Niobates with shear ReO3 crystal structures are remarkably promising anode materials for Li+ batteries due to their large capacities, inherent safety, and high cycling stability. However, they generally suffer from limited rate capabilities rooted in ...
Niobates with shear ReO3 crystal structures are remarkably promising anode materials for Li+ batteries due to their large capacities, inherent safety, and high cycling stability. However, they generally suffer from limited rate capabilities rooted in their insufficient electronic and Li+ conductivities. Here, micrometer‐sized copper niobate (Cu2Nb34O87) bulk as a new anode material having a high electronic conductivity of 2.1 × 10−5 S cm−1 and an impressive average Li+ diffusion coefficient of ≈3.5 × 10−13 cm2 s−1 is exploited, which synergistically leads to an excellent rate capability (184 mAh g−1 at 10 C) while remaining a large reversible capacity and superior cycling stability. Moreover, the fast Li+ transport pathways of grain boundary (micrometer scale) → lattice deformation area (nanometer scale) → (010) crystallographic plane (angstrom scale) are demonstrated in Cu2Nb34O87. Therefore, these results could pave the way for practical application of Cu2Nb34O87 in high‐performance Li+ batteries.
Microsized Copper Niobate having a high electronic conductivity and an impressive average Li+ diffusion coefficient is fabricated via a conventional solid‐state reaction, which exhibits superior electrochemical performance as an anode material. Research on the Li+ transport reveals the fast Li+ transport pathways of the grain boundary (micrometer scale) → lattice deformation area (nanometer scale) → (010) crystallographic plane (angstrom scale).