Inverse In2O3-x/Ni interfaces via Ni3InC0.5 surface reconstruction for efficient CO2 hydrogenation to methanol

Catalyst surface reconstruction under reaction conditions is ubiquitous and crucial for creating unusual active sites, thereby enhancing catalytic performance. Here, we report the surface reconstruction of supported Ni<sub>3</sub>InC<sub>0.5</sub> nanoparticles, leading to the formation of defective In<sub>2</sub>O<sub>3-x</sub> overlayers and inverse In<sub>2</sub>O<sub>3-x</sub>/Ni interfaces, driven by CO<sub>2</sub>-induced selective surface oxidation during CO<sub>2</sub> hydrogenation. The synergy between In<sub>2</sub>O<sub>3-x</sub> overlayers and inverse In<sub>2</sub>O<sub>3-x</sub>/Ni interfaces facilitates CO<sub>2</sub> adsorption and activation, as well as the following hydrogenation of HCOO<sup>*</sup> and CH<sub>x</sub>O<sup>*</sup> intermediates, enabling efficient methanol synthesis from CO<sub>2</sub>. Accordingly, the optimized LDH-NiInCAl catalyst achieves an impressive CO<sub>2</sub> conversion of 19% with 65% methanol selectivity and 508.4 <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:mi>mg</mml:mi> <mml:msubsup><mml:mrow><mml:mi>g</mml:mi></mml:mrow> <mml:mrow><mml:mi>cat</mml:mi></mml:mrow> <mml:mrow><mml:mo>-</mml:mo> <mml:mn>1</mml:mn></mml:mrow> </mml:msubsup> <mml:msup><mml:mrow><mml:mi>h</mml:mi></mml:mrow> <mml:mrow><mml:mo>-</mml:mo> <mml:mn>1</mml:mn></mml:mrow> </mml:msup> </mml:math> methanol space-time yield at 260 °C, 5 MPa, and 12000 <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:mi>mL</mml:mi> <mml:msubsup><mml:mrow><mml:mi>g</mml:mi></mml:mrow> <mml:mrow><mml:mi>cat</mml:mi></mml:mrow> <mml:mrow><mml:mo>-</mml:mo> <mml:mn>1</mml:mn></mml:mrow> </mml:msubsup> <mml:msup><mml:mrow><mml:mi>h</mml:mi></mml:mrow> <mml:mrow><mml:mo>-</mml:mo> <mml:mn>1</mml:mn></mml:mrow> </mml:msup> </mml:math> , outperforming commercial Cu/ZnO/Al<sub>2</sub>O<sub>3</sub> catalysts. This work showcases how structural evolution and surface reconstruction enhance catalytic performance, providing new insights into the dynamic structure-activity relationship.

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Journal
Nature Communications
Published
2025-12-08
DOI
https://doi.org/10.1038/s41467-025-65929-z
Citations
6
Primary Topic
Catalysts for Methane Reforming
Type
article
Field-Weighted Citation Impact
2.33

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article

Inverse In2O3-x/Ni interfaces via Ni3InC0.5 surface reconstruction for efficient CO2 hydrogenation to methanol

Jiyi Chen, Shixiong Tang, Wenyan Jia, Maoshuai Li et al.
6 citations
Nature Communications
Catalysts for Methane Reforming
2.33
article

Inverse In2O3-x/Ni interfaces via Ni3InC0.5 surface reconstruction for efficient CO2 hydrogenation to methanol

Jiyi Chen, Shixiong Tang, Wenyan Jia, Maoshuai Li, Kang Hui Lim, Shibo Xi, Mingwu Tan, Jing Lv, Yong Wang, Bingqing Yao, Zhenmei Zhang, Qian He, Ziwen Hao, Yue Wang, Xiaohui Zi, Sibudjing Kawi, Heng Zhang, Xinbin Ma, Xiaoyu Han, Qi Yang, Tian‐Tian Xiao
article en
6 citations

Abstract

Catalyst surface reconstruction under reaction conditions is ubiquitous and crucial for creating unusual active sites, thereby enhancing catalytic performance. Here, we report the surface reconstruction of supported Ni<sub>3</sub>InC<sub>0.5</sub> nanoparticles, leading to the formation of defective In<sub>2</sub>O<sub>3-x</sub> overlayers and inverse In<sub>2</sub>O<sub>3-x</sub>/Ni interfaces, driven by CO<sub>2</sub>-induced selective surface oxidation during CO<sub>2</sub> hydrogenation. The synergy between In<sub>2</sub>O<sub>3-x</sub> overlayers and inverse In<sub>2</sub>O<sub>3-x</sub>/Ni interfaces facilitates CO<sub>2</sub> adsorption and activation, as well as the following hydrogenation of HCOO<sup>*</sup> and CH<sub>x</sub>O<sup>*</sup> intermediates, enabling efficient methanol synthesis from CO<sub>2</sub>. Accordingly, the optimized LDH-NiInCAl catalyst achieves an impressive CO<sub>2</sub> conversion of 19% with 65% methanol selectivity and 508.4 <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:mi>mg</mml:mi> <mml:msubsup><mml:mrow><mml:mi>g</mml:mi></mml:mrow> <mml:mrow><mml:mi>cat</mml:mi></mml:mrow> <mml:mrow><mml:mo>-</mml:mo> <mml:mn>1</mml:mn></mml:mrow> </mml:msubsup> <mml:msup><mml:mrow><mml:mi>h</mml:mi></mml:mrow> <mml:mrow><mml:mo>-</mml:mo> <mml:mn>1</mml:mn></mml:mrow> </mml:msup> </mml:math> methanol space-time yield at 260 °C, 5 MPa, and 12000 <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:mi>mL</mml:mi> <mml:msubsup><mml:mrow><mml:mi>g</mml:mi></mml:mrow> <mml:mrow><mml:mi>cat</mml:mi></mml:mrow> <mml:mrow><mml:mo>-</mml:mo> <mml:mn>1</mml:mn></mml:mrow> </mml:msubsup> <mml:msup><mml:mrow><mml:mi>h</mml:mi></mml:mrow> <mml:mrow><mml:mo>-</mml:mo> <mml:mn>1</mml:mn></mml:mrow> </mml:msup> </mml:math> , outperforming commercial Cu/ZnO/Al<sub>2</sub>O<sub>3</sub> catalysts. This work showcases how structural evolution and surface reconstruction enhance catalytic performance, providing new insights into the dynamic structure-activity relationship.

Nature CommunicationsVol. 16(1)
Agency for Science, Technology and Research (SG), Tianjin University (CN), National University of Singapore (SG), Collaborative Innovation Center of Chemical Science and Engineering Tianjin (CN), State Key Laboratory of Chemical Engineering (CN), Tianjin haihe hospital (CN), Xinjiang University (CN)
National Research Foundation, Agency for Science, Technology and Research, National University of Singapore, National Research Foundation Singapore, National Natural Science Foundation of China, Tianjin University, National Key Research and Development Program of China
Openalex Percentile: Top 11%
Catalysts for Methane Reforming
2.33
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