A Janus Platinum/Tin Oxide Heterostructure for Durable Oxygen Reduction Reaction

Designing efficient and durable electrocatalysts for oxygen reduction reaction (ORR) is essential for proton exchange membrane fuel cells (PEMFCs). Platinum-based catalysts are considered efficient ORR catalysts due to their high activity. However, the degradation of Pt species leads to poor durability of catalysts, limiting their applications in PEMFCs. Herein, a Janus heterostructure is designed for high durability ORR in acidic media. The Janus heterostructure composes of crystalline platinum and cassiterite tin oxide nanoparticles with carbon support (J-Pt@SnO<sub>2</sub>/C). Based on the synchrotron fine structure analysis and electrochemical investigation, the crystalline reconstruction and charge redistribution at the interface of Janus structure are revealed. The tightly coupled interface could optimize the valance states of Pt and the adsorption/desorption of oxygenated intermediates. As a result, the J-Pt@SnO<sub>2</sub>/C catalyst possesses distinguishing long-term stability during the accelerated durability test without obvious degradation after 40 000 cycles and keeps the majority of activity after 70 000 cycles. Meanwhile, the catalyst exhibits outstanding activity with half-wave potential at 0.905 V and a mass activity of 0.355 A mg<sub>Pt</sub> <sup>-1</sup> (2.7 times higher than Pt/C). The approach of the Janus catalyst paves an avenue for designing highly efficient and stable Pt-based ORR catalyst in the future implementation.

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Publication Details

Journal
Small
Published
2024-10-02
DOI
https://doi.org/10.1002/smll.202405234
Citations
2
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
0.20

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article

A Janus Platinum/Tin Oxide Heterostructure for Durable Oxygen Reduction Reaction

Ruyang Wang, Boyan Zhang, Peiyu Ma, Jun Bao et al.
2 citations
Small
Electrocatalysts for Energy Conversion
0.20
article

A Janus Platinum/Tin Oxide Heterostructure for Durable Oxygen Reduction Reaction

Ruyang Wang, Boyan Zhang, Peiyu Ma, Jun Bao, Heng Cao
article en
2 citations

Abstract

Designing efficient and durable electrocatalysts for oxygen reduction reaction (ORR) is essential for proton exchange membrane fuel cells (PEMFCs). Platinum-based catalysts are considered efficient ORR catalysts due to their high activity. However, the degradation of Pt species leads to poor durability of catalysts, limiting their applications in PEMFCs. Herein, a Janus heterostructure is designed for high durability ORR in acidic media. The Janus heterostructure composes of crystalline platinum and cassiterite tin oxide nanoparticles with carbon support (J-Pt@SnO<sub>2</sub>/C). Based on the synchrotron fine structure analysis and electrochemical investigation, the crystalline reconstruction and charge redistribution at the interface of Janus structure are revealed. The tightly coupled interface could optimize the valance states of Pt and the adsorption/desorption of oxygenated intermediates. As a result, the J-Pt@SnO<sub>2</sub>/C catalyst possesses distinguishing long-term stability during the accelerated durability test without obvious degradation after 40 000 cycles and keeps the majority of activity after 70 000 cycles. Meanwhile, the catalyst exhibits outstanding activity with half-wave potential at 0.905 V and a mass activity of 0.355 A mg<sub>Pt</sub> <sup>-1</sup> (2.7 times higher than Pt/C). The approach of the Janus catalyst paves an avenue for designing highly efficient and stable Pt-based ORR catalyst in the future implementation.

SmallVol. 20(49)
University of Science and Technology of China (CN), National Synchrotron Radiation Laboratory (CN), Collaborative Innovation Center of Chemistry for Energy Materials (CN)
National Natural Science Foundation of China, China Postdoctoral Science Foundation, National Key Research and Development Program of China, Fundamental Research Funds for the Central Universities
Responsible consumption and production, Life in Land
Openalex Percentile: Top 58%
Electrocatalysts for Energy Conversion
0.20
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