News Release

100% CO2 to Ch4 conversion achieved with non-precious Co@ZnO catalyst in hot water

Peer-Reviewed Publication

Shanghai Jiao Tong University Journal Center

100% Conversion of CO2–CH4 with Non-Precious Co@ZnO Catalyst in Hot Water

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  • The combination of solar energy and underground hydrothermal environment supports the sustained and efficient CH4 production from CO2.
  • Nanosheets of honeycomb ZnO were formed in-situ on the Co surface, resulting in a new motif (Co@ZnO catalyst) that inhibits Co deactivation through ZnO-assisted CoOx reduction.
  • The stabilized Co and interaction between Co and ZnO inhibited unwanted side reaction pathways via CO production, ensuring formic acid formed as an intermediate, leading to 100% CH4 yield.
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Credit: Yang Yang, Xu Liu, Daoping He, Fangming Ji.

The efficient conversion of carbon dioxide (CO2) into valuable hydrocarbons is a critical step towards sustainable energy solutions. Now, researchers from the School of Environmental Science and Engineering at Shanghai Jiao Tong University, led by Professor Daoping He and Professor Fangming Jin, have developed a novel hydrothermal CO2 methanation process using a non-precious Co@ZnO catalyst. This innovative approach achieves a remarkable 100% conversion of CO2 to methane (CH4) under optimized conditions, offering a sustainable and efficient solution for CO2 utilization.

Why This Research Matters

  • High Efficiency: The Co@ZnO catalyst enables a complete conversion of CO2 to CH4, with no detectable by-products such as CO or higher hydrocarbons.
  • Non-Precious Metals: The use of cobalt (Co) and zinc (Zn) as catalyst components avoids the need for expensive noble metals, making the process more cost-effective.
  • Sustainable Energy: This method leverages solar energy and hydrothermal conditions, providing a green pathway for CO2 reduction and methane production.

Innovative Design and Features

  • Co@ZnO Catalyst: The catalyst features a unique structure where honeycomb-like ZnO nanosheets grow in situ on the Co surface. This structure stabilizes Co in its metallic state and enhances its catalytic activity.
  • Hydrothermal Process: The reaction is conducted in a hydrothermal environment, where Zn is oxidized to produce hydrogen, which then reduces CO2 to formic acid and ultimately to CH4.
  • Stable and Selective: The Co@ZnO catalyst maintains its activity over multiple cycles, with no significant leaching of Co, ensuring long-term stability and high selectivity for CH4 production.

Experimental and Practical Validation

  • Reaction Mechanism: In situ hydrothermal Fourier Transform Infrared (FTIR) spectroscopy confirms that formic acid is an intermediate in the CO2 methanation process. The Co@ZnO catalyst effectively converts formic acid to CH4 without forming CO.
  • Optimization: The study identifies optimal conditions for maximum CH4 yield, including reaction temperature, duration, and the ratio of Zn to Co.
  • Energy Efficiency: The process is energetically favorable, with the energy released from the reaction compensating for the energy input required to heat the reactants after just three moles of reaction.

Future Outlook

This groundbreaking work presents a simple, sustainable, and highly efficient approach for CO2 methanation. By using abundant and non-precious metals, this method offers significant potential for practical applications in CO2 utilization and sustainable energy production. Further research could explore the scalability and integration of this process with renewable energy systems.

Stay tuned for more innovative solutions from Professor Daoping He and Professor Fangming Jin at Shanghai Jiao Tong University!


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