Abstract
Organic redox flow batteries operating in alkaline media have attracted significant attention for their inherent safety and environmental compatibility. However, conventional quinone- and ketone-based anolytes suffer from low electron-transfer numbers (≤2 e− per molecule), irreversible isomerization and concentration-dependent side reactions, ultimately limiting their energy density and long-term cycling stability. Here, we introduce a molecular engineering strategy that leverages the conjugation of heterogeneous redox centers to fuse distinct redox-active motifs, thereby creating a new composite phenazine-ketone molecule capable of a six-electron transfer process. This multi-hetero-redox center fused scaffold not only overcomes the intrinsic limitations of conventional structures but also exhibits robust kinetics and chemical stability in an alkaline electrolyte. The resulting compound delivers a record capacity of 79.3 Ah L−1, and sustains stable operation over 3500 cycles (198.5 days), offering a viable pathway toward next-generation high-energy-density, durable and sustainable energy storage technologies.
| Original language | English |
|---|---|
| Article number | nwag423 |
| Journal | National Science Review |
| Volume | 13 |
| Issue number | 16 |
| DOIs | |
| State | Published - Aug 2026 |
Keywords
- anolyte
- hetero-redox center conjugation
- high energy density
- multi-electron transfer
- redox flow battery
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