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Defect-rich bimetallic yolk-shell metal-cyanide frameworks as efficient electrocatalysts for oxygen evolution reactions
The rational design and construction of noble-metal-free electrocatalysts with high activity and robust durability for oxygen evolution reactions (OERs) have aroused immense interest in the past decades, but challenges remain. Herein, a reduction-induced dissolution-recrystallization (RIDR) strategy...
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Published in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2021-02, Vol.9 (4), p.2135-2144 |
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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: | The rational design and construction of noble-metal-free electrocatalysts with high activity and robust durability for oxygen evolution reactions (OERs) have aroused immense interest in the past decades, but challenges remain. Herein, a reduction-induced dissolution-recrystallization (RIDR) strategy was developed to fabricate a defect-rich yolk-shell Prussian-blue analogue (YS-PBA) by a solvothermal process in isopropyl alcohol (IPA) in the presence of polyvinylpyrrolidone (PVP). The experimental result indicated that the defect-rich YS-PBA was formed
via
phase transformation from Co
3
[Fe
III
(CN)
6
]
2
to Co
2
Fe
II
(CN)
6
induced by the reduction potential of the IPA-PVP couple. The newly synthesized YS-PBA exhibited outstanding OER performance with a low overpotential of 293 mV to deliver a current density of 10 mA cm
−2
and long-term durability (120 h) in alkaline media. Both experimental and density functional theory (DFT) results unveiled that the defects formed in YS-PBA cause a dramatic positive effect on the improvement of the OER activity.
A defect-rich yolk-shell Co-Fe Prussian-blue analogue was fabricated using a reduction-induced dissolution-recrystallization strategy, which exhibited enhanced OER performance in an alkaline medium. |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/d0ta09892b |