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The phase transformation of catalysts has been extensively observed in heterogeneous catalytic reactions that hinder the long cycling catalysis, and it remains a big challenge to precisely control the active phase during the complex conditions in electrochemical catalysis. Here, we theoretically predict that carbon-based support could achieve the phase engineering regulation of catalysts by suppressing specific phase transformation. Taken single-walled carbon nanotube (SWCNT) as typical support, combined with calculated E-pH (Pourbaix) diagram and advanced synchrotron-based characterizations technologies prove there are two different active phases source from cobalt selenide which demonstrate that the feasibility of using support effect regulating the potential advantageous catalysts. Moreover, it is worth noting that the phase engineering derived Co3O4-SWCNT exhibits a low overpotential of 201 mV for delivering the current density of 10 mA/cm2 in electrocatalytic oxygen evolution reaction (OER). Also, it reaches a record current density of 529 mA/cm2 at 1.63 V (vs. RHE) in the electrocatalytic urea oxidation reaction (UOR), overwhelming most previously reported catalysts.

Publication history
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Acknowledgements

Publication history

Received: 25 May 2021
Revised: 13 July 2021
Accepted: 19 July 2021
Published: 07 August 2021
Issue date: March 2022

Copyright

© Tsinghua University Press and Springer-Verlag GmbH Germany, part of Springer Nature 2021

Acknowledgements

Acknowledgements

This work was financially supported in part by the National Key R&D Program of China (Nos. 2020YFA0405800 and 2017YFA0303500), the National Natural Science Foundation of China (NSFC) (Nos. U1932201, U2032113, and 22075264), CAS Collaborative Innovation Program of Hefei Science Center (Nos. 2019HSC-CIP002 and 2020HSC-CIP002), USTC Research Funds of the Double First-Class Initiative (No. YD2310002003), Institute of Energy, Hefei Comprehensive Nation Science Center,University Synergy Innovation Program of Anhui Province (GXXT-2020-002), and CAS Iterdisciplinary Innovation Team. L.S. acknowledges the support from Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), Nankai University (111 project, B12015). We thank the Shanghai synchrotron Radiation Facility (BL14W1, SSRF), the Beijing Synchrotron Radiation Facility (1W1B, BSRF), the Hefei Synchrotron Radiation Facility (MCD-A, BL10B, and MCD-B Soochow Beamline for Energy Materials at NSRL), and the USTC Center for Micro and Nanoscale Research and Fabrication for their help in characterizations.

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