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The widespread commercial application of direct formate fuel cell (DFFC) is limited by the lack of efficient electrocatalysts for the formate oxidation reaction (FOR). AgPdCo hollow nanospheres (H-NSs) with jagged surfaces are successfully synthesized via a facile method involving the wet-chemical synthesis of AgPdCo nanospheres (NSs) and galvanic replacement reaction between Pd salt and AgPdCo NSs. Surpassing Ag30Pd69Co1 NSs and most of previously reported electrocatalysts, Ag9Pd90Co1 H-NSs exhibit extremely high FOR activity with a peak current density of 3.08 A·mgPd-1. Apart from the competitive activity, Ag9Pd90Co1 H-NSs show greatly improved chronoamperometric and cycling stability, whereby the current density retains about 0.24 A·mgPd-1 after 3,600 s electrocatalysis and the mass activity maintains 54.06% of the initial value after 500 cycles. The unique hollow nanosphere and synergistic effect are responsible for the enhanced activity and stability. This study will provide new clues for the development of outstanding electrocatalysts.

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Publication history
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Acknowledgements

Publication history

Received: 22 August 2020
Revised: 15 October 2020
Accepted: 01 November 2020
Published: 05 July 2021
Issue date: July 2021

Copyright

© Tsinghua University Press and Springer-Verlag GmbH Germany, part of Springer Nature 2020

Acknowledgements

This work was supported by the National Natural Science Foundation of China (Nos. 51874243, 51271148, and 50971100), the Research Fund of State Key Laboratory of Solidification Processing (NPU), China (No. 2020-TS-02), the Project of Transformation of Scientific and Technological Achievements of NWPU (No. 19-2017), and the Open Fund of State Key Laboratory of Advanced Technology for Material Synthesis and Processing (Wuhan University of Technology, No. 2018-KF-18). We would like to thank the Analytical & Testing Center of Northwestern Polytechnical University for TEM and XPS characterizations.

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