Achieving Fast and Durable Lithium Storage through Amorphous FeP Nanoparticles Encapsulated in Ultrathin 3D P-Doped Porous Carbon Nanosheets

材料科学 阳极 纳米颗粒 无定形固体 磷化物 化学工程 无定形碳 锂(药物) 透射电子显微镜 纳米技术 电极 金属 化学 有机化学 物理化学 工程类 内分泌学 医学 冶金
作者
Zhiming Zheng,Hong‐Hui Wu,Haodong Liu,Qiaobao Zhang,Xin He,Sicen Yu,Victoria Petrova,Jun Feng,Robert Kostecki,Ping Liu,Dong‐Liang Peng,Meilin Liu,Ming‐Sheng Wang
出处
期刊:ACS Nano [American Chemical Society]
卷期号:14 (8): 9545-9561 被引量:318
标识
DOI:10.1021/acsnano.9b08575
摘要

Conversion-type transition-metal phosphide anode materials with high theoretical capacity usually suffer from low-rate capability and severe capacity decay, which are mainly caused by their inferior electronic conductivities and large volumetric variations together with the poor reversibility of discharge product (Li3P), impeding their practical applications. Herein, guided by density functional theory calculations, these obstacles are simultaneously mitigated by confining amorphous FeP nanoparticles into ultrathin 3D interconnected P-doped porous carbon nanosheets (denoted as FeP@CNs) via a facile approach, forming an intriguing 3D flake-CNs-like configuration. As an anode for lithium-ion batteries (LIBs), the resulting FeP@CNs electrode not only reaches a high reversible capacity (837 mA h g-1 after 300 cycles at 0.2 A g-1) and an exceptional rate capability (403 mA h g-1 at 16 A g-1) but also exhibits extraordinary durability (2500 cycles, 563 mA h g-1 at 4 A g-1, 98% capacity retention). By combining DFT calculations, in situ transmission electron microscopy, and a suite of ex situ microscopic and spectroscopic techniques, we show that the superior performances of FeP@CNs anode originate from its prominent structural and compositional merits, which render fast electron/ion-transport kinetics and abundant active sites (amorphous FeP nanoparticles and structural defects in P-doped CNs) for charge storage, promote the reversibility of conversion reactions, and buffer the volume variations while preventing pulverization/aggregation of FeP during cycling, thus enabling a high rate and highly durable lithium storage. Furthermore, a full cell composed of the prelithiated FeP@CNs anode and commercial LiFePO4 cathode exhibits impressive rate performance while maintaining superior cycling stability. This work fundamentally and experimentally presents a facile and effective structural engineering strategy for markedly improving the performance of conversion-type anodes for advanced LIBs.
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