Abstract

Prussian blue analogues (PBAs) are promising anode materials for lithium-ion batteries due to the unique 3D open frameworks, but inferior cycling performance and poor rate capability restrict their application. Herein, Co-Fe PBA@honeycomb carbon is prepared by means of well-designed solution evaporation assembly and in-situ etching-coordination strategy. K0.90Co[Fe(CN)6]0.97□0.03⋅0·.44H2O (□: vacancy defect) cubes with uniform size of 20 nm are grown within every honeycomb carbon pore with a diameter of ∼ 180 nm. The mass content of Co-Fe PBA reaches 78.61 wt%. The small size, low defects and less interstitial/coordinated water improve kinetics properties and robustness of Co-Fe PBA. Honeycomb carbon further enhances the electronic conductivity and structural stability of Co-Fe PBA. Accordingly, Co-Fe PBA@honeycomb carbon exhibits high reversible capacities of 915 mAh/g at 0.5 A/g after 200 cycles, 658 mAh/g at 1 A/g after 1000 cycles, 496 mAh/g at 2 A/g after 450 cycles. Rate performance and kinetics properties are superior. The reversible capacity at 5 A/g is as high as 328 mAh/g. The diffusion coefficient of Li+ reaches 10−10.0 ∼ 10−11.7 cm2 s−1. Ex-situ scanning electron microscopy and Fourier transform infrared spectrometer demonstrate that the cycled Co-Fe PBA@honeycomb carbon is stable.

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