材料科学
锂(药物)
电极
导电体
离子键合
离子
锂离子电池的纳米结构
光电子学
纳米技术
电化学
复合材料
物理化学
有机化学
医学
化学
内分泌学
作者
Xiaoxue Chen,Renming Zhan,Zihe Chen,Xiancheng Wang,Shuibin Tu,Shiyu Liu,Yujie Zeng,Tiancheng Dong,Kai Cheng,Yangtao Ou,Yuchen Tan,Yongming Sun
标识
DOI:10.1002/aenm.202500242
摘要
Abstract The attainment of lithium‐ion batteries (LIBs) featuring high energy density necessitates the anode to exhibit substantial mass loading and thickness. However, this presents a formidable challenge for fast charging due to inferior Li‐ion transport capability throughout the electrode depth, resulting in diminished capacity, reduced lifespan, and potential safety hazards. Here, an alternative strategy is put forth that utilizes an electronic/ionic hybrid conductive additive as a substitution for the conventional conductive reagent. This particular additive showcases carbon black (CB) particles adorned with ultrathin red phosphorus nanolayer (≈2 nm) (CB‐P), which undergo in situ transformation into stable ultrathin lithium phosphide (Li 3 P) nanolayer‐coated CB particles during the operation of the battery. Benefiting from the significant contribution of Li + conductive enhancement, the introduction of Li 3 P enables significantly increased apparent Li + transference number and similar ionic conductivity compared to CB additive (0.67 vs 0.42, 5.2 vs 4.1 mS cm −1 ). Notably, the pouch cell with graphite anode and CB‐P additive demonstrates a high capacity filling ratio of 83.5% within 15 min (4C, relative to that at 0.5C) under a high anode loading of 14.4 mg cm −2 (4.4 mAh cm −2 at 0.5C). The full pouch cell with SiO x anode and CB‐P additive exhibits an 82.1% capacity refilling at 4C charging rate (15 min, relative to that of 0.2C). In consideration of the superior compatibility with current electrode processing, the CB‐P additive can serve as a direct replacement for traditional CB additives in existing batteries and boost the implementation of fast‐charging LIBs with high energy density.
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