Hexagonal prism-shaped CuO/SnO <sub>2</sub> heterostructure for high-performance CO <sub>2</sub> ER to formate

A hexagonal prism-shaped CuO/SnO<sub>2</sub> heterostructured catalyst with electron-enriched SnO<sub>2</sub> active sites was designed and synthesized. The formation of the CuO/SnO<sub>2</sub> heterointerface and electron-enriched SnO<sub>2</sub> active sites significantly enhanced the catalytic activity and selectivity for HCOO<sup>-</sup> in electrochemical reduction of carbon dioxide (CO<sub>2</sub>ER), while the well-defined hexagonal prismatic architecture provided catalytic and morphological stability. Consequently, the catalyst delivered a <i>j</i><sub>HCOO<sup>-</sup></sub> surpassing that of pure SnO<sub>2</sub> by 5 mA cm<sup>-2</sup> at -1.2 V <i>vs.</i> RHE and achieved FE<sub>HCOO<sup>-</sup></sub> up to 97% at -0.9 V <i>vs.</i> RHE, retaining FE<sub>HCOO<sup>-</sup></sub> above 80% with negligible current density decay after 36 hours of durability testing.

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Publication Details

Journal
Chemical Communications
Published
2025-01-01
DOI
https://doi.org/10.1039/d5cc02980e
Primary Topic
CO2 Reduction Techniques and Catalysts
Type
article
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article

Hexagonal prism-shaped CuO/SnO 2 heterostructure for high-performance CO 2 ER to formate

Xi Hu, Zidong Wei, Jingru Zhang, Xuejie Liu et al.
Chemical Communications
CO2 Reduction Techniques and Catalysts
article

Hexagonal prism-shaped CuO/SnO 2 heterostructure for high-performance CO 2 ER to formate

Xi Hu, Zidong Wei, Jingru Zhang, Xuejie Liu, Yanqiu Du, Zhiyong Yan
article en

Abstract

A hexagonal prism-shaped CuO/SnO<sub>2</sub> heterostructured catalyst with electron-enriched SnO<sub>2</sub> active sites was designed and synthesized. The formation of the CuO/SnO<sub>2</sub> heterointerface and electron-enriched SnO<sub>2</sub> active sites significantly enhanced the catalytic activity and selectivity for HCOO<sup>-</sup> in electrochemical reduction of carbon dioxide (CO<sub>2</sub>ER), while the well-defined hexagonal prismatic architecture provided catalytic and morphological stability. Consequently, the catalyst delivered a <i>j</i><sub>HCOO<sup>-</sup></sub> surpassing that of pure SnO<sub>2</sub> by 5 mA cm<sup>-2</sup> at -1.2 V <i>vs.</i> RHE and achieved FE<sub>HCOO<sup>-</sup></sub> up to 97% at -0.9 V <i>vs.</i> RHE, retaining FE<sub>HCOO<sup>-</sup></sub> above 80% with negligible current density decay after 36 hours of durability testing.

Chemical CommunicationsVol. 61(79)
Chongqing University (CN), Jiaxing University (CN)
Openalex Percentile: Top 85%
CO2 Reduction Techniques and Catalysts
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