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February 14, 2026Nano Letters3 citations

Fast Iodine Conversion Kinetics Enabled by Highly Electrocatalytic Molybdenum Carbide Nanocrystal-Embedded Ordered Carbon Nanocages

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YZYiming ZhangMHMan HeYZYushuang Zheng

Key Points

  • This research aims to enhance iodine conversion kinetics in zinc-iodine batteries using a novel electrocatalyst.
  • Developed molybdenum carbide nanocrystals within ordered carbon nanocages as an electrocatalyst.
  • Validated the performance through theoretical simulations and in situ Raman spectroscopy.
  • Assessed the battery performance including rate capability and long-term stability under various conditions.
  • Achieved a rate capability of 142 mAh g-1 at 50 C in Zn-I2 batteries with the MoC-OCNCs.
  • Demonstrated good long-term stability and performance with high iodine loadings and pouch-cell configurations.
  • Showed strong polyiodide adsorption and reduced energy barriers for iodine redox reactions.

Abstract

Aqueous zinc-iodine (Zn-I2) batteries are promising for large-scale energy storage but suffer from sluggish redox kinetics and polyiodide shuttling. Herein, molybdenum carbide nanocrystals embedded within ordered carbon nanocages (MoC-OCNCs) are developed as a highly efficient electrocatalyst. The MoC nanocrystals exhibit strong polyiodide adsorption and significantly reduced energy barriers for iodine redox reactions, as validated by theoretical simulations and in situ Raman spectroscopy. Simultaneously, the interconnected hollow OCNC framework ensures rapid electrolyte penetration and efficient mass transport, while acting as a physical barrier to polyiodide diffusion. Consequently, Zn-I2 batteries with the MoC-OCNCs electrocatalyst deliver an impressive rate capability (142 mAh g-1 at 50 C) and good long-term stability. This performance extends to batteries with high iodine loadings and pouch-cell configurations. This work demonstrates that the synergistic integration of highly active nanocrystals within a conductive, porous matrix is critical for accelerating polyiodide conversions in high-performance Zn-I2 systems.

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Cite This Study

Zhang et al. (2026) studied this question.

synapsesocial.com/papers/699011a12ccff479cfe5881dhttps://doi.org/10.1021/acs.nanolett.5c05860
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1In‐Situ Interfacial Reconstruction in Activated Porous Carbon for Dual‐Mechanism Polyiodide Anchoring and Catalytic Conversion in Long‐Life Zinc‐Iodine Batteries2026
  2. 2Synergistic Anion-Mediated Conversion and Single-Atom Catalysis Enable Fast and Reversible Iodine Redox Kinetics2026
  3. 3Catalysis–Deposition Synergistic Strategy to Boost Iodine Redox Kinetics for High-Performance Zinc–Iodine Batteries2026
  4. 4Synergistic Strategy of Catalytic Anchoring and Physical Confinement in a Self‐Supporting Iodine Composite Cathode for Stable Zn‐I <sub>2</sub> Batteries2026
  5. 5Engineering Bifunctional Carbon Hosts with Rich ─OH and ─C═O for Synergistic Confinement and Redox Kinetics in Zn‐I <sub>2</sub> Batteries2026