Abstract
As a novel energy storage method, photo-assisted rechargeable batteries offer an effective solution to numerous issues currently plaguing organic lithium-ion batteries. Herein, we propose two donor–acceptor (D–A) structure-based organic bifunctional electrode materials (TPA-PTO and CZ-PTO), which integrates photocatalysis and redox activity. The electropolymerization of D–A conjugated polymer extends π-conjugation, reduces the molecular bandgap, broadens the light absorption spectrum, and improves intramolecular electron transfer. Specifically, the long exciton lifetimes enable efficient photo-exciton charge separation and directional charge transfer. Under light irradiation, the photo-electrodes achieved a capacity of 232 mAh g−1 at 0.2 A g−1, while the impedance decreased by 50%. Furthermore, the photo-assisted cell demonstrates remarkable 55% increased capacity at high current density of 10 A g−1. The exciton transfer dynamic mechanisms of photo-assisted dual-ion batteries were also demonstrated by examining the differential effects of light exposure on anion and cation intercalation.
| Original language | English |
|---|---|
| Journal | Angewandte Chemie - International Edition |
| DOIs | |
| Publication status | Accepted/In press - 2026 |
| Externally published | Yes |
Keywords
- dual-ion chemistry
- D–A cathodes
- in situ electropolymerized
- photo-assisted batteries
- photovoltaic mechanism
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