A Ni-O-Ag photothermal catalyst enables 103-m <sup>2</sup> artificial photosynthesis with >17% solar-to-chemical energy conversion efficiency
Article 2024 en
Authors
YL
Yaguang Li
FM
Fanqi Meng
QW
Qixuan Wu
Abstract
1 min read
The scalable artificial photosynthesis composed of photovoltaic electrolysis and photothermal catalysis is limited by inefficient photothermal CO<sub>2</sub> hydrogenation under weak sunlight irradiation. Herein, NiO nanosheets supported with Ag single atoms [two-dimensional (2D) Ni<sub>1</sub>Ag<sub>0.02</sub>O<sub>1</sub>] are synthesized for photothermal CO<sub>2</sub> hydrogenation to achieve 1065 mmol g<sup>-1</sup> hour<sup>-1</sup> of CO production rate under 1-sun irradiation. This performance is attributed to the coupling effect of Ag-O-Ni sites to enhance the hydrogenation of CO<sub>2</sub> and weaken the CO adsorption, resulting in 1434 mmol g<sup>-1</sup> hour<sup>-1</sup> of CO yield at 300°C. Furthermore, we integrate the 2D Ni<sub>1</sub>Ag<sub>0.02</sub>O<sub>1</sub>-supported photothermal reverse water-gas shift reaction with commercial photovoltaic electrolytic water splitting to construct a 103-m<sup>2</sup> scale artificial photosynthesis system (CO<sub>2</sub> + H<sub>2</sub>O → CO + H<sub>2</sub> + O<sub>2</sub>), which achieves more than 22 m<sup>3</sup>/day of green syngas with an adjustable H<sub>2</sub>/CO ratio (0.4-3) and a photochemical energy conversion efficiency of >17%. This research charts a promising course for designing practical, natural sunlight-driven artificial photosynthesis systems.
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