News Release

Tellurium‑terminated MXene synthesis via one‑step tellurium etching

Peer-Reviewed Publication

Shanghai Jiao Tong University Journal Center

Tellurium‑Terminated MXene Synthesis via One‑Step Tellurium Etching

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  • A novel and efficient Te etching method for the preparation of Te-functionalized MXene materials is presented
  • This simple etching method enables the processing of V- and Nb-based MAX phases and demonstrates potential for large-scale production.
  • V2CTex MXene has a sodium storage capacity of up to 247 mAh g−1 and maintains 216 mAh g−1 at 23 C.
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Credit: Guoliang Ma, Zongbin Luo, Hui Shao, Yanbin Shen, Zifeng Lin, Patrice Simon.

As demand grows for high-performance sodium-ion batteries, the limits of traditional electrode materials in capacity and rate capability become more evident. Now, researchers from Sichuan University, SINANO-CAS, and Université de Toulouse, led by Prof. Zifeng Lin, Prof. Hui Shao, and Prof. Patrice Simon, have unveiled a breakthrough one-step elemental-tellurium etching strategy to produce Te-terminated MXenes. This work opens a scalable, fluoride-free route to next-generation 2D materials with superior sodium-storage properties.

Why Te-Terminated MXenes Matter

  • Extraordinary Capacity: V2CTex delivers 247 mAh g-1 at 0.05 A g-1 and retains 216 mAh g-1 at a 23 C rate—>50 % higher than conventional Cl-, Br-, or F-terminated MXenes.
  • Long-Life Cycling: >90 % capacity retention after 1 000 cycles at 0.1 A g-1, enabled by stable Na–Te alloying confined on 2D scaffolds.
  • Eco-Friendly & Scalable: Elemental Te etching eliminates toxic HF, operates at 700 °C under Ar, and is demonstrated on 20 g batches with 77 % yield and full Te recyclability.

Innovative Design and Features

  • One-Step Redox Chemistry: Liquid Te selectively removes Al from MAX phases while grafting Te termini in situ, expanding interlayer spacing to 12.6 Å and preserving high electrical conductivity (45 S m-1).
  • Universal MAX Compatibility: Successful etching of Ti-, V-, Nb-, Ta-, Cr-, Zr-based MAX phases (211, 312, 413 types) producing accordion-like MXenes with tunable surface chemistry.
  • Mechanistic Insight: DFT shows strong Te adsorption on Al sites (−2.63 eV) driving Al2Te3 formation; Na preferentially bonds to surface Te vacancies, combining 2D ion channels with chalcogenide alloying for fast, stable storage.

Applications and Future Outlook

  • Sodium-Ion Batteries: Te-MXene anodes exhibit high-rate capability (5 A g-1) and low polarization, enabling full cells with 104 mAh g-1 at 0.1 A g-1.
  • Beyond Na-Ion: The elemental-etching concept (Te/Se/S/P) offers a versatile toolbox to tailor MXene terminations for Li-, K-, Zn-, and multivalent-ion systems.
  • Sustainability: Te is recoverable via electrochemical reduction, positioning the process for closed-loop manufacturing.

This comprehensive study redefines MXene synthesis by merging controllable surface functionalization with green chemistry, delivering electrode materials that push sodium-ion technology toward higher energy and power densities. Stay tuned for more cutting-edge advances from Prof. Lin, Prof. Shao, and Prof. Simon’s teams!


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