{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["4(16)"],"submitter":["Song L"],"pubmed_abstract":["Solar-driven CO<sub>2</sub> conversion into the industrial chemical CO <i>via</i> the reverse water-gas reaction is an ideal technological approach to achieve the key step of carbon neutralization. The high reaction temperature is cost-free due to the photothermal conversion brought about by solar irradiation and is beneficial to the catalytic efficiency. However, the thermostability of adopted catalysts is a great challenge. Herein, we develop an <i>in situ</i> photothermal synthesis to obtain a CuO <sub><i>x</i></sub> &FeO <sub><i>y</i></sub> catalyst with a layered double hydroxide-derived pore-confined frame. The optimized sample delivers a CO generation rate of 136.3 mmol min<sup>-1</sup> g<sub>cat</sub> <sup>-1</sup> with the selectivity of ∼100% at a high reaction temperature of 101"],"journal":["Nanoscale advances"],"pagination":["3391-3397"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9419767"],"repository":["biostudies-literature"],"pubmed_title":["Photothermal synthesis of a CuO <sub><i>x</i></sub> &FeO <sub><i>y</i></sub> catalyst with a layered double hydroxide-derived pore-confined frame to achieve photothermal CO<sub>2</sub> hydrogenation to CO with a rate of 136 mmol min<sup>-1</sup> g<sub>cat</sub> <sup>-1</sup>."],"pmcid":["PMC9419767"],"pubmed_authors":["Song L","Ouyang S","Yi X","Ye J"],"additional_accession":[]},"is_claimable":false,"name":"Photothermal synthesis of a CuO <sub><i>x</i></sub> &FeO <sub><i>y</i></sub> catalyst with a layered double hydroxide-derived pore-confined frame to achieve photothermal CO<sub>2</sub> hydrogenation to CO with a rate of 136 mmol min<sup>-1</sup> g<sub>cat</sub> <sup>-1</sup>.","description":"Solar-driven CO<sub>2</sub> conversion into the industrial chemical CO <i>via</i> the reverse water-gas reaction is an ideal technological approach to achieve the key step of carbon neutralization. The high reaction temperature is cost-free due to the photothermal conversion brought about by solar irradiation and is beneficial to the catalytic efficiency. However, the thermostability of adopted catalysts is a great challenge. Herein, we develop an <i>in situ</i> photothermal synthesis to obtain a CuO <sub><i>x</i></sub> &FeO <sub><i>y</i></sub> catalyst with a layered double hydroxide-derived pore-confined frame. The optimized sample delivers a CO generation rate of 136.3 mmol min<sup>-1</sup> g<sub>cat</sub> <sup>-1</sup> with the selectivity of ∼100% at a high reaction temperature of 101","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Aug","modification":"2025-04-18T15:47:29.572Z","creation":"2024-11-20T05:32:33.261Z"},"accession":"S-EPMC9419767","cross_references":{"pubmed":["36131705"],"doi":["10.1039/d2na00315e"]}}