Synergistic effects of interface and valence state on boosting electrochemical CO2 reduction activity of La2CuO4
The electrochemical CO2 reduction reaction (CER) to methane (CH4) has received great attention. Here, we proposed an efficient method to facilitate the conversion of CO2-to-CH4 by creating a two-phase interface over urea-modified La2CuO4 catalyst. The most optimized one exhibits the highest selectiv...
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Elsevier
2024-01-01
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Series: | Catalysis Communications |
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Online Access: | http://www.sciencedirect.com/science/article/pii/S1566736723002388 |
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author | Shiya Bian Xuekun Jin Jinxing Mi Fengjuan Chen Li Cai Ziyu Wang Junhua Li Jianjun Chen |
author_facet | Shiya Bian Xuekun Jin Jinxing Mi Fengjuan Chen Li Cai Ziyu Wang Junhua Li Jianjun Chen |
author_sort | Shiya Bian |
collection | DOAJ |
description | The electrochemical CO2 reduction reaction (CER) to methane (CH4) has received great attention. Here, we proposed an efficient method to facilitate the conversion of CO2-to-CH4 by creating a two-phase interface over urea-modified La2CuO4 catalyst. The most optimized one exhibits the highest selectivity (22%) for CH4 and the best activity (14 mA cm−2) and stability (5 h) at the potential of −1 V vs. reversible hydrogen electrode. The enhanced CER performance can be attributed to the establishment of interfacial effect within the two-phase, which facilitates the reduction of Cu2+ and promotes the active sites concentration. |
first_indexed | 2024-03-08T16:32:16Z |
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institution | Directory Open Access Journal |
issn | 1873-3905 |
language | English |
last_indexed | 2024-03-08T16:32:16Z |
publishDate | 2024-01-01 |
publisher | Elsevier |
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series | Catalysis Communications |
spelling | doaj.art-6467b68833ce4005be3126f69b6eb98d2024-01-06T04:38:39ZengElsevierCatalysis Communications1873-39052024-01-01186106836Synergistic effects of interface and valence state on boosting electrochemical CO2 reduction activity of La2CuO4Shiya Bian0Xuekun Jin1Jinxing Mi2Fengjuan Chen3Li Cai4Ziyu Wang5Junhua Li6Jianjun Chen7Key Laboratory of Solid State Physics and Devices Autonomous Region, School of Physics Science and Technology, Xinjiang University, Urumqi 830046, Xinjiang, P. R. China; Key Laboratory of Energy Materials Chemistry, Ministry of Education, Institute of Applied Chemistry, Xinjiang University, Urumqi, Xinjiang 830046, China; School of Environment, Tsinghua University, Beijing 100084, ChinaKey Laboratory of Solid State Physics and Devices Autonomous Region, School of Physics Science and Technology, Xinjiang University, Urumqi 830046, Xinjiang, P. R. China; Key Laboratory of Energy Materials Chemistry, Ministry of Education, Institute of Applied Chemistry, Xinjiang University, Urumqi, Xinjiang 830046, China; School of Environment, Tsinghua University, Beijing 100084, ChinaKey Laboratory of Solid State Physics and Devices Autonomous Region, School of Physics Science and Technology, Xinjiang University, Urumqi 830046, Xinjiang, P. R. China; Key Laboratory of Energy Materials Chemistry, Ministry of Education, Institute of Applied Chemistry, Xinjiang University, Urumqi, Xinjiang 830046, China; School of Environment, Tsinghua University, Beijing 100084, ChinaCorresponding authors.; Key Laboratory of Solid State Physics and Devices Autonomous Region, School of Physics Science and Technology, Xinjiang University, Urumqi 830046, Xinjiang, P. R. China; Key Laboratory of Energy Materials Chemistry, Ministry of Education, Institute of Applied Chemistry, Xinjiang University, Urumqi, Xinjiang 830046, China; School of Environment, Tsinghua University, Beijing 100084, ChinaKey Laboratory of Solid State Physics and Devices Autonomous Region, School of Physics Science and Technology, Xinjiang University, Urumqi 830046, Xinjiang, P. R. China; Key Laboratory of Energy Materials Chemistry, Ministry of Education, Institute of Applied Chemistry, Xinjiang University, Urumqi, Xinjiang 830046, China; School of Environment, Tsinghua University, Beijing 100084, ChinaKey Laboratory of Solid State Physics and Devices Autonomous Region, School of Physics Science and Technology, Xinjiang University, Urumqi 830046, Xinjiang, P. R. China; Key Laboratory of Energy Materials Chemistry, Ministry of Education, Institute of Applied Chemistry, Xinjiang University, Urumqi, Xinjiang 830046, China; School of Environment, Tsinghua University, Beijing 100084, ChinaKey Laboratory of Solid State Physics and Devices Autonomous Region, School of Physics Science and Technology, Xinjiang University, Urumqi 830046, Xinjiang, P. R. China; Key Laboratory of Energy Materials Chemistry, Ministry of Education, Institute of Applied Chemistry, Xinjiang University, Urumqi, Xinjiang 830046, China; School of Environment, Tsinghua University, Beijing 100084, ChinaCorresponding authors.; Key Laboratory of Solid State Physics and Devices Autonomous Region, School of Physics Science and Technology, Xinjiang University, Urumqi 830046, Xinjiang, P. R. China; Key Laboratory of Energy Materials Chemistry, Ministry of Education, Institute of Applied Chemistry, Xinjiang University, Urumqi, Xinjiang 830046, China; School of Environment, Tsinghua University, Beijing 100084, ChinaThe electrochemical CO2 reduction reaction (CER) to methane (CH4) has received great attention. Here, we proposed an efficient method to facilitate the conversion of CO2-to-CH4 by creating a two-phase interface over urea-modified La2CuO4 catalyst. The most optimized one exhibits the highest selectivity (22%) for CH4 and the best activity (14 mA cm−2) and stability (5 h) at the potential of −1 V vs. reversible hydrogen electrode. The enhanced CER performance can be attributed to the establishment of interfacial effect within the two-phase, which facilitates the reduction of Cu2+ and promotes the active sites concentration.http://www.sciencedirect.com/science/article/pii/S1566736723002388La2CuO4CO2 electroreductionCu+ speciesInterfacial effect |
spellingShingle | Shiya Bian Xuekun Jin Jinxing Mi Fengjuan Chen Li Cai Ziyu Wang Junhua Li Jianjun Chen Synergistic effects of interface and valence state on boosting electrochemical CO2 reduction activity of La2CuO4 Catalysis Communications La2CuO4 CO2 electroreduction Cu+ species Interfacial effect |
title | Synergistic effects of interface and valence state on boosting electrochemical CO2 reduction activity of La2CuO4 |
title_full | Synergistic effects of interface and valence state on boosting electrochemical CO2 reduction activity of La2CuO4 |
title_fullStr | Synergistic effects of interface and valence state on boosting electrochemical CO2 reduction activity of La2CuO4 |
title_full_unstemmed | Synergistic effects of interface and valence state on boosting electrochemical CO2 reduction activity of La2CuO4 |
title_short | Synergistic effects of interface and valence state on boosting electrochemical CO2 reduction activity of La2CuO4 |
title_sort | synergistic effects of interface and valence state on boosting electrochemical co2 reduction activity of la2cuo4 |
topic | La2CuO4 CO2 electroreduction Cu+ species Interfacial effect |
url | http://www.sciencedirect.com/science/article/pii/S1566736723002388 |
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