Intramolecular Hydrogen Bond Improved Durability and Kinetics for Zinc-Organic Batteries

分子内氢键改善锌有机电池的耐久性和动力学性能

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Abstract

Organic compounds have the advantages of green sustainability and high designability, but their high solubility leads to poor durability of zinc-organic batteries. Herein, a high-performance quinone-based polymer (H-PNADBQ) material is designed by introducing an intramolecular hydrogen bonding (HB) strategy. The intramolecular HB (C=O⋯N-H) is formed in the reaction of 1,4-benzoquinone and 1,5-naphthalene diamine, which efficiently reduces the H-PNADBQ solubility and enhances its charge transfer in theory. In situ ultraviolet-visible analysis further reveals the insolubility of H-PNADBQ during the electrochemical cycles, enabling high durability at different current densities. Specifically, the H-PNADBQ electrode with high loading (10 mg cm(-2)) performs a long cycling life at 125 mA g(-1) (> 290 cycles). The H-PNADBQ also shows high rate capability (137.1 mAh g(-1) at 25 A g(-1)) due to significantly improved kinetics inducted by intramolecular HB. This work provides an efficient approach toward insoluble organic electrode materials.

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