{"title":"Tailoring CuFeO<sub>x</sub>-Based Catalytic Oxygen Carrier for Lattice Oxygen-Induced Oxidative Steam Reforming of Methanol.","authors":"Feng Tan, Zhiqiang Sun","doi":"10.1002/cssc.202500599","DOIUrl":null,"url":null,"abstract":"<p><p>Methanol reforming demonstrates the possibility of realizing hydrogen storage, transport, and on-site supply. Nevertheless, this approach faces limitations due to outlet CO generation and catalyst degradation. This work fabricates a series of CuFeO<sub>x</sub>-based catalytic oxygen carriers (COC) with various Cu-to-Fe ratios for lattice oxygen-induced methanol reforming, which goes through lattice oxygen-induced methanol reforming → catalytic steam methanol reforming → oxidative steam methanol reforming. It is revealed that the lattice oxygen mobility can be tuned by modulating the Cu-to-Fe mole ratios. Of the synthesized COCs, Cu<sub>2</sub>Fe<sub>3</sub> shows the highest catalytic activity. It is supposed that CuO in COC provides lattice oxygen with catalytically site of Cu<sup>0</sup>, while CuFe<sub>5</sub>O<sub>8</sub> contributes relatively stable Cu<sup>+</sup>, synergistically inducing highly efficient oxidative steam reforming of methanol. Specifically, a H<sub>2</sub> production rate of 93.9 mmol·H<sub>2</sub>·h<sup>-1</sup> g<sup>-1</sup>·COC·at 220 °C is achieved with relatively stable redox looping within 20 cycles. The in situ diffuse reflectance infrared Fourier transform spectroscopy results indicate that the bridged formate species is identified as the primary intermediate under lattice oxygen-induced conditions, and the reaction pathway is anticipated to be CH<sub>3</sub>OH* → CH<sub>3</sub>O* → CH<sub>2</sub>O* → HCOO* → H<sub>2</sub> + CO<sub>2</sub>.</p>","PeriodicalId":149,"journal":{"name":"ChemSusChem","volume":" ","pages":"e2500599"},"PeriodicalIF":7.5000,"publicationDate":"2025-05-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemSusChem","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/cssc.202500599","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Methanol reforming demonstrates the possibility of realizing hydrogen storage, transport, and on-site supply. Nevertheless, this approach faces limitations due to outlet CO generation and catalyst degradation. This work fabricates a series of CuFeOx-based catalytic oxygen carriers (COC) with various Cu-to-Fe ratios for lattice oxygen-induced methanol reforming, which goes through lattice oxygen-induced methanol reforming → catalytic steam methanol reforming → oxidative steam methanol reforming. It is revealed that the lattice oxygen mobility can be tuned by modulating the Cu-to-Fe mole ratios. Of the synthesized COCs, Cu2Fe3 shows the highest catalytic activity. It is supposed that CuO in COC provides lattice oxygen with catalytically site of Cu0, while CuFe5O8 contributes relatively stable Cu+, synergistically inducing highly efficient oxidative steam reforming of methanol. Specifically, a H2 production rate of 93.9 mmol·H2·h-1 g-1·COC·at 220 °C is achieved with relatively stable redox looping within 20 cycles. The in situ diffuse reflectance infrared Fourier transform spectroscopy results indicate that the bridged formate species is identified as the primary intermediate under lattice oxygen-induced conditions, and the reaction pathway is anticipated to be CH3OH* → CH3O* → CH2O* → HCOO* → H2 + CO2.
期刊介绍:
ChemSusChem
Impact Factor (2016): 7.226
Scope:
Interdisciplinary journal
Focuses on research at the interface of chemistry and sustainability
Features the best research on sustainability and energy
Areas Covered:
Chemistry
Materials Science
Chemical Engineering
Biotechnology