Li<sup>+</sup> Diffusion in Li<sub>n</sub>CoNb<sub>2</sub>O<sub>6</sub> (0 &lt; n ≤ 6) Anode with High Capacity Density: Fast Kinetics and Mechanistic Insights

Authors: Yimo Xiang, Shaowen Tan, Jingxian Yu, Shengping Wang

Published: 2025-03-20

DOI: 10.1002/advs.202416001

Source: Full article


Abstract

AbstractThe potential of high power/capacity density and Li+ solid diffusion mechanisms of niobium‐based binary metal oxide (CoNb2O6) anode material are investigated by combining high‐rate Nb2O5 with the redox‐active 3d transition metal Co. CoNb2O6 exhibited exceptional rate capability and cycling stability, which is attributed to anisotropic expansion during cycling and dual diffusion mechanisms at high and low lithium concentrations. The anisotropic expansion of crystals ensures structural stability, whereas the organic combination of a direct‐hopping diffusion mechanism in LinCoNb2O6 (0 ≤ n ≤ 3) and a knock‐off diffusion mechanism in LinCoNb2O6 (3 < n ≤ 6) based on the nudged elastic band (NEB) calculations reveals rapid Li+ solid diffusion and excellent rate performance during lithiation/delithiation. The electrochemical performance of CoNb2O6 also depends on its morphology, where different structures modulate synergistic Nb and Co interactions, influencing Li+ diffusion in the Nb layers. Specifically, the micron‐scale structure formed by secondary particle attachment (CoNb2O6‐MP) provides space for anisotropic expansion, fully utilizing the dual ion diffusion mechanism, enhancing diffusion efficiency, and delivering both high‐capacity density and excellent rate performance. This work not only introduces CoNb2O6 with superior electrochemical properties but also provides insights into the solid diffusion mechanisms under various lithium concentrations, offering a foundation for designing electrode materials with enhanced ion diffusion pathways.