Figure1. Schematic illustration of the most favorable CO2 hydrogenation pathways on different cubic (c–In₂O₃) and hexagonal indium oxide (c–In₂O₃) surfaces [Figures adapted from Science Advances]

Catalytic hydrogenation of carbon dioxide (CO₂) is a green and sustainable means of synthesizing commodity chemicals such as methanol. This conversion process is key to realizing the “methanol economy” or creating “liquid sunshine,” both aspects of the circular economy. Recent studies revealed the potential for a family of metal oxides to catalyze this reaction. However, further optimizing their catalytic performance for industrial applications remained a great challenge, mostly due to the difficulties related to the need for rational design and controlled synthesis.

A team jointly led by Professors. Sun Yuhan, Gao Peng, and Li Shenggang at the Shanghai Advanced Research Institute (SARI) of the Chinese Academy of Sciences took up that challenge, and have reported a successful case of theory-guided rational design of indium oxide (In₂O₃) catalysts for CO₂ hydrogenation to methanol with high activity and selectivity. The new findings were published in the latest issue of Science Advances on June 17.

To rationally design In₂O₃-based nanocatalysts with favorable methanol synthesis performance, researchers carried out extensive density functional theory (DFT) calculations to establish the catalytic mechanism of the In₂O₃ catalyst during CO₂ hydrogenation to methanol and carbon dioxide by identifying preferred pathways. The computational modeling identified the rarely studied {104} facet of hexagonal In₂O₃ as the most favorable for methanol synthesis.

On the basis of this theoretical prediction, several experimental methods were then employed to synthesize In₂O₃ catalysts in different phases with distinct morphologies.

Interestingly, one of the four In₂O₃ catalysts synthesized in this way was confirmed to mainly expose the theoretically identified {104} facets. This catalyst also exhibited the best performance in terms of both activity and selectivity, confirming the DFT prediction. The methanol synthesis reaction catalyzed by this catalyst is favorable even at the very high temperature of 360 °C.

The space-time yield of methanol reached 10.9 mmol/g/hour at this temperature, which surpassed that of all previously known catalysts for this reaction, including previously reported In₂O₃-based catalysts and well-known Cu-based catalysts.

The In₂O₃ catalyst discovered in this research is promising as a way of directly converting CO₂ into methanol for industrial applications. In addition, the discovery of this In₂O₃ catalyst will promote the further development of oxide/zeolite bifunctional catalysts for direct CO₂ hydrogenation to various C₂₊ hydrocarbons (lower olefins, gasoline, aromatics and so on) via the methanol intermediate. Just as importantly, this discovery also highlights the pivotal role of computational science in helping to design industrially relevant catalysts. 

For more information, please contact:

Prof. Sun Yuhan

Email: sunyh@sari.ac.cn

Shanghai Advanced Research Institute, Chinese Academy of Sciences

Source: Shanghai Advanced Research Institute,

Chinese Academy of Sciences