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Zero-Dimensional Ordered Sr2CoMoO6-δ Double Perovskite as High-Rate Anion Intercalation Pseudocapacitance.
Anuj Kumar Tomar1, Akanksha Joshi1, Shalu Atri1
1Department of Chemistry, University of Delhi, Delhi 110007, India.
We developed a B-site cation-ordered double perovskite, Sr2CoMoO6-δ (DP-SCM), for high-performance energy storage. This material exhibits excellent stability, fast ion diffusion, and high capacitance, enabling a symmetric cell with superior energy density.
Area of Science:
- Materials Science
- Electrochemistry
- Solid-State Chemistry
Background:
- Developing stable electrode materials for redox reactions is crucial for energy storage.
- Double perovskites offer potential for tailored structural and electronic properties.
- B-site cation ordering can enhance structural stability and electrochemical performance.
Purpose of the Study:
- To investigate B-site cation ordering in Sr2CoMoO6-δ (DP-SCM) for improved redox stability.
- To explore the relationship between cation ordering, oxygen mobility, and charge storage mechanisms.
- To evaluate the electrochemical performance of DP-SCM as an electrode material for energy storage devices.
Main Methods:
- Synthesis and characterization of B-site cation-ordered double perovskite Sr2CoMoO6-δ.
- X-ray photoelectron spectroscopy (XPS) and Electron Paramagnetic Resonance (EPR) for oxygen vacancy analysis.
- Electrochemical testing including cyclic voltammetry, galvanostatic charge-discharge, and electrochemical impedance spectroscopy.
- Fabrication and testing of a symmetric cell using DP-SCM electrodes.
Main Results:
- Achieved a favorable rock salt structure (0D arrangement) through B-site cation ordering in DP-SCM.
- High oxygen vacancy content facilitated a high oxygen anion diffusion rate (2.03 × 10⁻¹¹ cm² s⁻¹).
- Exhibited fast charge storage kinetics (ΔEp ≈ 0.013 V@ 1 mV s⁻¹) with excellent cycle life (125% retention over 5000 cycles).
- Demonstrated a high capacitance of 747 F g⁻¹ at 1 A g⁻¹ with 56% rate capability up to 10 A g⁻¹.
- A symmetric cell achieved an energy density of 64 Wh kg⁻¹ at 855 W kg⁻¹ with a 1.4 V operating potential.
Conclusions:
- B-site cation ordering in DP-SCM enhances structural stability and electrochemical performance.
- High oxygen mobility and fast anion intercalation are key to the superior charge storage mechanism.
- DP-SCM is a promising electrode material for high-performance energy storage applications.
- Understanding cation ordering and charge storage mechanisms can guide the design of advanced capacitive materials.
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