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首页> 外文期刊>Journal of Materials Chemistry, A. Materials for energy and sustainability >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
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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

机译:合成策略的合理设计,渗碳方法和孔隙成型图案,以解锁微凝聚的LiMn0.8Fe0.2PO4阴极材料的循环可逆性和速率能力

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摘要

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.
机译:纳米尺寸的LIMN0.8FE0.2PO4(NANO-LMFP)是最合适的LIMNPO4衍生的阴极材料之一,以最大化重量容量和速率能力。然而,循环性能不良,容积能量密度低,纳米LMFP的安全危险限制了其大规模商业化。为了克服这些发展瓶颈,通过三步固态反应(3S)合成三维三维相互连接的导电碳网络改性的LiMn0.8Fe0.2PO4纳米多孔微凝聚(Micro-LMFP / C)复合物。 - 渗碳(3c)和两步孔形成(2p)。新型Micro-LMFP / C复合材料具有优异的重量/体积可逆容量,弱电化学极化和高速率能力。即使增加到20℃,也可以观察到令人满意的放电容量为92.5 mA H(-1)(0.1℃的初始值的70.2%)和3.76V的出色排放高原。更重要的是,对于3S合成策略,新型3C2P辅助合成的微LMFP / C复合材料可以同时递送比同步和逐步渗碳辅助合成样品的体积容量较高的2.6%和1.5倍。

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