Abstract

Investigating independent active materials is inadequate to settle the technological challenges involved in the booming lithium ion battery industry. The further development of energy-storage properties with both high energy density and superior cycling lifespan are highly dependent on the overall system optimization, which highlights the study of the interface between different components in a system. Herein, a system-level strategy of engineering MnO-based anode build on the plentiful electrolytic manganese dioxide are developed via a microwave-assisted carbothermic reduction, combined with a succeeding in-situ aggregation of polydopamine (PD) onto MnO along with chemical binding with polyacrylic acid (PAA) binder. Fourier transform IR spectra, X-ray photoelectron spectroscopy spectra validate the formation of cross-linking reaction between the PD buffer and PAA binder. Benefited from the prominent structure stability which endowed by well-connected three-dimensional porous structure, as well as two steady interfaces between MnO and PD buffer and between PD buffer and PAA binder, the cross-linked MnO anode exhibit a reversible capacity of 687 mAh g−1 at 300 mA g−1 and high Coulombic efficiency of 99% over 500 cycles and impressive rate capability of 320 mAh g−1 at 3000 mA g−1.

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