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Abstract Lithium–sulfur batteries are promising candidates for next‐generation energy storage devices due to their outstanding theoretical energy density. However, they suffer from low sulfur utilization and poor cyclability, greatly limiting their practical implementation. Herein, we adopted a phosphate‐functionalized zirconium metal–organic framework (Zr‐MOF) as a sulfur host. With their porous structure, remarkable electrochemical stability, and synthetic versatility, Zr‐MOFs present great potential in preventing soluble polysulfides from leaching. Phosphate groups were introduced to the framework post‐synthetically since they have shown a strong affinity towards lithium polysulfides and an ability to facilitate Li ion transport. The successful incorporation of phosphate in MOF‐808 was demonstrated by a series of techniques including infrared spectroscopy, solid‐state nuclear magnetic resonance spectroscopy, and X‐ray pair distribution function analysis. When employed in batteries, phosphate‐functionalized Zr‐MOF (MOF‐808‐PO4) exhibits significantly enhanced sulfur utilization and ion diffusion compared to the parent framework, leading to higher capacity and rate capability. The improved capacity retention and inhibited self‐discharge rate also demonstrate effective polysulfide encapsulation utilizing MOF‐808‐PO4. Furthermore, we explored their potential towards high‐density batteries by examining the cycling performance at various sulfur loadings. Our approach to correlate structure with function using hybrid inorganic–organic materials offers new chemical design strategies for advancing battery materials. 

In this work, we synthesize and study the charge transfer properties of a oligosilyl coordination polymer formed from zirconium clusters. Although the synthesized disordered polymer lacks long range order, spectroscopic and computational evidence suggest that the metal-ligand bond is formed, and the principle crystallographic reflections closely match those simulated from inter-node spacings matching that of the ligand. The porous polymer allows for the incorporation of guest molecules as demonstrated by the intercalation of tetracyanoquinodimethane (TCNQ). Charge transfer is predicted from DFT and experimentally observed by infrared spectroscopy, solid-state 29Si nuclear magnetic spectroscopy, and voltammetry. 

Metal–organic frameworks (MOFs) have been an area of intense research for their high porosity and synthetic tunability, which afford them controllable physical and chemical properties for various applications. In this study, we demonstrate that functionalized MOFs can be used to mitigate the so-called polysulfide shuttle effect in lithium–sulfur batteries, a promising next-generation energy storage device. UiO-66-OH, a zirconium-based MOF with 2-hydroxyterephthalic acid, was functionalized with a phosphorus chloride species that was subsequently used to tether polysulfides. In addition, a molecular chlorophosphorane was synthesized as a model system to elucidate the chemical reactivity of the phosphorus moiety. The functionalized MOFs were then used as a cathode additive in coin cell batteries to inhibit the dissolution of polysulfides in solution. Through this work, we show that the functionalization of MOF with phosphorus enhances polysulfide redox and thereby capacity retention in Li–S batteries. While demonstrated here for polysulfide tethering in batteries, we envision this linker functionalization strategy could be more broadly utilized in separations, sensing, or catalysis applications. 

Despite great promise as next-generation high-capacity energy storage devices, lithium–sulfur batteries still face technical challenges in long-term cyclability. With their porous structures and facile synthesis, metal–organic frameworks (MOFs) are tunable platforms for understanding polysulfide redox and can serve as effective sulfur hosts for lithium–sulfur batteries. This feature article describes our design strategies to tailor MOF properties such as polysulfide affinity, ionic conductivity, and porosity for promoting active material utilization and charge transport efficiency. We also present engineering approaches for implementing MOF-based sulfur cathodes for lithium–sulfur batteries with high volumetric density and under low temperature operation. Our studies provide fundamental insights into sulfur–host interactions and polysulfide electrochemistry in the presence of porous matrices, inspiring future designs of advanced batteries. 

Lithium–sulfur (Li–S) batteries have great potential as next generation energy storage devices. However, the redox chemistry mechanism involves the generation of solubilized lithium polysulfides, which can lead to leaching of the active material and, consequently, passivated electrodes and diminished capacities. Chemical tethering of lithium polysulfides to materials in the sulfur cathode is a promising approach for resolving this issue in Li–S batteries. Borrowing from the field of synthetic chemistry, we utilize maleimide functional groups in a Zr-based metal–organic framework to chemically interact with polysulfides through the Michael Addition reaction. A combination of molecular and solid-state spectroscopies confirms covalent attachment of Li 2 S x to the maleimide functionality. When integrated into Li–S cathodes, the maleimide-functionalized framework exhibits notable performance enhancements over that of the unfunctionalized material, revealing the promise of polysulfide anchors for Li–S battery cycling.