Lattice Mismatched Platinum-Tellurium@Platinum-Ruthenium Core@Shell Nanorods Achieve Ultrahigh Alkaline Hydrogen Electrocatalysis for Dual Practical Devices.
basic_science · Level V
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- Record sourced from PubMed, PMID 41420356.
- Also identified by DOI 10.1002/adma.202517683.
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Abstract
Lattice mismatch engineering is necessary yet challenging for core@shell structured platinum (Pt)-based catalysts in alkaline hydrogen electrocatalysis. Herein, a series of lattice mismatched Pt-tellurium@Pt-ruthenium core@shell nanorods (LM-PtTe<sub>2</sub>@Pt<sub>x</sub>Ru NRs, x = 2, 4, 9, 12, 16) are constructed for alkaline hydrogen oxidation reaction (HOR) and hydrogen evolution reaction (HER). The optimized LM-PtTe<sub>2</sub>@Pt<sub>9</sub>Ru/C exhibits much better HOR and HER performances versus commercial PtRu/C and Pt/C. More importantly, its ultrahigh membrane electrode assembly (MEA) power densities of 26.4/21.0 W mg<sub>Pt+Ru</sub> <sup>-1</sup> in H<sub>2</sub>-O<sub>2</sub>/H<sub>2</sub>-air media for anion exchange membrane fuel cell (AEMFC) and remarkable MEA performance of 1.55 V@0.5 A cm<sup>-2</sup>/2.0 V@5.8 A cm<sup>-2</sup> for AEM water electrolysis (AEMWE) outperform the vast majority of PtRu-based catalysts reported to date, displaying an unprecedented potential in dual practical devices. The lattice mismatch degree of 18.7% between trigonal PtTe<sub>2</sub> and cubic Pt<sub>9</sub>Ru induces numerous lattice dislocations and unusual lattice strain effect in LM-PtTe<sub>2</sub>@Pt<sub>9</sub>Ru/C, which simultaneously optimizes the surface electron distribution and the adsorption of intermediates, responsible for its high hydrogen catalysis performance. This work aims to achieve the high-performance MEA catalysis for AEMFC and AEMWE with lattice mismatch engineering induced by these well-organized PtRu-based core@shell nanocatalysts.