Adv Mater. 2026 Apr 8:e22059. doi: 10.1002/adma.202522059. Online ahead of print.
ABSTRACT
Vanadium oxides have emerged as attractive cathode materials for zinc-based batteries owing to their high theoretical capacity and versatile redox chemistry. Nevertheless, their persistent dissolution in aqueous electrolytes remains a long-standing challenge, hindering real-world implementation. Here, we develop a cation-engineered electrolyte strategy enabled by a data-driven framework that integrates density functional theory (DFT) calculations, discrete wavelet transform (DWT)-based multi-scale analysis, and differential feature extraction, to efficiently screen potential hetero-cations and their combinations with objective statistic quantification, while minimizing trial-and-error experimentation and selection bias. As a proof of concept, the Zn/VOx batteries with the predicted Na+-Mg2+-Zn2+ tri-cation electrolyte (NMZ) achieved exceptional reversibility and record-long cycling stability, sustaining 500 cycles at 0.2 A g-1 (1400 h) and 10,000 cycles at 5 A g-1. The tri-cation electrolyte successfully triggers a potential-driven sequential ion insertion pathway involving Na+, Mg2+, and Zn2+, thereby fundamentally suppressing proton intercalation above 1.3 V and hydrated Zn2+ insertion near 1.0 V (vs Zn2+/Zn). This work not only provides valuable data-driven insights into ion-engineering electrochemistry for regulating insertion stability but also uncovers critical ion-related factors that are frequently overlooked. This approach establishes a reusable and statistically robust framework for guiding research across diverse battery chemistries.
PMID:41948846 | DOI:10.1002/adma.202522059
