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Updated: May 8, 2026

Characterization of Electrode Materials for Lithium Ion and Sodium Ion Batteries Using Synchrotron Radiation Techniques
Published on: November 11, 2013
Polyaniline and alkali cations co-intercalated V2O5 composites with a tremelliform nanosheet structure for high
Zhou Su1, Yishu Yang1, Mingshu Zhao1
1School of Physics, Key Laboratory of Shaanxi for Advanced Functional Materials and Mesoscopic Physics, MOE Key Laboratory for Nonequilibrium Synthesis and Modulation of Condensed Matter, Xi'an Jiaotong University, Xi'an 710049, Shaanxi, China. zhaomshu@mail.xjtu.edu.cn.
Abstract:
Aqueous zinc-ion batteries (AZIBs) have drawn great attention owing to the high intrinsic safety, high power density and numerous advantages of the zinc metal anode. As a cathode material for AZIBs, vanadium pentoxide has a high theoretical capacity of 589 mA h g-1, but it suffers from sluggish Zn2+ diffusion kinetics and rapid capacity degradation. Herein, a co-intercalation strategy of polyaniline (PANI) and alkali cations (Li+, Na+, and K+) is employed to enhance the Zn2+ storage capability of vanadium oxides. As control groups, the sample with only PANI intercalation and the sample without PANI and alkali cation intercalation are synthesized. The evolution of the phase, interlayer distance, morphology and structure for the five samples is investigated. Compared with the intercalation of only PANI, the co-intercalation of PANI and alkali cations further enlarges the interlayer distance (14.80 Å) and maintains the tremelliform nanosheet structure. This co-intercalation strategy promotes the Zn2+ diffusion kinetics, enhances the stability of the layered structure and improves the electronic conductivity. As a result, the electrochemical performance is significantly improved, showing high capacity (409.2 mA h g-1 at 0.2 A g-1), excellent rate capability (261.8 mA h g-1 at 5 A g-1), and favorable cycling stability (capacity retention of 65.4% after 1200 cycles at 5 A g-1).
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