Boosting Structural Reversibility of Na3V2(PO4)3 Cathode via Ti-Cr-Al Synergistic Substitution: From Two-Phase to Quasi-Solid-Solution Reaction in Aqueous Sodium-Ion Storage.
Aug 2026· ACS Applied Materials and Interfaces· 0 citations· 47 references
Medicine
Abstract
Aqueous sodium-ion batteries (ASIBs) are considered promising candidates for large-scale energy storage due to the natural abundance and low cost of sodium. However, the practical application of NASICON-type Na3V2(PO4)3 (NVP) cathodes in aqueous electrolytes is severely hindered by structural degradation and material dissolution, leading to rapid capacity fading. Herein, we propose a multi-metal substitution strategy to address these challenges by successfully synthesizing a Ti, Cr, and Al co-substituted Na3V1Ti1/3Cr1/3Al1/3(PO4)3 (NVTCAP) cathode material via a sol-gel method. The synergistic effect of the incorporated metal ions optimally tunes the crystal lattice, enhancing structural stability and mitigating volume expansion during cycling. This multi-metal substitution effectively suppresses active material dissolution, as revealed by in-situ X-ray diffraction (XRD), and enables the structural evolution of crystals during charging and discharging to exhibit the characteristics of quasi-solid-solution reactions. Quantitatively, the NVTCAP electrode undergoes a continuous structural evolution during Na+ extraction/insertion, with the unit cell volume recovering to within just 0.31% of its initial value after a full cycle. Consequently, the optimized NVTCAP electrode exhibits significantly improved electrochemical kinetics, delivering a high reversible capacity, outstanding rate capability (retaining 86.7% of its initial capacity from 0.1 to 5 A g-1), and exceptional long-term cycling stability (88.6% capacity retention after 3000 cycles at 5 A g-1). When coupled with an activated carbon anode, the NVTCAP cathode maintains superior performance, with 62.1% capacity retention after 5000 cycles. This work demonstrates that multi-metal synergistic substitution is a highly effective strategy for developing high-performance NVP-based cathodes, paving the way for advanced ASIBs with enhanced durability and rate capability.
Na4Fe3(PO4)2P2O7 (NFPP), an iron-based mixed phosphate–pyrophosphate cathode material, has emerged as one of the most commercially promising candidates for large-scale sodium-ion battery (SIB) energy storage applications. Its exceptional characteristics—an ultralow volume change of less than 4% during Na+ de/intercalat...
Na4Fe3(PO4)2P2O7 (NFPP) is regarded as a highly promising cathode material for sodium-ion batteries (SIBs) in energy storage systems. In particular, the low cost and environmental friendliness of NFPP render it especially suitable for large-scale commercialization. Nevertheless, the inherently low ionic/electronic co...
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Na4Co3(PO4)2P2O7 is a representative mixed polyanionic cathode with a high operating voltage and high energy density. However, insufficient cycling stability is the core bottleneck constraining the widespread application of sodium-ion batteries (SIBs). Herein, we propose a synergistic strategy that combines non-stoichi...
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O3-type NaNi0.5Mn0.5O2 is considered a promising cathode material for sodium-ion batteries, but its electrochemical performance is limited by rapid capacity fading associated with Jahn–Teller distortion of Mn3+ and irreversible O3–P3 phase transitions at high voltages. To address these issues, a combined strategy inv...
Na Super Ionic Conductor (NASICON-type) Na3V2(PO4)2F3 (NVPF) is widely recognized as a promising cathode material for sodium-ion batteries (SIBs). However, the low intrinsic electronic conductivity, slow sodium-ion diffusion kinetics, and the inevitable formation of Na3V2(PO4)3 (NVP) impurities have hindered its develo...
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Layered transition-metal oxide NaxTMO2 (TM = Ni, Fe, Mn, etc.) for cathodes in sodium-ion batteries (SIBs) has gained significant research focus owing to its outstanding features, including low cost, ease of synthesis, and environmental benignity. However, it still suffers from poor structural stability, sluggish Na+...