阴极
材料科学
电化学
阳极
储能
容量损失
限制
化学工程
氧化还原
钠
有机自由基电池
纳米技术
电极
化学
机械工程
物理
工程类
物理化学
功率(物理)
量子力学
冶金
作者
Chinmaya Mirle,P. Schuster,Ludmila Kolb,Litwin Jacob,Alexander J. C. Kuehne
标识
DOI:10.1002/advs.202500484
摘要
Sodium batteries (SBs) are a promising alternative to lithium-ion batteries (LIBs) due to the abundance, cost-effectiveness, and environmental sustainability of sodium. However, the larger ionic radius of Na+ leads to challenges in electrode stability, limiting the performance of conventional inorganic cathode materials. Redox-active organic compounds, particularly π-conjugated quinones, have emerged as a viable alternative, due to their tunable electrochemical properties, structural flexibility, and enhanced compatibility with Na+. Despite their advantages, many quinone-based cathodes suffer from limited cycling stability and solubility issues. Here, the synthesis and characterization of poly(pentacenetetrone) (PPT) as a high-capacity cathode material for SBs is reported. PPT exhibits a high theoretical specific capacity (Qtsp = 319 mAh g⁻¹) and achieves an experimental specific capacity (Qsp) of 314 mAh g⁻¹ at 0.2C, with remarkable cycling stability. At 2C, the capacity remains at 260 mAh g⁻¹, retaining 92% after 500 cycles. PPT demonstrates excellent rate capability with 98% capacity retention after extended cycling. These findings highlight the potential of PPT as a high-performance cathode material for sodium batteries, addressing critical challenges in scalability and long-term stability for next-generation energy storage systems.
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