Research Funds for the Central Universities
  6. Australian Government
  7. Australian Research Council [LE190100021]

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The study introduces early transition metal Re into ultrathin PtNiGa nanowires for the first time, showcasing significant enhancements in activity and durability. Experiment results demonstrate that Re-PtNiGa tetrametallic nanowires exhibit superior performance in terms of mass activity and durability.
Discovering an active and durable catalyst for oxygen reduction reaction is crucial to the commercialization of fuel cells, but remains grand challenging. Here we report, for the first time, the trace doping of early transition metal (ETM) Re into ultrathin PtNiGa nanowires (Re-PtNiGa NWs) to construct a novel catalyst integrating the superior activity, long-time durability, and high utilization efficiency of Pt atoms. Impressively, the Re-PtNiGa tetrametallic NWs present a 19.6-fold enhancement in mass activity (3.49 A mg(Pt)(-1)) compared to commercial Pt/C catalyst and only a 10.6% loss in mass activity after 20,000 cycles of durability test. Moreover, the real fuel cell assembled by Re-PtNiGa NWs on the cathode strongly supports its great potential in fuel cells. The density functional theory calculations reveal that introduction of ETM Re into PtNiGa NWs could weaken binding strength of oxygenated species and elevate dissolution potential, well rationalizing the great enhancements in activity and durability.

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