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 inCatalysis communications Vol. 178; p. 106675
Main Authors Li, Junhua, Wang, Xiaojun, Jiang, Yi, Miao, Ruping, Yang, Longfei, Guo, Zhiyan, Chen, Dawei, Du, Fanglin
Format Journal Article
LanguageEnglish
Published Elsevier B.V 01.05.2023
Elsevier
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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.
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
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Keywords MnO2
Nanoparticles
Surfaces
Oxidation
Hydrogen production
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Snippet The stability of non-noble metal catalysts for water oxidation is remaining a great challenge in acidic solution. Herein, alcohols oxidation instead of water...
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StartPage 106675
SubjectTerms Hydrogen production
MnO2
Nanoparticles
Oxidation
Surfaces
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Title Crystal phase regulation of MnO2 for alcohol oxidation with ultra-stability in acidic solution
URI https://dx.doi.org/10.1016/j.catcom.2023.106675
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