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Rational design of a synthetic strategy, carburizing approach and pore-forming pattern to unlock the cycle reversibility and rate capability of micro-agglomerated LiMn0.8Fe0.2PO4 cathode materials†
Journal of Materials Chemistry A ( IF 10.7 ) Pub Date : 2018-05-05 00:00:00 , DOI: 10.1039/c8ta03418d
Yan Wang,Cheng-Yu Wu,Hao Yang,Jenq-Gong Duh

Nanometer-sized LiMn0.8Fe0.2PO4 (nano-LMFP) is one of the most suitable LiMnPO4 derived cathode materials to maximize gravimetric capacity and rate capability. However, the poor cycling performance, low volumetric energy density and safety hazards of nano-LMFP limit its large-scale commercialization. To overcome these development bottlenecks, a uniform three-dimensional interconnected conductive carbon network modified LiMn0.8Fe0.2PO4 nanoporous micro-agglomerated (micro-LMFP/C) composite was synthesized via a three-step solid-state reaction (3S) combined with three-step carburizing (3C) and two-step pore-forming (2P). The novel micro-LMFP/C composite exhibits excellent gravimetric/volumetric reversible capacities, weak electrochemical polarization and high rate capability. Even if increased to 20C, a satisfactory discharge capacity of 92.5 mA h g−1 (70.2% of the initial value at 0.1C) and an outstanding discharge plateau of 3.76 V can be observed. More importantly, for the 3S synthetic strategies, the novel 3C2P-assisted synthesis of micro-LMFP/C composites can simultaneously deliver 2.6 and 1.5 times higher volumetric capacity than that of synchronous and stepwise carburizing assisted synthesis of samples, respectively.

中文翻译:

合理设计合成策略,渗碳方法和孔形成方式,以释放微团聚的LiMn 0.8 Fe 0.2 PO 4正极材料的循环可逆性和速率能力

纳米尺寸的LiMn 0.8 Fe 0.2 PO 4(纳米LMFP)是最适合LiMnPO 4衍生的阴极材料之一,可最大程度地提高重量分析能力和倍率分析能力。然而,纳米LMFP的不良循环性能,低体积能量密度和安全隐患限制了其大规模的商业化。为了克服这些发展瓶颈,通过以下方法合成了均匀的三维互连导电碳网络改性的LiMn 0.8 Fe 0.2 PO 4纳米多孔微团聚(micro-LMFP / C)复合材料三步固相反应(3S)与三步渗碳(3C)和两步成孔(2P)相结合。新型的微型LMFP / C复合材料表现出优异的重量/体积可逆容量,弱电化学极化和高倍率容量。即使增加到20C,也可以观察到令人满意的92.5 mA hg -1的放电容量(0.1C时为初始值的70.2%)和3.76 V的出色放电平稳性。更重要的是,对于3S合成策略,新型3C2P辅助的微型LMFP / C复合材料可以同时提供比同步和逐步渗碳辅助样品合成高2.6和1.5倍的容积。
更新日期:2018-05-05
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