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Manipulating electronic delocalization of Mn3O4 by manganese defects for oxygen reduction reaction
[Display omitted] •Mn-defected Mn3O4 was synthesized by thermal oxidation of manganese glycerate.•Mn defects tune electronic delocalization to improve conductivity.•Mn defects result in more surface Mn3+ as major active site.•O2 activation and OH* desorption are facilitated by Mn defects.•Mn defects...
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Published in: | Applied catalysis. B, Environmental Environmental, 2020-11, Vol.277, p.119247, Article 119247 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | [Display omitted]
•Mn-defected Mn3O4 was synthesized by thermal oxidation of manganese glycerate.•Mn defects tune electronic delocalization to improve conductivity.•Mn defects result in more surface Mn3+ as major active site.•O2 activation and OH* desorption are facilitated by Mn defects.•Mn defects reduce the Gibbs free energy variation in the rate-limiting step.
Manganese-based oxides are promising in electrocatalytic oxygen reduction reaction, but the activity and conductivity need further improvement. Herein manganese defected Mn3O4 was fabricated by solvothermal synthesis of manganese glycerate and then thermal calcination. The experimental and computational results reveal that manganese defects in Mn3O4 modify the electronic structure to improve conductivity and electronic delocalization, which helps to expose more surface Mn3+ as major active site, thereby facilitating O2 activation and OH* desorption, and reducing the Gibbs free energy variation in the rate-limiting step of ORR. Accordingly, the onset potential, half-wave potential and limiting current density of manganese defected Mn3O4 are 0.87 V, 0.65 V and 5.0 mA cm-2, better than that of normal Mn3O4 (0.77 V, 0.62 V and 2.6 mA cm-2). This work provides an effective approach to tune the defects and electronic structures of Mn3O4 for better electrochemical activity. |
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ISSN: | 0926-3373 1873-3883 |
DOI: | 10.1016/j.apcatb.2020.119247 |