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Synthesis of a Thiol Building Block for the Crystallization of a Semiconducting Gyroidal Metal-sulfur Framework
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A 2D Covalent Triazine Framework as an Interconvertible Redox Mediator to Promote Sulfur-Conversion Reactions
Chengqiu Li1, Wenkai Zhao2, Hong Yang3
1State Key Laboratory of Explosion Science and Safety Protection, School of Mechatronical Engineering, Beijing Institute of Technology, Beijing, 100081, China.
Abstract:
The sluggish sulfur conversion kinetics have significantly restricted the rate capability and cycling stability of lithium-sulfur (Li-S) batteries. To address this issue, a crystalline pyrene-4, 5, 9, 10-tetraone functionalized covalent triazine framework (CPTO-CTF) is developed, incorporating well-defined nanopores, a fully conjugated framework with abundant redox-active moieties, which can act as an interconvertible and rejuvenated redox mediator to promote sulfur-conversion reactions. The invertible chemical oxidation/reduction between PTO/lithiated PTO and sulfur species can facilitate the conversion reactions and lead to a high utilization of active materials. As a consequence, the CPTO-CTF@S battery delivers high discharge capacity of 1233 mAh g-1 at 0.2 C, high-rate capacity of 604 mAh g-1 at 5 C, and remarkable retention of 95.6% over 600 cycles. The integrated chemical- and electrochemical-pathway further demonstrates its effectiveness in a prototype pouch cell, which delivers a substantial capacity of 810 mAh g-1 at 0.2 C.
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