Breaking diffusion constraints through fluorine-regulated MnO <sub> <i>x</i> </sub> /KMnF <sub>3</sub> heterostructures for enhanced aqueous Mg <sup>2+</sup> storage

With the continuing demand for clean and sustainable energy storage devices, aqueous magnesium-ion capacitors have gained prominence as a viable electrochemical solution. However, high-performance aqueous magnesium-ion storage devices for energy need to satisfy rigorous requirements due to the large hydrated ionic radius of Mg<sup>2+</sup> cations and the structural collapse of host materials during insertion/extraction. Herein, we propose a fluorine-mediated structural regulation strategy to design multivalent manganese oxides (F-m-MnO<sub>x</sub>) as cathode materials. By partially substituting oxygen sites with fluorine atoms, high-strength Mn-F bonds are formed within the MnO<sub>2</sub> lattice, which locally enhance the framework stability by reinforcing the tunnel structure and effectively suppressing structural degradation during cycling. Furthermore, the robust Mn-F bond energy enables a unique “pinning effect” anchoring hydrothermally synthesized KMnF<sub>3</sub> nanoparticles onto the MnO<sub>2</sub> matrix. These KMnF<sub>3 </sub>nanoparticles act as dynamic bridges during Mg<sup>2+</sup> insertion/extraction processes, with their surface-exposed chemically active sites facilitating transient yet reversible interactions with migrating Mg<sup>2+</sup> ions. This innovative design significantly enhances Mg<sup>2+</sup> diffusion kinetics through the bulk phase, offering a groundbreaking mechanism to overcome the inherent sluggish ion transport in multivalent cation systems. The F-m-MnO<sub>x</sub> cathode delivers exceptional performance metrics: a high specific capacity of 142 mAh/g at 0.1 A/g, outstanding cycling stability (89.6% retention after 1800 cycles), and rapid kinetics. This research not only establishes an innovative design concept for advanced electrode materials through halogen-mediated structural engineering but also elucidates the dual magnesium-ion storage mechanism involving both KMnF<sub>3</sub> and MnO<sub>2</sub> in F-m-MnO<sub>x</sub> through ex-situ characterization, enabling new possibilities for future clean energy storage.

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Publication Details

Journal
Nano Research
Published
2025-09-03
DOI
https://doi.org/10.26599/nr.2025.94908028
Primary Topic
Geochemistry and Elemental Analysis
Type
article
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article

Breaking diffusion constraints through fluorine-regulated MnO x /KMnF 3 heterostructures for enhanced aqueous Mg 2+ storage

Siwen Zhang, Hongge Pan, Tianyi Ma, Wenhui Mi et al.
Nano Research
Geochemistry and Elemental Analysis
article

Breaking diffusion constraints through fluorine-regulated MnO x /KMnF 3 heterostructures for enhanced aqueous Mg 2+ storage

Siwen Zhang, Hongge Pan, Tianyi Ma, Wenhui Mi, Miqiu Kong, Minghui Liu, Hui Li, Zhibiao Wang, Bosi Yin, Haixi Gu
article en

Abstract

With the continuing demand for clean and sustainable energy storage devices, aqueous magnesium-ion capacitors have gained prominence as a viable electrochemical solution. However, high-performance aqueous magnesium-ion storage devices for energy need to satisfy rigorous requirements due to the large hydrated ionic radius of Mg<sup>2+</sup> cations and the structural collapse of host materials during insertion/extraction. Herein, we propose a fluorine-mediated structural regulation strategy to design multivalent manganese oxides (F-m-MnO<sub>x</sub>) as cathode materials. By partially substituting oxygen sites with fluorine atoms, high-strength Mn-F bonds are formed within the MnO<sub>2</sub> lattice, which locally enhance the framework stability by reinforcing the tunnel structure and effectively suppressing structural degradation during cycling. Furthermore, the robust Mn-F bond energy enables a unique “pinning effect” anchoring hydrothermally synthesized KMnF<sub>3</sub> nanoparticles onto the MnO<sub>2</sub> matrix. These KMnF<sub>3 </sub>nanoparticles act as dynamic bridges during Mg<sup>2+</sup> insertion/extraction processes, with their surface-exposed chemically active sites facilitating transient yet reversible interactions with migrating Mg<sup>2+</sup> ions. This innovative design significantly enhances Mg<sup>2+</sup> diffusion kinetics through the bulk phase, offering a groundbreaking mechanism to overcome the inherent sluggish ion transport in multivalent cation systems. The F-m-MnO<sub>x</sub> cathode delivers exceptional performance metrics: a high specific capacity of 142 mAh/g at 0.1 A/g, outstanding cycling stability (89.6% retention after 1800 cycles), and rapid kinetics. This research not only establishes an innovative design concept for advanced electrode materials through halogen-mediated structural engineering but also elucidates the dual magnesium-ion storage mechanism involving both KMnF<sub>3</sub> and MnO<sub>2</sub> in F-m-MnO<sub>x</sub> through ex-situ characterization, enabling new possibilities for future clean energy storage.

Nano ResearchVol. 19(2)
Openalex Percentile: Top 80%
Geochemistry and Elemental Analysis
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