Bipolar Conjugated Microporous Polymer with Intrinsically Fast Reaction Kinetics for High-Energy-Density and High-Rate-Capacity Symmetric All-Organic Lithium-Ion Battery

Abstract

The development of high-performance symmetric all-organic batteries (SAOBs) is of great significance for next-generation environmentally friendly energy storage systems with high energy and power densities. Herein, we report a bipolar conjugated microporous polymer (CMP), named as PTTA that synthesized by integrating p-type Tris(4-formylphenyl)amine and n-type 2,7-diaminopyrene-4,5,9,10-tetraone. It features with unique donor-acceptor (D−A) structure, hierarchical porosity, abundant redox-active sites, and chemical stability, which collectively endow PTTA with intrinsically fast electrochemical reaction kinetics. As a cathode, PTTA delivers a high specific capacity of 353 and 140 mAh g–1 at 0.1 and 10 A g–1, respectively, with 91% capacity retention after 2000 cycles at 5 A g–1. As an anode, it achieves a high specific capacity of 1789 mAh g–1 at 0.1 A g–1. A PTTA-based SAOB (PTTA/PP/PTTA) in coin cells provides 257 mAh g–1 at 1.0 C and 148 mAh g–1 at 67.9 C. Moreover, a high-loading pouch-type device maintains high electrochemical performance and reaches 277 Wh kg–1. This demonstrates device-level feasibility and highlights the benefits of the D–A molecular design and hierarchical porosity in facilitating efficient bipolar redox reactions and fast charge storage. This work provides a valuable insight into the structure-function design principle of porous polymer for high-performance SAOB electrodes.

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Article information

Article type
Paper
Submitted
26 Jan 2026
Accepted
10 Mar 2026
First published
11 Mar 2026

J. Mater. Chem. A, 2026, Accepted Manuscript

Bipolar Conjugated Microporous Polymer with Intrinsically Fast Reaction Kinetics for High-Energy-Density and High-Rate-Capacity Symmetric All-Organic Lithium-Ion Battery

H. Liu, L. Teng, W. He, X. Zhang, L. Xu, J. Duan, L. Wang, Y. Zhang, B. Sun, Y. Liao and W. Lyu, J. Mater. Chem. A, 2026, Accepted Manuscript , DOI: 10.1039/D6TA00755D

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