CO <sub>2</sub> Fixation and Release Mediated by Carbonate-Based Coordination Polymers

We demonstrate the synthesis of 11 carbonate (CO<sub>3</sub><sup>2-</sup>)-based coordination polymers (CPs) from CO<sub>2</sub> and reveal the structure-property correlation of CO<sub>2</sub> release upon decarbonation. The decarbonation temperatures (<i>T</i><sub>CO2</sub>) are tunable as factors of the electronegativity of metal ions and the coordination numbers of CO<sub>3</sub><sup>2-</sup> within the CP lattices. The structural tunability of CO<sub>3</sub><sup>2-</sup>-based CPs enables high gravimetric CO<sub>2</sub> contents (25-30 wt %) and <i>T</i><sub>CO2</sub> in the low-temperature range where low-grade waste heat can be utilized (170-230 °C). The decarbonation mechanism of CO<sub>3</sub><sup>2-</sup>-based CPs, which produces a discrete metal complex, is revealed by 3D electron diffraction and variable-temperature synchrotron X-ray diffraction.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-08-11
DOI
https://doi.org/10.1021/jacs.5c07425
Citations
1
Primary Topic
Carbon dioxide utilization in catalysis
Type
article
Field-Weighted Citation Impact
0.70

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article

CO 2 Fixation and Release Mediated by Carbonate-Based Coordination Polymers

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1 citations
Journal of the American Chemical Society
Carbon dioxide utilization in catalysis
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article

CO 2 Fixation and Release Mediated by Carbonate-Based Coordination Polymers

Yusuke Nishiyama, Satoshi Horike, Kanchana Sotho, Kei Morisato, Ayoub Traverson, Yasuteru Shigeta, Kentaro Kadota, Yuta Hori, Sae Matsui, Yoshitaka Aoyama
article en
1 citations

Abstract

We demonstrate the synthesis of 11 carbonate (CO<sub>3</sub><sup>2-</sup>)-based coordination polymers (CPs) from CO<sub>2</sub> and reveal the structure-property correlation of CO<sub>2</sub> release upon decarbonation. The decarbonation temperatures (<i>T</i><sub>CO2</sub>) are tunable as factors of the electronegativity of metal ions and the coordination numbers of CO<sub>3</sub><sup>2-</sup> within the CP lattices. The structural tunability of CO<sub>3</sub><sup>2-</sup>-based CPs enables high gravimetric CO<sub>2</sub> contents (25-30 wt %) and <i>T</i><sub>CO2</sub> in the low-temperature range where low-grade waste heat can be utilized (170-230 °C). The decarbonation mechanism of CO<sub>3</sub><sup>2-</sup>-based CPs, which produces a discrete metal complex, is revealed by 3D electron diffraction and variable-temperature synchrotron X-ray diffraction.

Journal of the American Chemical SocietyVol. 147(33)
Kanazawa University (JP), JEOL (Japan) (JP), University of Tsukuba (JP), Kyoto University (JP), Division of Materials Science and Engineering (AU), Vidyasirimedhi Institute of Science and Technology (TH), Naval Research Laboratory Information Technology Division
Ministry of Education, Culture, Sports, Science and Technology, Iketani Science and Technology Foundation, Toyota Physical and Chemical Research Institute, Japan Society for the Promotion of Science, Japan Science and Technology Agency
Clean water and sanitation
Openalex Percentile: Top 33%
Carbon dioxide utilization in catalysis
0.70
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