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Alkaline Co(OH)<sub>2</sub>-Decorated 2D Monolayer Titanic Acid Nanosheets for Enhanced Photocatalytic Syngas Production from CO<sub>2</sub>

28

Citations

51

References

2021

Year

Abstract

The difficulty of adsorption and activation of CO<sub>2</sub> at the catalytic site and rapid recombination of photogenerated charge carriers severely restrict the CO<sub>2</sub> conversion efficiency. Here, we fabricate a novel alkaline Co(OH)<sub>2</sub>-decorated ultrathin 2D titanic acid nanosheet (H<sub>2</sub>Ti<sub>6</sub>O<sub>13</sub>) catalyst, which rationally couples the structural and functional merits of ultrathin 2D supports with catalytically active Co species. Alkaline Co(OH)<sub>2</sub> beneficially binds and activates CO<sub>2</sub> molecules, while monolayer H<sub>2</sub>Ti<sub>6</sub>O<sub>13</sub> acts as an electron relay that bridges a photosensitizer with Co(OH)<sub>2</sub> catalytic sites. As such, photoexcited charges can be efficiently channeled from light absorbers to activated CO<sub>2</sub> molecules through the ultrathin hybrid Co(OH)<sub>2</sub>/H<sub>2</sub>Ti<sub>6</sub>O<sub>13</sub> composite, thereby producing syngas (CO/H<sub>2</sub> mixture) from photoreduction of CO<sub>2</sub>. High evolution rates of 56.5 μmol h<sup>-1</sup> for CO and 59.3 μmol h<sup>-1</sup> for H<sub>2</sub> are achieved over optimal Co(OH)<sub>2</sub>/H<sub>2</sub>Ti<sub>6</sub>O<sub>13</sub> by visible light illumination. In addition, the CO/H<sub>2</sub> ratio can be facilely tuned from 1:1 to 1:2.4 by changing the Co(OH)<sub>2</sub> content, thus presenting a feasible approach to controllably synthesize different H<sub>2</sub>/CO mixtures for target applications.

References

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