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Updated: Oct 11, 2025

Characterization of Electrode Materials for Lithium Ion and Sodium Ion Batteries Using Synchrotron Radiation Techniques
Published on: November 11, 2013
Mildly Oxidized MXene (Ti3C2, Nb2C, and V2C) Electrocatalyst via a Generic Strategy Enables Longevous Li-O2 Battery
Yongxiang Jiang1, Meng Tian1, Haibo Wang1
1College of Energy, Soochow Institute for Energy and Materials InnovationS (SIEMIS), Key Laboratory of Advanced Carbon Materials and Wearable Energy Technologies of Jiangsu Province, Soochow University, Suzhou 215006, People's Republic of China.
Abstract:
Lithium-oxygen batteries (LOBs) with ultrahigh theoretical energy density have emerged as one appealing candidate for next-generation energy storage devices. Unfortunately, some fundamental issues remain unsettled, involving large overpotential and inferior rate capability, mainly induced by the sluggish reaction kinetics and parasitic reactions at the cathode. Hence, the pursuit of suitable catalyst capable of efficiently catalyzing the oxygen redox reaction and eliminating the side-product generation, become urgent for the development of LOBs. Here, we report a universal synthesis approach to fabricate a suite of mildly oxidized MXenes (mo-Nb2CT, mo-Ti3C2T, and mo-V2CT) as cathode catalysts for LOBs. The readily prepared mo-MXenes possess expanded interlayer distance to accommodate massive Li2O2 formation, and in-situ-formed light metal oxide to enhance the electrocatalytic activity of MXenes. Taken together, the mo-V2CT manages to deliver a high specific capacity of 22752 mAh g-1 at a current density of 100 mA g-1, and a long lifespan of 100 cycles at 500 mA g-1. More impressively, LOBs with mo-V2CT can continuously operate for 90, 89, and 70 cycles, respectively, under a high current density of 1000, 2000, and 3000 mA g-1 with a cutoff capacity of 1000 mAh g-1. The theoretical calculations further reveal the underlying mechanism lies in the optimized surface, where the overpotentials for the formation/decomposition of Li2O2 are significantly reduced and the catalytic kinetics is accelerated. This contribution offers a feasible strategy to prepare MXenes as efficient and robust electrocatalyst toward advanced LOBs and other energy storage devices.
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