Cycling Reconstructed Hierarchical Nanoporous High-Entropy Oxides with Continuously Increasing Capacity for Li Storage

High-entropy oxides (HEOs) have been showing great promise in a wide range of applications. There remains a lack of clarity regarding the influence of nanostructure and composition on their Li storage performance. Herein, a dealloying technique to synthesize hierarchical nanoporous HEOs with tunable compositions is employed. Building upon the extensively studied quinary AlFeNiCrMnOx, an additional element (Co, V, Ti, or Cu) is introduced to create senary HEOs, allowing for investigation of the impact of the added component on Li storage performance. With higher specific surface areas and oxygen vacancy concentrations, all their HEOs exhibit high Li storage performances. Remarkably, the senary HEO with the addition of V (AlNiFeCrMnVOx) achieves an impressive capacity of 730.2 mAh g-1 at 2.0 A g-1, which surpasses all reported performance of HEOs. This result demonstrates the synergistic interaction of the six elements in one HEO nanostructure. Additionally, the battery cycling-induced reconstruction and cation diffusion in the HEOs is uncovered, which results in an initial capacity decrease followed by a subsequent continuous capacity increase and enhanced Li ion diffusion. The results highlight the crucial roles played by both nanoporous structure design and composition optimization in enhancing Li storage of HEOs. This work reports the Li storage properties of nanoporous high-entropy spinel oxide. The authors found that the addition of V, Co, or Ti beyond five elements can enhance the Li storage performance. Especially, the AlNiFeMnCrV combination delivered the highest capacity of 730.2 mAh g-1 at 2.0 A g-1.image