Inhibiting irreversible Zn2+/H+ co-insertion chemistry in aqueous zinc-MoO batteries for enhanced capacity stability

A polyaniline strategy is developed to inhibit the irreversible Zn 2+ /H + co-intercalation/extraction process in MoO 3 cathode for aqueous Zn batteries. This innovative approach delivers an unprecedented capacity and prolonged cycling stability. Rechargeable aqueous Zn-MoO x batteries are promising energy storage devices with high theoretical specific capacity and low cost. However, MoO 3 cathodes suffer drastic capacity decay during the initial discharging/charging process in conventional electrolytes, resulting in a short cycle life and challenging the development of Zn-MoO x batteries. Here we comprehensively investigate the dissolution mechanism of MoO 3 cathodes and innovatively introduce a polymer to inhibit the irreversible processes. Our findings reveal that this capacity decay originates from the irreversible Zn 2+ /H + co-intercalation/extraction process in aqueous electrolytes. Even worse, during Zn 2+ intercalation, the formed Zn x MoO 3− x intermediate phase with lower valence states (Mo 5+ /Mo 4+ ) experiences severe dissolution in aqueous environments. To address these challenges, we developed a first instance of coating a polyaniline (PANI) shell around the MoO 3 nanorod effectively inhibiting these irreversible processes and protecting structural integrity during long-term cycling. Detailed structural analysis and theoretical calculations indicate that =N– groups in PANI@MoO 3− x simultaneously weaken H + adsorption and enhance Zn 2+ adsorption, which endowed the PANI@MoO 3− x cathode with reversible Zn 2+ /H + intercalation/extraction. Consequently, the obtained PANI@MoO 3− x cathode delivers an excellent discharge capacity of 316.86 mA h g −1 at 0.1 A g −1 and prolonged cycling stability of 75.49% capacity retention after 1000 cycles at 5 A g −1 . This work addresses the critical issues associated with MoO 3 cathodes and significantly advances the understanding of competitive multi-ion energy storage mechanisms in aqueous Zn-MoO 3 batteries.

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Publication Details

Journal
Journal of Energy Chemistry
Published
2024-11-05
DOI
https://doi.org/10.1016/j.jechem.2024.10.034
Citations
7
Primary Topic
Advanced battery technologies research
Type
article
Field-Weighted Citation Impact
1.46

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article

Inhibiting irreversible Zn2+/H+ co-insertion chemistry in aqueous zinc-MoO batteries for enhanced capacity stability

Xiaoguang Duan, Xu Han, Zihang Huang, Shuai Mao et al.
7 citations
Journal of Energy Chemistry
Advanced battery technologies research
1.46
article

Inhibiting irreversible Zn2+/H+ co-insertion chemistry in aqueous zinc-MoO batteries for enhanced capacity stability

Xiaoguang Duan, Xu Han, Zihang Huang, Shuai Mao, Xinwei Guan, Tianyi Ma, Zheng Chen, Hui Li
article en
7 citations

Abstract

A polyaniline strategy is developed to inhibit the irreversible Zn 2+ /H + co-intercalation/extraction process in MoO 3 cathode for aqueous Zn batteries. This innovative approach delivers an unprecedented capacity and prolonged cycling stability. Rechargeable aqueous Zn-MoO x batteries are promising energy storage devices with high theoretical specific capacity and low cost. However, MoO 3 cathodes suffer drastic capacity decay during the initial discharging/charging process in conventional electrolytes, resulting in a short cycle life and challenging the development of Zn-MoO x batteries. Here we comprehensively investigate the dissolution mechanism of MoO 3 cathodes and innovatively introduce a polymer to inhibit the irreversible processes. Our findings reveal that this capacity decay originates from the irreversible Zn 2+ /H + co-intercalation/extraction process in aqueous electrolytes. Even worse, during Zn 2+ intercalation, the formed Zn x MoO 3− x intermediate phase with lower valence states (Mo 5+ /Mo 4+ ) experiences severe dissolution in aqueous environments. To address these challenges, we developed a first instance of coating a polyaniline (PANI) shell around the MoO 3 nanorod effectively inhibiting these irreversible processes and protecting structural integrity during long-term cycling. Detailed structural analysis and theoretical calculations indicate that =N– groups in PANI@MoO 3− x simultaneously weaken H + adsorption and enhance Zn 2+ adsorption, which endowed the PANI@MoO 3− x cathode with reversible Zn 2+ /H + intercalation/extraction. Consequently, the obtained PANI@MoO 3− x cathode delivers an excellent discharge capacity of 316.86 mA h g −1 at 0.1 A g −1 and prolonged cycling stability of 75.49% capacity retention after 1000 cycles at 5 A g −1 . This work addresses the critical issues associated with MoO 3 cathodes and significantly advances the understanding of competitive multi-ion energy storage mechanisms in aqueous Zn-MoO 3 batteries.

Journal of Energy ChemistryVol. 102
Liaoning University (CN), Ningbo Institute of Industrial Technology (CN), The University of Adelaide (AU), RMIT University (AU)
National Natural Science Foundation of China, Australian Research Council
Affordable and clean energy
Openalex Percentile: Top 17%
Advanced battery technologies research
1.46
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