4.7 Article

Tailoring covalent triazine frameworks anode for superior Lithium-ion storage via thioether engineering

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 469, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2023.143941

Keywords

Covalent triazine frameworks; Thioether groups; Li -ion storage; Li -ion capacitors; Organic anode

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This study designs and synthesizes two tailor-made thioether-functionalized covalent triazine frameworks (S-CTF-Et and S-CTF-Me) as anodes for high-performance lithium-ion capacitors (LICs). The S-CTF-Et anode exhibits a very large reversible capacity, good rate capability, and cycling stability. The lithium-storage mechanism involves multi-electron redox reactions of benzene and triazine rings, and coordination of thioether-groups by the accommodation of Li+. An all CTF-related LIC device assembled with S-CTF-Et anode and CTF-derived porous carbon cathode delivers competitive energy and power densities, and a high capacity retention after a large number of cycles.
The development of high-performance lithium-ion capacitors (LICs) requires the use of electrode materials with higher energy/power density, faster charging, and longer cycle-life. Herein, by taking the merit of the strong designability of covalent triazine frameworks (CTFs), two tailor-made thioether-functionalized CTFs (S-CTF-Et and S-CTF-Me) with tunable properties are designed and synthesized as anodes for LICs. Due to the rich redox active sites and highly accessible specific surface area of the S-CTF-Et anode, which delivers a very large reversible capacity up to 1334 mAh g- 1 at 0.1 A g- 1, good rate capability (520 mAh g- 1 at 2 A g- 1) and cycling stability. After being comprehensively studied via ex-situ FT-IR, ex-situ XPS analyses, and theoretical calculations, it is found that the lithium-storage mechanism involves multi-electron redox reactions of benzene and triazine rings and coordination of thioether-groups by the accommodation of Li+. As proof of the new concept, an all CTFrelated LIC device is assembled with S-CTF-Et anode and CTF-derived porous carbon (CTF-800) cathode for the first time, which delivers competitive energy and power densities (179.3 Wh kg- 1 and 10.7 kW kg- 1) and a capacity retention of 81 % after 10 000 cycles at a large current density of 2 A g- 1.

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