Tetraperoxotitanates for High-Capacity Direct Air Capture of Carbon Dioxide

Materials chemists play a strategic role in achieving ambitious global climate goals, including removing legacy CO2 via direct air capture (DAC). Innovating diverse DAC materials will enable their effective use in varying conditions and improve our understanding of CO2 capture mechanisms. In our current contribution, we have synthesized a family of homoleptic alkali tetraperoxotitanate materials (generally formulated A4Ti(O2)4, A = Li, Na, or K) and studied their DAC reactivity. Synthesis was achieved with inexpensive reagents and >90% yields. We present the first single-crystal X-ray structures (five total) of A4Ti(O2)4 compounds along with supplemental bulk characterization and computation. We compare their DAC behavior in simple ambient benchtop experiments, determining CO2 uptake by combustion analysis of postcapture materials. The K analogue exhibited the most rapid and high-capacity DAC, 8.17 mmol CO2/g sorbent, translating to nearly 3 mol CO2 per mole Ti and reaching near maximum capacity in under 10 days. The Li and Na analogues exhibit delayed reactivity along with high DAC capacity (6.66 and 8.18 mmol of CO2/g sorbent, respectively). Characterization of the DAC products via scanning electron microscopy shows phase separation of alkali-rich and Ti-rich regions in core–shell morphologies for the Na and Li analogues; this is discussed with respect to the role of titanium vs alkali in DAC. On the other hand, no phase separation was observed for the K analogue. In situ monitoring detailed the early-stage CO2 capture behavior of the K analogue, reaching ∼50% of maximum capacity within 1 h. The differentiating behavior of the K analogue is attributed to its unique composition, containing four H2O2 lattice molecules in addition to the four O2– peroxide anions bonded to TiIV. While H2O2 (aq) alone does not exhibit CO2 chemisorption, the basic environment of the A4Ti(O2)4 lattice activates its rapid DAC, inspiring the future exploration of peroxosolvate materials for DAC.

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Publication Details

Journal
Chemistry of Materials
Published
2024-12-12
DOI
https://doi.org/10.1021/acs.chemmater.4c01795
Citations
2
Primary Topic
Carbon Dioxide Capture Technologies
Type
article
Field-Weighted Citation Impact
0.43

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article

Tetraperoxotitanates for High-Capacity Direct Air Capture of Carbon Dioxide

Eduard Garrido Ribó, Makenzie T. Nord, Konstantinos A. Goulas, Tim Joachim Zuehlsdorff et al.
2 citations
Chemistry of Materials
Carbon Dioxide Capture Technologies
0.43
article

Tetraperoxotitanates for High-Capacity Direct Air Capture of Carbon Dioxide

Eduard Garrido Ribó, Makenzie T. Nord, Konstantinos A. Goulas, Tim Joachim Zuehlsdorff, May Nyman, Jacob S. Hirschi, Lev N. Zakharov, Karlie Bach, Zhiwei Mao
article en
2 citations

Abstract

Materials chemists play a strategic role in achieving ambitious global climate goals, including removing legacy CO2 via direct air capture (DAC). Innovating diverse DAC materials will enable their effective use in varying conditions and improve our understanding of CO2 capture mechanisms. In our current contribution, we have synthesized a family of homoleptic alkali tetraperoxotitanate materials (generally formulated A4Ti(O2)4, A = Li, Na, or K) and studied their DAC reactivity. Synthesis was achieved with inexpensive reagents and >90% yields. We present the first single-crystal X-ray structures (five total) of A4Ti(O2)4 compounds along with supplemental bulk characterization and computation. We compare their DAC behavior in simple ambient benchtop experiments, determining CO2 uptake by combustion analysis of postcapture materials. The K analogue exhibited the most rapid and high-capacity DAC, 8.17 mmol CO2/g sorbent, translating to nearly 3 mol CO2 per mole Ti and reaching near maximum capacity in under 10 days. The Li and Na analogues exhibit delayed reactivity along with high DAC capacity (6.66 and 8.18 mmol of CO2/g sorbent, respectively). Characterization of the DAC products via scanning electron microscopy shows phase separation of alkali-rich and Ti-rich regions in core–shell morphologies for the Na and Li analogues; this is discussed with respect to the role of titanium vs alkali in DAC. On the other hand, no phase separation was observed for the K analogue. In situ monitoring detailed the early-stage CO2 capture behavior of the K analogue, reaching ∼50% of maximum capacity within 1 h. The differentiating behavior of the K analogue is attributed to its unique composition, containing four H2O2 lattice molecules in addition to the four O2– peroxide anions bonded to TiIV. While H2O2 (aq) alone does not exhibit CO2 chemisorption, the basic environment of the A4Ti(O2)4 lattice activates its rapid DAC, inspiring the future exploration of peroxosolvate materials for DAC.

Chemistry of MaterialsVol. 37(1)
Oregon State University (US)
U.S. Department of Energy
Openalex Percentile: Top 40%
Carbon Dioxide Capture Technologies
0.43
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