{"title":"固体氧化物电解池中La0.5Ce0.5Fe0.5Ni0.5O3−δ阳极的电化学甲烷重整","authors":"Wenxin Fu, Yige Guo, Jianqiu Zhu, Xiaomin Zhang, Linjuan Zhang, Yuefeng Song, Guoxiong Wang, Xinhe Bao","doi":"10.1021/acsami.5c01874","DOIUrl":null,"url":null,"abstract":"Coupling the partial oxidation of methane (POM) to the anode of solid oxide electrolysis cells (SOECs) can significantly decrease the open-circuit voltage and electrical energy consumption of the SOECs. However, developing advanced anode for SOEC to selectively convert CH<sub>4</sub> to syngas still remains a great challenge. Herein, we find that Ce substitution at the A-site of La<sub>0.5</sub>Ce<sub>0.5</sub>Fe<sub>0.5</sub>Ni<sub>0.5</sub>O<sub>3−δ</sub> can effectively alter the chemical state and coordination environment of Ni with the generation of NiO particles, and the air activation could further regulate the oxygen vacancy concentration and decrease the size of NiO particles, which both contribute to the enhanced POM performance with CH<sub>4</sub> conversion of 45.20% and CO selectivity of 92.67% at 650 °C. Moreover, the introduction of POM to the anode could remarkably decrease the electrical energy consumption for CO production from 3.64 kWh m<sup>–3</sup> of conventional SOECs to 0.86 kWh m<sup>–3</sup> of CH<sub>4</sub>-assisted SOECs. This study provides an effective strategy for improving the electrochemical performance of CO<sub>2</sub> electrolysis in SOECs while simultaneously converting CH<sub>4</sub> to syngas at the anode.","PeriodicalId":5,"journal":{"name":"ACS Applied Materials & Interfaces","volume":"53 1","pages":""},"PeriodicalIF":8.3000,"publicationDate":"2025-04-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Electrochemical Methane Reforming on La0.5Ce0.5Fe0.5Ni0.5O3−δ Anode in Solid Oxide Electrolysis Cells\",\"authors\":\"Wenxin Fu, Yige Guo, Jianqiu Zhu, Xiaomin Zhang, Linjuan Zhang, Yuefeng Song, Guoxiong Wang, Xinhe Bao\",\"doi\":\"10.1021/acsami.5c01874\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Coupling the partial oxidation of methane (POM) to the anode of solid oxide electrolysis cells (SOECs) can significantly decrease the open-circuit voltage and electrical energy consumption of the SOECs. However, developing advanced anode for SOEC to selectively convert CH<sub>4</sub> to syngas still remains a great challenge. Herein, we find that Ce substitution at the A-site of La<sub>0.5</sub>Ce<sub>0.5</sub>Fe<sub>0.5</sub>Ni<sub>0.5</sub>O<sub>3−δ</sub> can effectively alter the chemical state and coordination environment of Ni with the generation of NiO particles, and the air activation could further regulate the oxygen vacancy concentration and decrease the size of NiO particles, which both contribute to the enhanced POM performance with CH<sub>4</sub> conversion of 45.20% and CO selectivity of 92.67% at 650 °C. Moreover, the introduction of POM to the anode could remarkably decrease the electrical energy consumption for CO production from 3.64 kWh m<sup>–3</sup> of conventional SOECs to 0.86 kWh m<sup>–3</sup> of CH<sub>4</sub>-assisted SOECs. This study provides an effective strategy for improving the electrochemical performance of CO<sub>2</sub> electrolysis in SOECs while simultaneously converting CH<sub>4</sub> to syngas at the anode.\",\"PeriodicalId\":5,\"journal\":{\"name\":\"ACS Applied Materials & Interfaces\",\"volume\":\"53 1\",\"pages\":\"\"},\"PeriodicalIF\":8.3000,\"publicationDate\":\"2025-04-25\",\"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.5c01874\",\"RegionNum\":2,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"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.5c01874","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
Electrochemical Methane Reforming on La0.5Ce0.5Fe0.5Ni0.5O3−δ Anode in Solid Oxide Electrolysis Cells
Coupling the partial oxidation of methane (POM) to the anode of solid oxide electrolysis cells (SOECs) can significantly decrease the open-circuit voltage and electrical energy consumption of the SOECs. However, developing advanced anode for SOEC to selectively convert CH4 to syngas still remains a great challenge. Herein, we find that Ce substitution at the A-site of La0.5Ce0.5Fe0.5Ni0.5O3−δ can effectively alter the chemical state and coordination environment of Ni with the generation of NiO particles, and the air activation could further regulate the oxygen vacancy concentration and decrease the size of NiO particles, which both contribute to the enhanced POM performance with CH4 conversion of 45.20% and CO selectivity of 92.67% at 650 °C. Moreover, the introduction of POM to the anode could remarkably decrease the electrical energy consumption for CO production from 3.64 kWh m–3 of conventional SOECs to 0.86 kWh m–3 of CH4-assisted SOECs. This study provides an effective strategy for improving the electrochemical performance of CO2 electrolysis in SOECs while simultaneously converting CH4 to syngas at the anode.
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.