Fei Liu, Pengfei Li, Zoufei Du, Lidan Lan, Haijiao Xie, Yi Dan, Yun Huang, Long Jiang
{"title":"极化诱导内电场主导S-Scheme KNbO3-CuO异质结光还原CO2的高CH4选择性。","authors":"Fei Liu, Pengfei Li, Zoufei Du, Lidan Lan, Haijiao Xie, Yi Dan, Yun Huang, Long Jiang","doi":"10.1021/acsami.4c16163","DOIUrl":null,"url":null,"abstract":"<p><p>The polarization-induced internal electric field (IEF) in ferroelectric materials could promote photogenerated charge transfer across the heterojunction interface, but the effect of polarization-induced IEF on the mechanism of photogenerated charge transfer is ambiguous. In this study, a KNbO<sub>3</sub>-CuO heterojunction was synthesized by depositing copper oxide (CuO) onto KNbO<sub>3</sub>. Incorporating CuO broadens the light absorption of KNbO<sub>3</sub>, thereby enhancing the dissociation of the photogenerated charges. The results show that the polarization-induced IEF in KNbO<sub>3</sub> determines that the charge transport mechanism in the KNbO<sub>3</sub>-CuO heterojunction follows the S-scheme. Owing to the S-scheme heterojunctions and efficient CO<sub>2</sub> capture and activation by CuO, the CH<sub>4</sub> production rate of KNbO<sub>3</sub>-CuO increased by nearly 26 times compared to KNbO<sub>3</sub>. Additionally, the CH<sub>4</sub> selectivity of KNbO<sub>3</sub>-CuO could reach up to 97.80%. This research offers valuable insights into enhancing the photogenerated charge separation and constructing heterojunctions.</p>","PeriodicalId":5,"journal":{"name":"ACS Applied Materials & Interfaces","volume":" ","pages":"69418-69429"},"PeriodicalIF":8.3000,"publicationDate":"2024-12-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Polarization-Induced Internal Electric Field-Dominated S-Scheme KNbO<sub>3</sub>-CuO Heterojunction for Photoreduction of CO<sub>2</sub> with High CH<sub>4</sub> Selectivity.\",\"authors\":\"Fei Liu, Pengfei Li, Zoufei Du, Lidan Lan, Haijiao Xie, Yi Dan, Yun Huang, Long Jiang\",\"doi\":\"10.1021/acsami.4c16163\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The polarization-induced internal electric field (IEF) in ferroelectric materials could promote photogenerated charge transfer across the heterojunction interface, but the effect of polarization-induced IEF on the mechanism of photogenerated charge transfer is ambiguous. In this study, a KNbO<sub>3</sub>-CuO heterojunction was synthesized by depositing copper oxide (CuO) onto KNbO<sub>3</sub>. Incorporating CuO broadens the light absorption of KNbO<sub>3</sub>, thereby enhancing the dissociation of the photogenerated charges. The results show that the polarization-induced IEF in KNbO<sub>3</sub> determines that the charge transport mechanism in the KNbO<sub>3</sub>-CuO heterojunction follows the S-scheme. Owing to the S-scheme heterojunctions and efficient CO<sub>2</sub> capture and activation by CuO, the CH<sub>4</sub> production rate of KNbO<sub>3</sub>-CuO increased by nearly 26 times compared to KNbO<sub>3</sub>. Additionally, the CH<sub>4</sub> selectivity of KNbO<sub>3</sub>-CuO could reach up to 97.80%. This research offers valuable insights into enhancing the photogenerated charge separation and constructing heterojunctions.</p>\",\"PeriodicalId\":5,\"journal\":{\"name\":\"ACS Applied Materials & Interfaces\",\"volume\":\" \",\"pages\":\"69418-69429\"},\"PeriodicalIF\":8.3000,\"publicationDate\":\"2024-12-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Materials & Interfaces\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1021/acsami.4c16163\",\"RegionNum\":2,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/12/4 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"MATERIALS SCIENCE, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Materials & Interfaces","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1021/acsami.4c16163","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/12/4 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
Polarization-Induced Internal Electric Field-Dominated S-Scheme KNbO3-CuO Heterojunction for Photoreduction of CO2 with High CH4 Selectivity.
The polarization-induced internal electric field (IEF) in ferroelectric materials could promote photogenerated charge transfer across the heterojunction interface, but the effect of polarization-induced IEF on the mechanism of photogenerated charge transfer is ambiguous. In this study, a KNbO3-CuO heterojunction was synthesized by depositing copper oxide (CuO) onto KNbO3. Incorporating CuO broadens the light absorption of KNbO3, thereby enhancing the dissociation of the photogenerated charges. The results show that the polarization-induced IEF in KNbO3 determines that the charge transport mechanism in the KNbO3-CuO heterojunction follows the S-scheme. Owing to the S-scheme heterojunctions and efficient CO2 capture and activation by CuO, the CH4 production rate of KNbO3-CuO increased by nearly 26 times compared to KNbO3. Additionally, the CH4 selectivity of KNbO3-CuO could reach up to 97.80%. This research offers valuable insights into enhancing the photogenerated charge separation and constructing heterojunctions.
期刊介绍:
ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.