Multifunctional Active‐Center‐Transferable Platinum/Lithium Cobalt Oxide Heterostructured Electrocatalysts towards Superior Water Splitting
Designing cost‐effective and efficient electrocatalysts plays a pivotal role in advancing the development of electrochemical water splitting for hydrogen generation. Herein, multifunctional active‐center‐transferable heterostructured electrocatalysts, platinum/lithium cobalt oxide (Pt/LiCoO2) compos...
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Veröffentlicht in: | Angewandte Chemie International Edition 2020-08, Vol.59 (34), p.14533-14540 |
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Sprache: | eng |
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Zusammenfassung: | Designing cost‐effective and efficient electrocatalysts plays a pivotal role in advancing the development of electrochemical water splitting for hydrogen generation. Herein, multifunctional active‐center‐transferable heterostructured electrocatalysts, platinum/lithium cobalt oxide (Pt/LiCoO2) composites with Pt nanoparticles (Pt NPs) anchored on LiCoO2 nanosheets, are designed towards highly efficient water splitting. In this electrocatalyst system, the active center can be alternatively switched between Pt species and LiCoO2 for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), respectively. Specifically, Pt species are the active centers and LiCoO2 acts as the co‐catalyst for HER, whereas the active center transfers to LiCoO2 and Pt turns into the co‐catalyst for OER. The unique architecture of Pt/LiCoO2 heterostructure provides abundant interfaces with favorable electronic structure and coordination environment towards optimal adsorption behavior of reaction intermediates. The 30 % Pt/LiCoO2 heterostructured electrocatalyst delivers low overpotentials of 61 and 285 mV to achieve 10 mA cm−2 for HER and OER in alkaline medium, respectively.
Center of attention: Multifunctional platinum/lithium cobalt oxide (Pt/LiCoO2) heterostructures are prepared that allow the active center to be switched between Pt species for the hydrogen evolution reaction (HER) and LiCoO2 species for the oxygen evolution reaction (OER). |
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ISSN: | 1433-7851 1521-3773 |
DOI: | 10.1002/anie.202005241 |