Shuangwu Xu, Chunlin Xie, Ruotong Wang, Huapeng Sun, Dan Sun, Xianghui Meng, Hongbing Zhang, Linna Che, Yougen Tang, Haiyan Wang
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引用次数: 0
Abstract
Solid‐state sodium batteries (SSSBs) face critical challenges related to interfacial instability and dendritic growth at the interfaces between the sodium metal anode and solid‐state electrolyte (SSE). In this work, a composite anode incorporating a dispersed sodophilic Na2In phase is synthesized by melting a mixture of 5 wt% indium and 95 wt% sodium at 180 °C. This bulk phase reconstruction strategy introduces a large number of sodophilic sites both on the surface and inside the sodium anode, which can durably improve the sodium dendrites, contact voids, and charge localization at the interface between the SSE and the anode. Ultimately, the Na3Zr2Si2PO12‐based symmetric cells assembled with reconstructed sodium‐metal anodes can be cycled for more than 1000 h at a current density of 0.3 mA cm−2, which is much higher than the 10 h of commercial sodium‐metal anodes. SSSBs assembled with a Na3V2(PO4)3 cathode exhibit a capacity retention of 89% after 2000 cycles at a 2 C rate. Importantly, the proposed anode reconstruction strategy—which employs a uniformly distributed sodophilic phase to simultaneously mitigate interfacial contact loss and inhibit dendrite formation—establishes a promising pathway toward practical SSSBs.
固态钠电池(SSSBs)面临着与金属钠阳极和固态电解质(SSE)界面不稳定性和枝晶生长有关的关键挑战。在这项工作中,通过在180°C下熔化5wt %的铟和95wt %的钠的混合物,合成了一种含有分散的亲钠Na2In相的复合阳极。这种体相重构策略在钠阳极表面和内部引入了大量的亲钠位点,可以持久地改善SSE与阳极界面处的钠枝晶、接触空隙和电荷局部化。最终,用重构的金属钠阳极组装的Na3Zr2Si2PO12基对称电池可以在0.3 mA cm - 2的电流密度下循环1000小时以上,这远远高于商用金属钠阳极的10小时。用Na3V2(PO4)3阴极组装的SSSBs在2℃速率下循环2000次后容量保持率为89%。重要的是,所提出的阳极重建策略——采用均匀分布的亲钠相来同时减轻界面接触损失和抑制枝晶的形成——为实际的SSSBs建立了一条有希望的途径。
期刊介绍:
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