Crystal phase regulation of MnO2 for alcohol oxidation with ultra-stability in acidic solution
The stability of non-noble metal catalysts for water oxidation is remaining a great challenge in acidic solution. Herein, alcohols oxidation instead of water oxidation coupled with ultradurable H2 production was realized. The MnO2 crystal phase regulation could optimize the electronic structure, and...
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Published in | Catalysis communications Vol. 178; p. 106675 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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01.05.2023
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Abstract | The stability of non-noble metal catalysts for water oxidation is remaining a great challenge in acidic solution. Herein, alcohols oxidation instead of water oxidation coupled with ultradurable H2 production was realized. The MnO2 crystal phase regulation could optimize the electronic structure, and the δ-MnO2 with more Mn3+ showed a higher activity, including a low overpotential of 1.48 V at 50 mA cm−2, and a small Tafel slope of 176.22 mV dec−1. Moreover, the δ-MnO2 catalyst exhibited extremely high stability after 24 h for EG oxidation, while the activity was quickly lost within 0.5 h for water oxidation. This work indicated that crystal phase regulation could improve the active and stability of acidic water splitting catalysts.
•Acidic OER replaced by alcohol oxidation greatly enhanced the catalysts stability.•The proportion of Mn3+ in δ-MnO2 could efficiently improve the activity.•The -CH2OH oxidation inhibited the lattice oxygen mechanism.•The crystal phase regulation of MnO2 could optimize the electronic structure. |
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AbstractList | The stability of non-noble metal catalysts for water oxidation is remaining a great challenge in acidic solution. Herein, alcohols oxidation instead of water oxidation coupled with ultradurable H2 production was realized. The MnO2 crystal phase regulation could optimize the electronic structure, and the δ-MnO2 with more Mn3+ showed a higher activity, including a low overpotential of 1.48 V at 50 mA cm−2, and a small Tafel slope of 176.22 mV dec−1. Moreover, the δ-MnO2 catalyst exhibited extremely high stability after 24 h for EG oxidation, while the activity was quickly lost within 0.5 h for water oxidation. This work indicated that crystal phase regulation could improve the active and stability of acidic water splitting catalysts.
•Acidic OER replaced by alcohol oxidation greatly enhanced the catalysts stability.•The proportion of Mn3+ in δ-MnO2 could efficiently improve the activity.•The -CH2OH oxidation inhibited the lattice oxygen mechanism.•The crystal phase regulation of MnO2 could optimize the electronic structure. The stability of non-noble metal catalysts for water oxidation is remaining a great challenge in acidic solution. Herein, alcohols oxidation instead of water oxidation coupled with ultradurable H2 production was realized. The MnO2 crystal phase regulation could optimize the electronic structure, and the δ-MnO2 with more Mn3+ showed a higher activity, including a low overpotential of 1.48 V at 50 mA cm−2, and a small Tafel slope of 176.22 mV dec−1. Moreover, the δ-MnO2 catalyst exhibited extremely high stability after 24 h for EG oxidation, while the activity was quickly lost within 0.5 h for water oxidation. This work indicated that crystal phase regulation could improve the active and stability of acidic water splitting catalysts. |
ArticleNumber | 106675 |
Author | Wang, Xiaojun Yang, Longfei Guo, Zhiyan Li, Junhua Chen, Dawei Du, Fanglin Miao, Ruping Jiang, Yi |
Author_xml | – sequence: 1 givenname: Junhua surname: Li fullname: Li, Junhua organization: College of Material Science and Engineering, Qingdao University of Science and Technology, Zhengzhou Road 53, Qingdao 266042, PR China – sequence: 2 givenname: Xiaojun surname: Wang fullname: Wang, Xiaojun organization: Qingdao Hiworld New Materials Co., Ltd, donghaixi Road 33, Qingdao, 266071, P. R. China – sequence: 3 givenname: Yi surname: Jiang fullname: Jiang, Yi organization: College of Material Science and Engineering, Qingdao University of Science and Technology, Zhengzhou Road 53, Qingdao 266042, PR China – sequence: 4 givenname: Ruping surname: Miao fullname: Miao, Ruping organization: College of Material Science and Engineering, Qingdao University of Science and Technology, Zhengzhou Road 53, Qingdao 266042, PR China – sequence: 5 givenname: Longfei surname: Yang fullname: Yang, Longfei organization: College of Material Science and Engineering, Qingdao University of Science and Technology, Zhengzhou Road 53, Qingdao 266042, PR China – sequence: 6 givenname: Zhiyan surname: Guo fullname: Guo, Zhiyan email: zhiyanguo@qust.edu.cn organization: College of Material Science and Engineering, Qingdao University of Science and Technology, Zhengzhou Road 53, Qingdao 266042, PR China – sequence: 7 givenname: Dawei surname: Chen fullname: Chen, Dawei email: daweichen@qust.edu.cn organization: College of Material Science and Engineering, Qingdao University of Science and Technology, Zhengzhou Road 53, Qingdao 266042, PR China – sequence: 8 givenname: Fanglin surname: Du fullname: Du, Fanglin organization: College of Material Science and Engineering, Qingdao University of Science and Technology, Zhengzhou Road 53, Qingdao 266042, PR China |
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Cites_doi | 10.1016/j.jechem.2022.08.009 10.1039/D1EE03522C 10.1002/anie.202107510 10.1016/j.chempr.2020.07.022 10.1007/s40820-021-00699-z 10.1016/j.electacta.2013.04.007 10.1007/s12274-022-4907-0 10.1002/adma.202003786 10.1021/acscatal.1c01666 10.1039/D1EE01277K 10.1039/C9TA03879E 10.1002/anie.202015773 10.1021/acs.est.8b03696 10.1016/j.jallcom.2020.156625 10.1016/j.cclet.2021.09.076 10.1021/jacs.0c01135 10.1021/acscatal.8b02203 10.1039/C7SC01239J |
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