Ultrathin two-dimensional nanosheet metal-organic frameworks with high-density ligand active sites for advanced lithium-ion capacitors

Two-dimensional (2D) metal-organic frameworks (MOFs) exhibit great promise as high-energy anode materials for next-generation lithium-ion capacitors (LICs) due to their tunable chemistry and short ion transport paths. Nevertheless, high-throughput production of ultrathin 2D MOFs and energy storage mechanism analysis are still full of challenges. Here, theoretical calculations indicate that partial introduction of Fe in Co sites can enhance interaction of metal centers with water in solvents due to the strong 3d-2p orbital binding energy, which induces ultrathin nanosheets, resulting in exposure of high-density ligand active sites, lower band gap and higher Young modulus during lithium insertion. Greatly, ultrathin 2D Co/Fe-BDC nanosheets are obtained with a bottom-up method and can be scaled up to high-throughput production. In/ex-situ results further reveal highly reversible insertion/extraction reactions accompanied by crystalline to amorphous for Co/Fe-BDC anodes. LICs with optimal Co4Fe-BDC anode deliver high energy density (199.7 Wh kg-1) and power density (10,000 W kg-1), together with superior cycle lifespan. This work offers in-depth insights for the high-throughput synthesis and the storage mechanism in 2D MOFs.

Automated summary

Two-dimensional metal-organic frameworks (MOFs) show promise as high-energy anode materials for next-generation lithium-ion capacitors (LICs) due to their tunability and short ion transport paths. This study investigates the production of ultrathin 2D Co/Fe-BDC nanosheets and their storage mechanism. The results demonstrate that LICs with optimal Co4Fe-BDC anodes exhibit high energy density, power density, and superior cycle lifespan.