Related Experiment Video
Updated: Jul 29, 2026

In Situ Neutron Powder Diffraction Using Custom-made Lithium-ion Batteries
Published on: November 10, 2014
Sustainable ZIF-67/Mo-MXene-Derived Nanoarchitecture Synthesis: An Enhanced Durable Performance of Lithium-Selenium
Sowjanya Vallem1, Seunghyun Song1, Yoonju Oh1
1Department of Physics, Gachon University, Seongnam-si, Gyeonggi-do, 461-701, South Korea.
Abstract:
Selenium-based electrodes have garnered attention for their high electrical conductivity, compatibility with carbonate electrolytes, and volumetric capacity comparable to sulfur electrodes. However, real-time application is hindered by rapid capacity deterioration from the "shuttle effect" of polyselenides and volume fluctuations. To address these challenges, a hybrid Se@ZIF-67/Mo-MXene-derived (Se@Co-NC/Mo2C) nanoarchitecture is developed via an economically viable in situ electrostatic self-assembly of ZIF-67 and Mo2C nanosheets. The catalytic effects and porous framework of Co-NC/Mo2C enhance electrode attributes, promoting superior adsorption and conversion of lithium polyselenides and facile ion/electron transport within the electrode, resulting in stable electrochemical performance. Lithium-selenium batteries (LSeBs) exhibit remarkable characteristics, boasting high specific capacity and exceptional durability. The Se@Co-NC/Mo2C electrode delivers a reversible capacity of 503.5 mAh g-1 at 0.5 C with 98% capacity retention, 100% Coulombic efficiency, and exceptional cyclic durability through 8600 cycles. In sustainability tests at 10C/1C charging/discharging, the Se@Co-NC/Mo2C electrode demonstrates an optimistic and stable capacity of ≈370.6 mAh g-1 with 93% capacity retention at the 3100th cycle in a carbonate-based electrolyte and ≈181.3 mAh g-1 with 92% capacity retention after 5000 cycles in an ether-based electrolyte, indicating exceptional stability for practical rechargeable batteries. This cost-effective and efficient approach holds significant potential for high-performance and durable LSeBs.

