Synergistic photocatalytic reduction of CO2 enabled by MIL-101(Cr)-TiO2-polyimide nanocomposite membranes

Converting CO 2 into valuable chemicals through photocatalytic reduction is a promising method to achieve carbon neutrality. Nonetheless, the insufficient active sites of photocatalysts lead to low CO 2 reduction efficiency and product selectivity. Taking advantage of the synergistic effect of photocatalytic heterostructures is an effective way to overcome this shortcoming. Here, metal-organic frameworks (MIL-101(Cr))-titanium dioxide (TiO 2 ) staggered gap (type II) heterojunctions were deposited on different woven polyimide (PI) substrates (MIL-101-TiO 2 PI hybrid photocatalysts) via atomic layer deposition and hydrothermal reaction for CO 2 photoreduction. The immobilized photocatalysts on the PI substrates resolved the challenge of separating powdered photocatalysts from liquid products or reactants. The prepared MIL-101(Cr)-TiO 2 PI hybrid photocatalysts displayed synergistic photocatalytic reduction performance towards CO 2 by separating the photogenerated charge carriers. The charge transfer between the heterojunctions and the substrates extended the lifetime of the excited electrons and holes, thereby generating synergy effects and promoting the CO 2 reduction yield. The rougher surface and higher specific area of the PI felt enabled higher loadings of heterojunctions compared with other woven structures of the fabric and mat. As a result, MIL-101(Cr)-TiO 2 PI felts showed multiple reduction pathways over the heterostructures and enhanced photocatalytic performance, with the main product yields of 29.6, 9.2, and 0.8 μmol g −1 h −1 for CO, CH 4 and H 2 , respectively. Meanwhile, CO selectivity of the MIL-101(Cr)-TiO 2 PI felt reached as high as 75%. This study provides significant insights into the role of the substrate in flexible and immobilized hybrid photocatalysts with synergistic performance to achieve enhanced CO 2 reduction performance. • MIL-TiO 2 -PI hybrid catalysts were designed for photocatalytic CO 2 reduction • High roughness and surface area of PI felt substrate provide more MOF growth sites • MIL-TiO 2 -PI felt enhanced CO 2 reduction yield by retaining more heterojunctions • The nanostructured photocatalysts offer an effecetive solution for CO 2 reduction

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Publication Details

Journal
Journal of environmental chemical engineering
Published
2025-06-24
DOI
https://doi.org/10.1016/j.jece.2025.117731
Citations
1
Primary Topic
Advanced Photocatalysis Techniques
Type
article
Field-Weighted Citation Impact
0.36

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article

Synergistic photocatalytic reduction of CO2 enabled by MIL-101(Cr)-TiO2-polyimide nanocomposite membranes

Weilin Xu, Shuaifei Zhao, Lingxue Kong, Joselito M. Razal et al.
1 citations
Journal of environmental chemical engineering
Advanced Photocatalysis Techniques
0.36
article

Synergistic photocatalytic reduction of CO2 enabled by MIL-101(Cr)-TiO2-polyimide nanocomposite membranes

Weilin Xu, Shuaifei Zhao, Lingxue Kong, Joselito M. Razal, Weimin Gao, Milad Laghaei, Lipei Ren, Jiaqi Zhang, Han Wang
article en
1 citations

Abstract

Converting CO 2 into valuable chemicals through photocatalytic reduction is a promising method to achieve carbon neutrality. Nonetheless, the insufficient active sites of photocatalysts lead to low CO 2 reduction efficiency and product selectivity. Taking advantage of the synergistic effect of photocatalytic heterostructures is an effective way to overcome this shortcoming. Here, metal-organic frameworks (MIL-101(Cr))-titanium dioxide (TiO 2 ) staggered gap (type II) heterojunctions were deposited on different woven polyimide (PI) substrates (MIL-101-TiO 2 PI hybrid photocatalysts) via atomic layer deposition and hydrothermal reaction for CO 2 photoreduction. The immobilized photocatalysts on the PI substrates resolved the challenge of separating powdered photocatalysts from liquid products or reactants. The prepared MIL-101(Cr)-TiO 2 PI hybrid photocatalysts displayed synergistic photocatalytic reduction performance towards CO 2 by separating the photogenerated charge carriers. The charge transfer between the heterojunctions and the substrates extended the lifetime of the excited electrons and holes, thereby generating synergy effects and promoting the CO 2 reduction yield. The rougher surface and higher specific area of the PI felt enabled higher loadings of heterojunctions compared with other woven structures of the fabric and mat. As a result, MIL-101(Cr)-TiO 2 PI felts showed multiple reduction pathways over the heterostructures and enhanced photocatalytic performance, with the main product yields of 29.6, 9.2, and 0.8 μmol g −1 h −1 for CO, CH 4 and H 2 , respectively. Meanwhile, CO selectivity of the MIL-101(Cr)-TiO 2 PI felt reached as high as 75%. This study provides significant insights into the role of the substrate in flexible and immobilized hybrid photocatalysts with synergistic performance to achieve enhanced CO 2 reduction performance. • MIL-TiO 2 -PI hybrid catalysts were designed for photocatalytic CO 2 reduction • High roughness and surface area of PI felt substrate provide more MOF growth sites • MIL-TiO 2 -PI felt enhanced CO 2 reduction yield by retaining more heterojunctions • The nanostructured photocatalysts offer an effecetive solution for CO 2 reduction

Journal of environmental chemical engineeringVol. 13(5)
North China University of Science and Technology (CN), Deakin University (AU), Wuhan Textile University (CN), RMIT University (AU)
Australian Research Council
Openalex Percentile: Top 42%
Advanced Photocatalysis Techniques
0.36
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