Manganese MOF-derived ruthenium-doped Mn<sub><i>x</i></sub>O<sub><i>y</i></sub> catalyst for enhanced oxygen evolution reaction and energy-efficient lead recovery

Advanced, efficient, and eco-friendly technologies are essential for the safe recycling of spent lead-acid batteries for minimizing their environmental impact by mitigating toxic wastes and promoting resource sustainability by recovering valuable lead. Herein, we proposed a simple, zero-emission electrochemical strategy to recover metallic lead <i>via</i> the direct electrolysis of lead-acid batteries. Mn<sub><i>x</i></sub>O<sub><i>y</i></sub>@RuO<sub>2</sub> with a layered structure of stacked nanosheets was prepared <i>via</i> facile hydrothermal and annealing methods. Mn<sub><i>x</i></sub>O<sub><i>y</i></sub>@RuO<sub>2</sub> exhibited low overpotentials of 175 mV and 248 mV at a current density of 10 mA cm<sup>-2</sup> in 0.5 mol L<sup>-1</sup> H<sub>2</sub>SO<sub>4</sub> and Pb(MSA)<sub>2</sub>, respectively, showcasing its excellent OER activity. Notably, the catalyst exhibited excellent stability for over 10 hours. The Mn<sub><i>x</i></sub>O<sub><i>y</i></sub>@RuO<sub>2</sub> catalyst during constant current electrolysis required an overpotential of only 375.6 mV at 25 mA cm<sup>-2</sup> to function, greatly reducing the precipitation of PbO<sub>2</sub>. Mn<sub><i>x</i></sub>O<sub><i>y</i></sub>@RuO<sub>2</sub> facilitated high-efficiency oxygen evolution reaction using the lead MSA electrolyte, suppressing the PbO<sub>2</sub> formation and reducing the anode overpotential, making it an ideal anode material for energy-efficient lead recovery.

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Publication Details

Journal
Dalton Transactions
Published
2025-01-01
DOI
https://doi.org/10.1039/d5dt01109d
Citations
1
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
0.36

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Manganese MOF-derived ruthenium-doped MnxOy catalyst for enhanced oxygen evolution reaction and energy-efficient lead recovery

Yanzhi Sun, Jiahong Xie, Pingyu Wan, Junqing Pan et al.
1 citations
Dalton Transactions
Electrocatalysts for Energy Conversion
0.36
article

Manganese MOF-derived ruthenium-doped MnxOy catalyst for enhanced oxygen evolution reaction and energy-efficient lead recovery

Yanzhi Sun, Jiahong Xie, Pingyu Wan, Junqing Pan, Xiaoyue Wang, Wenli Liu, Yongmei Chen, Yang Tang, Rajapriya Andavar
article en
1 citations

Abstract

Advanced, efficient, and eco-friendly technologies are essential for the safe recycling of spent lead-acid batteries for minimizing their environmental impact by mitigating toxic wastes and promoting resource sustainability by recovering valuable lead. Herein, we proposed a simple, zero-emission electrochemical strategy to recover metallic lead <i>via</i> the direct electrolysis of lead-acid batteries. Mn<sub><i>x</i></sub>O<sub><i>y</i></sub>@RuO<sub>2</sub> with a layered structure of stacked nanosheets was prepared <i>via</i> facile hydrothermal and annealing methods. Mn<sub><i>x</i></sub>O<sub><i>y</i></sub>@RuO<sub>2</sub> exhibited low overpotentials of 175 mV and 248 mV at a current density of 10 mA cm<sup>-2</sup> in 0.5 mol L<sup>-1</sup> H<sub>2</sub>SO<sub>4</sub> and Pb(MSA)<sub>2</sub>, respectively, showcasing its excellent OER activity. Notably, the catalyst exhibited excellent stability for over 10 hours. The Mn<sub><i>x</i></sub>O<sub><i>y</i></sub>@RuO<sub>2</sub> catalyst during constant current electrolysis required an overpotential of only 375.6 mV at 25 mA cm<sup>-2</sup> to function, greatly reducing the precipitation of PbO<sub>2</sub>. Mn<sub><i>x</i></sub>O<sub><i>y</i></sub>@RuO<sub>2</sub> facilitated high-efficiency oxygen evolution reaction using the lead MSA electrolyte, suppressing the PbO<sub>2</sub> formation and reducing the anode overpotential, making it an ideal anode material for energy-efficient lead recovery.

Dalton TransactionsVol. 54(30)
Beijing University of Chemical Technology (CN)
National Natural Science Foundation of China
Affordable and clean energy
Openalex Percentile: Top 42%
Electrocatalysts for Energy Conversion
0.36
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