Mechanically Robust Bismuth-Embedded Carbon Microspheres for Ultrafast Charging and Ultrastable Sodium-Ion Batteries

IF 14.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Journal of the American Chemical Society Pub Date : 2025-01-14 DOI:10.1021/jacs.4c09824
Jianhai Pan, Zhefei Sun, Xiaoyu Wu, Tongchao Liu, Yurui Xing, Jiawei Chen, Zhichen Xue, Dafu Tang, Xiaoli Dong, Hongti Zhang, Haodong Liu, Qiulong Wei, Dong-Liang Peng, Khalil Amine, Qiaobao Zhang
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Abstract

Advancements in the development of fast-charging and long-lasting microstructured alloying anodes with high volumetric capacities are essential for enhancing the operational efficiency of sodium-ion batteries (SIBs). These anodes, however, face challenges such as declined cyclability and rate capability, primarily due to mechanical degradation reduced by significant volumetric changes (over 252%) and slow kinetics of sodium-ion storage. Herein, we introduce a novel anode design featuring densely packed bismuth (Bi) embedded within highly conductive carbon microspheres to overcome the aforementioned challenges. Remarkably, the high loading Bi anode within carbon microspheres with a high tap density of 2.59 g cm–3 possesses significant mechanical strength exceeding 590 MPa and limits volume swelling of only 10.9% post-sodiation. This anode demonstrates a high volumetric capacity (908.3 mAh cm–3), ultrafast chargeability (200 A g–1, full charge/discharge in just 5.5 s), and outstanding cyclability over 12,000 cycles and maintains exceptional cycling stability even at −30 °C. The full cell paired with a Na3V2(PO4)3 cathode retains over 80% capacity after 600 cycles at 36 C, demonstrating a remarkable rate capability of 126 C (full charge/discharge in 28.6 s). Our comprehensive experimental evaluations and chemo-mechanical simulations shed light on the mechanisms underpinning the anode’s superior performance. This development marks a significant advancement in the design of durable and fast-charging anodes for high-performance SIBs.

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用于超快充电和超稳定钠离子电池的机械坚固铋嵌入碳微球
快速充电和高容量持久微结构合金阳极的发展是提高钠离子电池(sib)运行效率的必要条件。然而,这些阳极面临着诸如可循环性和速率能力下降等挑战,主要是由于显著的体积变化(超过252%)和钠离子储存动力学缓慢而导致的机械降解。在此,我们介绍了一种新的阳极设计,该设计将高密度的铋(Bi)嵌入高导电性碳微球中,以克服上述挑战。值得注意的是,高负载铋阳极在碳微球中具有2.59 g cm-3的高丝锥密度,具有超过590 MPa的机械强度和仅限制10.9%的体积膨胀。该阳极具有高容量(908.3 mAh cm-3),超快充电性(200 a g-1,完全充电/放电仅5.5 s),以及超过12,000次循环的出色可循环性,即使在- 30°C下也能保持出色的循环稳定性。与Na3V2(PO4)3阴极配对的电池在36℃下循环600次后仍保持80%以上的容量,显示出126℃(28.6 s)的显着倍率能力。我们的综合实验评估和化学力学模拟揭示了支撑阳极优越性能的机制。这一发展标志着高性能sib耐用和快速充电阳极设计的重大进步。
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来源期刊
CiteScore
24.40
自引率
6.00%
发文量
2398
审稿时长
1.6 months
期刊介绍: The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.
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