High Rate Hybrid MnO2@CNT Fabric Anode for Li-Ion Batteries: Properties and Lithium Storage Mechanism by In-Situ Synchrotron X-Ray Scattering

TL;DR

This paper presents a hybrid MnO2@CNT fabric anode with high capacity, stability, and detailed lithium storage mechanisms elucidated through in-situ synchrotron X-ray scattering, advancing Li-ion battery performance.

Contribution

The study introduces a novel MnO2@CNT hybrid anode with exceptional electrochemical performance and provides in-depth mechanistic insights using advanced in-situ characterization techniques.

Findings

Achieved over 1100 mAh/g capacity at 25 mA/g

Maintained 97% capacity after 1500 cycles at 5 A/g

Identified lithium storage mechanisms including intercalation and pseudocapacitance

Abstract

High-performance anodes for rechargeable Li-ion battery are produced by nanostructuring of the transition metal oxides on a conductive support. Here, we demonstrate a hybrid material of MnO2 directly grown onto fabrics of carbon nanotube fibres, which exhibits notable specific capacity over 1100 and 500 mAh/g at a discharge current density of 25 mA/g and 5 A/g, respectively, with coulombic efficiency of 97.5 %. Combined with 97 % capacity retention after 1500 cycles at a current density of 5 A/g, both capacity and stability are significantly above literature data. Detailed investigations involving electrochemical and in situ synchrotron X-ray scattering study reveal that during galvanostatic cycling, MnO2 undergoes an irreversible phase transition to LiMnO2, which stores lithium through an intercalation process, followed by conversion mechanism and pseudocapacitive processes. This mechanism is further confirmed by Raman spectroscopy and X-ray photoelectron spectroscopy. The fraction of pseudocapacitive charge storage ranges from 27% to 83%, for current densities from 25 mA/g to 5 A/g. Firm attachment of the active material to the built-in current collector makes the electrodes flexible and mechanically robust, and ensures that the low charge transfer resistance and the high electrode surface area remain after irreversible phase transition of the active material and extensive cycling.