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.
Authors
- Siwen Zhang (ORCID: https://orcid.org/0000-0002-1706-0400)
- Hongge Pan (ORCID: https://orcid.org/0000-0002-7582-3744)
- Tianyi Ma (ORCID: https://orcid.org/0000-0002-1042-8700)
- Wenhui Mi (ORCID: https://orcid.org/0000-0002-1612-5292)
- Miqiu Kong (ORCID: https://orcid.org/0000-0002-1591-4249)
- Minghui Liu (ORCID: https://orcid.org/0000-0002-1803-2452)
- Hui Li (ORCID: https://orcid.org/0000-0002-0996-2092)
- Zhibiao Wang (ORCID: https://orcid.org/0000-0002-4462-2712)
- Bosi Yin
- Haixi Gu
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
- Field-Weighted Citation Impact
- 0.00