Functionalized Triazine-Based Small Molecules as Efficient Battery Anode Materials
Leveraging the remarkable structural versatility and chemical robustness of triazine frameworks, we synthesized two novel triazine-based derivatives<b>pOMeAni</b> and <b>pOMe2CN</b>and explored their potential as high-performance anode materials for lithium-ion batteries (LIBs). To investigate the effect of the active material content, electrodes with two different loadings (20 and 40%) were evaluated. The electrochemical performance showed that the triazine-based anodes exhibited a high specific capacity of up to 459 mA h g<sup>-1</sup> at 100 mA g<sup>-1</sup> after 100 cycles with nearly 99% Coulombic efficiency. Interestingly, the triazine-based anodes show excellent rate capability and cycling stability at a high current density of 2000 mA g<sup>-1</sup> up to 2000 cycles with a peak capacity of 445 mA h g<sup>-1</sup>. The high current and long-term operation of the triazine-based anode outperformed the commercial graphite-based anode, emphasizing its potential as an alternative anode of LIBs. Furthermore, the mechanistic and kinetic studies on the triazine-based anode reveal structure/performance relationships that shine light on the structural design of high-performance anode materials. These results not only highlight the immense lithium storage potential of triazine derivatives but also open new avenues for the design of next-generation organic electrode materials in sustainable energy storage systems.
Authors
- Mengmei Yang
- Hung‐Ju Yen (ORCID: https://orcid.org/0000-0002-6316-9124)
- Long‐Li Lai (ORCID: https://orcid.org/0000-0002-2152-0430)
- Yao-Chih Lu
- Febri Baskoro (ORCID: https://orcid.org/0000-0001-8408-6726)
Institutions
- Bandung Institute of Technology (ID)
- National Chi Nan University (TW)
- Institute of Chemistry, Academia Sinica (TW)
Publication Details
- Journal
- ACS Omega
- Published
- 2025-09-16
- DOI
- https://doi.org/10.1021/acsomega.5c04787
- Primary Topic
- Advancements in Battery Materials
- Type
- article
- Field-Weighted Citation Impact
- 0.00