{"title":"mo修饰氧化铈†上逆水气转换的光诱导增强","authors":"Daichi Takami , Naoto Doshita , Ryosuke Sugiura , Yasutaka Kuwahara , Hiromi Yamashita","doi":"10.1039/d5cy00597c","DOIUrl":null,"url":null,"abstract":"<div><div>The reverse water–gas shift (RWGS) reaction, converting CO<sub>2</sub> into CO, is a promising approach for sustainable carbon utilization. However, high energy demand poses significant barriers to its practical application. Here, we report the development of platinum-loaded metal-modified cerium oxide catalysts (Pt/M<sub><em>x</em></sub>Ce<sub>1−<em>x</em></sub>O<sub><em>y</em></sub>), designed to enhance RWGS reaction efficiency through photocatalytic and photothermal catalytic approaches, aiming at solar light utilization. Mo-modified catalysts exhibited a high CO formation rate of 10.2 mmol g<sup>−1</sup> h<sup>−1</sup> at 473 K in the dark and 23.5 mmol g<sup>−1</sup> h<sup>−1</sup> under visible and near-infrared light irradiation, which outperformed the catalytic activity of the pristine Pt/CeO<sub><em>y</em></sub> catalyst. Detailed characterization revealed that Mo doping improved CO<sub>2</sub> adsorption and dissociation capability. Moreover, under visible-NIR light irradiation, the catalyst performance further improved due to thermal and non-thermal effects of light irradiation. These findings highlight a dual enhancement mechanism—light-induced thermal and non-thermal pathways—that significantly boosts catalytic efficiency. This study provides valuable insights into designing advanced light-responsive catalysts, offering a promising pathway toward efficient and sustainable CO<sub>2</sub> conversion technologies.</div></div>","PeriodicalId":66,"journal":{"name":"Catalysis Science & Technology","volume":"15 18","pages":"Pages 5285-5294"},"PeriodicalIF":4.2000,"publicationDate":"2025-06-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Photo-induced enhancement of reverse water–gas shift over Mo-modified cerium oxide†\",\"authors\":\"Daichi Takami , Naoto Doshita , Ryosuke Sugiura , Yasutaka Kuwahara , Hiromi Yamashita\",\"doi\":\"10.1039/d5cy00597c\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The reverse water–gas shift (RWGS) reaction, converting CO<sub>2</sub> into CO, is a promising approach for sustainable carbon utilization. However, high energy demand poses significant barriers to its practical application. Here, we report the development of platinum-loaded metal-modified cerium oxide catalysts (Pt/M<sub><em>x</em></sub>Ce<sub>1−<em>x</em></sub>O<sub><em>y</em></sub>), designed to enhance RWGS reaction efficiency through photocatalytic and photothermal catalytic approaches, aiming at solar light utilization. Mo-modified catalysts exhibited a high CO formation rate of 10.2 mmol g<sup>−1</sup> h<sup>−1</sup> at 473 K in the dark and 23.5 mmol g<sup>−1</sup> h<sup>−1</sup> under visible and near-infrared light irradiation, which outperformed the catalytic activity of the pristine Pt/CeO<sub><em>y</em></sub> catalyst. Detailed characterization revealed that Mo doping improved CO<sub>2</sub> adsorption and dissociation capability. Moreover, under visible-NIR light irradiation, the catalyst performance further improved due to thermal and non-thermal effects of light irradiation. These findings highlight a dual enhancement mechanism—light-induced thermal and non-thermal pathways—that significantly boosts catalytic efficiency. This study provides valuable insights into designing advanced light-responsive catalysts, offering a promising pathway toward efficient and sustainable CO<sub>2</sub> conversion technologies.</div></div>\",\"PeriodicalId\":66,\"journal\":{\"name\":\"Catalysis Science & Technology\",\"volume\":\"15 18\",\"pages\":\"Pages 5285-5294\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2025-06-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Catalysis Science & Technology\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S2044475325003521\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Catalysis Science & Technology","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S2044475325003521","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Photo-induced enhancement of reverse water–gas shift over Mo-modified cerium oxide†
The reverse water–gas shift (RWGS) reaction, converting CO2 into CO, is a promising approach for sustainable carbon utilization. However, high energy demand poses significant barriers to its practical application. Here, we report the development of platinum-loaded metal-modified cerium oxide catalysts (Pt/MxCe1−xOy), designed to enhance RWGS reaction efficiency through photocatalytic and photothermal catalytic approaches, aiming at solar light utilization. Mo-modified catalysts exhibited a high CO formation rate of 10.2 mmol g−1 h−1 at 473 K in the dark and 23.5 mmol g−1 h−1 under visible and near-infrared light irradiation, which outperformed the catalytic activity of the pristine Pt/CeOy catalyst. Detailed characterization revealed that Mo doping improved CO2 adsorption and dissociation capability. Moreover, under visible-NIR light irradiation, the catalyst performance further improved due to thermal and non-thermal effects of light irradiation. These findings highlight a dual enhancement mechanism—light-induced thermal and non-thermal pathways—that significantly boosts catalytic efficiency. This study provides valuable insights into designing advanced light-responsive catalysts, offering a promising pathway toward efficient and sustainable CO2 conversion technologies.
期刊介绍:
A multidisciplinary journal focusing on cutting edge research across all fundamental science and technological aspects of catalysis.
Editor-in-chief: Bert Weckhuysen
Impact factor: 5.0
Time to first decision (peer reviewed only): 31 days