Synthesis of defect-rich La <sub>2</sub> O <sub>2</sub> CO <sub>3</sub> supports for enhanced CO <sub>2</sub> -to-methanol conversion efficiency

Converting CO 2 to methanol is crucial for addressing fuel scarcity and mitigating the greenhouse effect. Cu-based catalysts, with their diverse surface states, offer the potential to control reaction pathways and generate reactive H* species. However, a major challenge lies in oxidizing active Cu 0 species by water generated during the catalytic process. While nonreducible metal oxides are beneficial in stabilizing metallic states, their limited capability to generate surface oxygen vacancies (O V ) hinders CO 2 activation. Herein, we present a strategy by doping Nd into a La 2 O 2 CO 3 (LOC) support, enhancing O V formation by disrupting its lattice dyadicity. This leads to higher Cu 0 concentration and improved CO 2 activation. The resulting Cu/LOC:Nd catalyst notably outperforms Cu/LOC and CuZnAl catalysts, achieving a methanol yield of 9.9 moles of methanol per hour per mole of Cu. Our approach opens up possibilities for enhancing Cu-based catalysts in CO 2 conversion.

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Publication Details

Journal
Science Advances
Published
2024-12-04
DOI
https://doi.org/10.1126/sciadv.adr3332
Citations
22
Primary Topic
Catalytic Processes in Materials Science
Type
article
Field-Weighted Citation Impact
2.58

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article

Synthesis of defect-rich La 2 O 2 CO 3 supports for enhanced CO 2 -to-methanol conversion efficiency

Shuyan Song, Weidong Shi, Xiao Wang, Rui Zhang et al.
22 citations
Science Advances
Catalytic Processes in Materials Science
2.58
article

Synthesis of defect-rich La 2 O 2 CO 3 supports for enhanced CO 2 -to-methanol conversion efficiency

Shuyan Song, Weidong Shi, Xiao Wang, Rui Zhang, Hongjie Zhang, Xudong Sun, Huilin Wang, Ke Wang
article en
22 citations

Abstract

Converting CO 2 to methanol is crucial for addressing fuel scarcity and mitigating the greenhouse effect. Cu-based catalysts, with their diverse surface states, offer the potential to control reaction pathways and generate reactive H* species. However, a major challenge lies in oxidizing active Cu 0 species by water generated during the catalytic process. While nonreducible metal oxides are beneficial in stabilizing metallic states, their limited capability to generate surface oxygen vacancies (O V ) hinders CO 2 activation. Herein, we present a strategy by doping Nd into a La 2 O 2 CO 3 (LOC) support, enhancing O V formation by disrupting its lattice dyadicity. This leads to higher Cu 0 concentration and improved CO 2 activation. The resulting Cu/LOC:Nd catalyst notably outperforms Cu/LOC and CuZnAl catalysts, achieving a methanol yield of 9.9 moles of methanol per hour per mole of Cu. Our approach opens up possibilities for enhancing Cu-based catalysts in CO 2 conversion.

Science AdvancesVol. 10(49)
Jiangsu University (CN), University of Science and Technology of China (CN), Chinese Academy of Sciences (CN), Changchun Institute of Applied Chemistry (CN), Tsinghua University (CN)
Salt Science Research Foundation, People's Government of Jilin Province, National Science and Technology Major Project
Openalex Percentile: Top 6%
Catalytic Processes in Materials Science
2.58
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