Layered Na2Ti3O7-supported Ru catalyst for ambient CO2 methanation

The methanation of CO<sub>2</sub> offers a practical solution for storing renewable energy and mitigating global climate risks. However, the primary challenge lies in achieving efficient CH<sub>4</sub> production at lower temperatures. Here, we report a layered Na<sub>2</sub>Ti<sub>3</sub>O<sub>7</sub>-supported Ru catalyst as a stabilizer of low-valence Ru that enables CO<sub>2</sub> activation at low temperatures. This catalyst leads to a CH<sub>4</sub> production rate of 33.6 and 139.1 mmol g<sub>cat</sub><sup>-1</sup> h<sup>-1</sup> at 140 and 180 °C, respectively, with a gas hourly space velocity of 24,000 mL g<sup>-1</sup> h<sup>-</sup><sup>1</sup> at ambient pressure (1 bar), significantly surpassing state-of-the-art catalysts performance. Moreover, the catalyst demonstrates robustness to on-off intermittency and 220-hour long-term stability tests, indicating its reliability under challenging conditions. The catalyst is also successfully synthesized at the gram scale and on a 3D-printed metal self-catalytic reactor by a facile ion-exchange method, confirming its excellent scalability. This study marks a significant step forward in the design of catalysts for the low temperature CO<sub>2</sub> hydrogenation.

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Publication Details

Journal
Nature Communications
Published
2025-04-02
DOI
https://doi.org/10.1038/s41467-025-57954-9
Citations
22
Primary Topic
Catalysts for Methane Reforming
Type
article
Field-Weighted Citation Impact
8.56

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article

Layered Na2Ti3O7-supported Ru catalyst for ambient CO2 methanation

Hiromi Yamashita, Takayoshi Nakano, Hyojin Kim, Kohsuke Mori et al.
22 citations
Nature Communications
Catalysts for Methane Reforming
8.56
article

Layered Na2Ti3O7-supported Ru catalyst for ambient CO2 methanation

Hiromi Yamashita, Takayoshi Nakano, Hyojin Kim, Kohsuke Mori, Satoshi Ichikawa
article en
22 citations

Abstract

The methanation of CO<sub>2</sub> offers a practical solution for storing renewable energy and mitigating global climate risks. However, the primary challenge lies in achieving efficient CH<sub>4</sub> production at lower temperatures. Here, we report a layered Na<sub>2</sub>Ti<sub>3</sub>O<sub>7</sub>-supported Ru catalyst as a stabilizer of low-valence Ru that enables CO<sub>2</sub> activation at low temperatures. This catalyst leads to a CH<sub>4</sub> production rate of 33.6 and 139.1 mmol g<sub>cat</sub><sup>-1</sup> h<sup>-1</sup> at 140 and 180 °C, respectively, with a gas hourly space velocity of 24,000 mL g<sup>-1</sup> h<sup>-</sup><sup>1</sup> at ambient pressure (1 bar), significantly surpassing state-of-the-art catalysts performance. Moreover, the catalyst demonstrates robustness to on-off intermittency and 220-hour long-term stability tests, indicating its reliability under challenging conditions. The catalyst is also successfully synthesized at the gram scale and on a 3D-printed metal self-catalytic reactor by a facile ion-exchange method, confirming its excellent scalability. This study marks a significant step forward in the design of catalysts for the low temperature CO<sub>2</sub> hydrogenation.

Nature CommunicationsVol. 16(1)
The University of Osaka (JP)
New Energy and Industrial Technology Development Organization, Japan Science and Technology Agency, Core Research for Evolutional Science and Technology
Climate action
Openalex Percentile: Top 2%
Catalysts for Methane Reforming
8.56
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