Arturo Sanz-Marco, Javier Navarro-Ruiz, Jose L. Hueso, Iann C. Gerber, Victor Sebastian, Susanne Mossin, David Nielsen, Francisco Balas, Jesus Santamaria
{"title":"紫外-红外连续光催化ni掺杂氧化硫化钼气相CO2加氢:实验与机理研究","authors":"Arturo Sanz-Marco, Javier Navarro-Ruiz, Jose L. Hueso, Iann C. Gerber, Victor Sebastian, Susanne Mossin, David Nielsen, Francisco Balas, Jesus Santamaria","doi":"10.1002/cey2.685","DOIUrl":null,"url":null,"abstract":"<p>The reduction of CO<sub>2</sub> toward CO and CH<sub>4</sub> over Ni-loaded MoS<sub>2</sub>-like layered nanomaterials is investigated. The mild hydrothermal synthesis induced the formation of a molybdenum oxysulfide (MoO<sub><i>x</i></sub>S<sub><i>y</i></sub>) phase, enriched with sulfur defects and multiple Mo oxidation states that favor the insertion of Ni<sup>2+</sup> cations via photo-assisted precipitation. The photocatalytic tests under LED irradiation at different wavelengths from 365 to 940 nm at 250°C rendered 1% CO<sub>2</sub> conversion and continuous CO production up to 0.6 mmol/(g<sub>cat</sub> h). The incorporation of Ni into the MoO<sub><i>x</i></sub>S<sub><i>y</i></sub> structure boosted the continuous production of CO up to 5.1 mmol/(g<sub>cat</sub> h) with a CO<sub>2</sub> conversion of 3.5%. In situ spectroscopic techniques and DFT simulations showed the O-incorporated MoS<sub>2</sub> structure, in addition to Ni clusters as a supported metal catalyst. The mechanistic study of the CO<sub>2</sub> reduction reaction over the catalysts revealed that the reverse water–gas shift reaction is favored due to the preferential formation of carboxylic species.</p>","PeriodicalId":33706,"journal":{"name":"Carbon Energy","volume":"7 4","pages":""},"PeriodicalIF":24.2000,"publicationDate":"2025-02-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cey2.685","citationCount":"0","resultStr":"{\"title\":\"UV to IR Continuous Photocatalytic Gas-Phase CO2 Hydrogenation Over Ni-Doped Molybdenum Oxysulfide: An Experimental and Mechanistic Study\",\"authors\":\"Arturo Sanz-Marco, Javier Navarro-Ruiz, Jose L. Hueso, Iann C. Gerber, Victor Sebastian, Susanne Mossin, David Nielsen, Francisco Balas, Jesus Santamaria\",\"doi\":\"10.1002/cey2.685\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>The reduction of CO<sub>2</sub> toward CO and CH<sub>4</sub> over Ni-loaded MoS<sub>2</sub>-like layered nanomaterials is investigated. The mild hydrothermal synthesis induced the formation of a molybdenum oxysulfide (MoO<sub><i>x</i></sub>S<sub><i>y</i></sub>) phase, enriched with sulfur defects and multiple Mo oxidation states that favor the insertion of Ni<sup>2+</sup> cations via photo-assisted precipitation. The photocatalytic tests under LED irradiation at different wavelengths from 365 to 940 nm at 250°C rendered 1% CO<sub>2</sub> conversion and continuous CO production up to 0.6 mmol/(g<sub>cat</sub> h). The incorporation of Ni into the MoO<sub><i>x</i></sub>S<sub><i>y</i></sub> structure boosted the continuous production of CO up to 5.1 mmol/(g<sub>cat</sub> h) with a CO<sub>2</sub> conversion of 3.5%. In situ spectroscopic techniques and DFT simulations showed the O-incorporated MoS<sub>2</sub> structure, in addition to Ni clusters as a supported metal catalyst. The mechanistic study of the CO<sub>2</sub> reduction reaction over the catalysts revealed that the reverse water–gas shift reaction is favored due to the preferential formation of carboxylic species.</p>\",\"PeriodicalId\":33706,\"journal\":{\"name\":\"Carbon Energy\",\"volume\":\"7 4\",\"pages\":\"\"},\"PeriodicalIF\":24.2000,\"publicationDate\":\"2025-02-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cey2.685\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Carbon Energy\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/cey2.685\",\"RegionNum\":1,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Carbon Energy","FirstCategoryId":"88","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cey2.685","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
UV to IR Continuous Photocatalytic Gas-Phase CO2 Hydrogenation Over Ni-Doped Molybdenum Oxysulfide: An Experimental and Mechanistic Study
The reduction of CO2 toward CO and CH4 over Ni-loaded MoS2-like layered nanomaterials is investigated. The mild hydrothermal synthesis induced the formation of a molybdenum oxysulfide (MoOxSy) phase, enriched with sulfur defects and multiple Mo oxidation states that favor the insertion of Ni2+ cations via photo-assisted precipitation. The photocatalytic tests under LED irradiation at different wavelengths from 365 to 940 nm at 250°C rendered 1% CO2 conversion and continuous CO production up to 0.6 mmol/(gcat h). The incorporation of Ni into the MoOxSy structure boosted the continuous production of CO up to 5.1 mmol/(gcat h) with a CO2 conversion of 3.5%. In situ spectroscopic techniques and DFT simulations showed the O-incorporated MoS2 structure, in addition to Ni clusters as a supported metal catalyst. The mechanistic study of the CO2 reduction reaction over the catalysts revealed that the reverse water–gas shift reaction is favored due to the preferential formation of carboxylic species.
期刊介绍:
Carbon Energy is an international journal that focuses on cutting-edge energy technology involving carbon utilization and carbon emission control. It provides a platform for researchers to communicate their findings and critical opinions and aims to bring together the communities of advanced material and energy. The journal covers a broad range of energy technologies, including energy storage, photocatalysis, electrocatalysis, photoelectrocatalysis, and thermocatalysis. It covers all forms of energy, from conventional electric and thermal energy to those that catalyze chemical and biological transformations. Additionally, Carbon Energy promotes new technologies for controlling carbon emissions and the green production of carbon materials. The journal welcomes innovative interdisciplinary research with wide impact. It is indexed in various databases, including Advanced Technologies & Aerospace Collection/Database, Biological Science Collection/Database, CAS, DOAJ, Environmental Science Collection/Database, Web of Science and Technology Collection.