By enabling fast Zn²⁺ transport and durable cycling, the DNA‑engineered MnO₂ cathode tackles the rate‑performance and lifespan constraints that have hindered commercial uptake of aqueous zinc‑ion batteries.
Aqueous zinc‑ion batteries are gaining attention as low‑cost, intrinsically safe alternatives to lithium‑based systems, yet their commercial viability hinges on cathode materials that can sustain rapid ion transport without degrading. Manganese dioxide, with its high theoretical capacity and environmental friendliness, is a leading candidate, but conventional synthesis often yields densely stacked crystals that collapse under high‑rate cycling, limiting power density and cycle life.
The DNA‑assisted hydrothermal method introduces a green, biomolecular templating strategy where deoxyribonucleic acid supplies phosphate and nitrogen functionalities that chelate Mn ions during nucleation. This coordination produces loosely stacked δ‑MnO₂ nanoflakes enriched with oxygen‑related defects and a higher Mn³⁺ fraction, subtly expanding the interlayer spacing. The resulting porous architecture offers abundant active sites and short diffusion pathways, dramatically accelerating Zn²⁺ insertion/extraction while preserving structural integrity.
Performance testing shows the DNA‑engineered cathode achieving 293.3 mAh g⁻¹ at a modest 0.2 A g⁻¹ and maintaining 121.6 mAh g⁻¹ at an aggressive 10 A g⁻¹, alongside 86.5 % capacity retention after 500 cycles and 53.8 mAh g⁻¹ after 10 000 cycles. These metrics surpass many reported MnO₂ systems, positioning the material as a viable high‑power, long‑life solution for grid‑scale storage. Moreover, the use of DNA as a sustainable structure‑directing agent aligns with circular‑economy goals, suggesting a pathway toward scalable, eco‑friendly manufacturing of next‑generation zinc‑ion batteries.
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