Reversible adapting layer produces robust single-crystal electrocatalyst for oxygen evolution

Electrochemically converting water into oxygen/hydrogen gas is ideal for high-density renewable energy storage in which robust electrocatalysts for efficient oxygen evolution play crucial roles. To date, however, electrocatalysts with long-term stability have remained elusive. Here we report that si...

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Veröffentlicht in:Nature communications 2015-08, Vol.6 (1), p.8106-8106, Article 8106
Hauptverfasser: Tung, Ching-Wei, Hsu, Ying-Ya, Shen, Yen-Ping, Zheng, Yixin, Chan, Ting-Shan, Sheu, Hwo-Shuenn, Cheng, Yuan-Chung, Chen, Hao Ming
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Sprache:eng
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Zusammenfassung:Electrochemically converting water into oxygen/hydrogen gas is ideal for high-density renewable energy storage in which robust electrocatalysts for efficient oxygen evolution play crucial roles. To date, however, electrocatalysts with long-term stability have remained elusive. Here we report that single-crystal Co 3 O 4 nanocube underlay with a thin CoO layer results in a high-performance and high-stability electrocatalyst in oxygen evolution reaction. An in situ X-ray diffraction method is developed to observe a strong correlation between the initialization of the oxygen evolution and the formation of active metal oxyhydroxide phase. The lattice of skin layer adapts to the structure of the active phase, which enables a reversible facile structural change that facilitates the chemical reactions without breaking the scaffold of the electrocatalysts. The single-crystal nanocube electrode exhibits stable, continuous oxygen evolution for >1,000 h. This robust stability is attributed to the complementary nature of defect-free single-crystal electrocatalyst and the reversible adapting layer. There is extensive research into water-oxidation electrocatalysts which exhibit long-term stability. Here, the authors report a single-crystal cobalt oxide electrocatalyst displaying high activity and stability, and develop an in situ X-ray diffraction method to probe the structure–activity relationship.
ISSN:2041-1723
2041-1723
DOI:10.1038/ncomms9106