阳极
材料科学
复合数
磷化物
煅烧
纳米颗粒
化学工程
电化学
钴
纳米技术
金属
催化作用
复合材料
电极
化学
冶金
有机化学
物理化学
工程类
作者
Kai Zhang,Mihui Park,Jing Zhang,Gi‐Hyeok Lee,Jeongyim Shin,Yong‐Mook Kang
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2017-07-25
卷期号:10 (12): 4337-4350
被引量:116
标识
DOI:10.1007/s12274-017-1649-5
摘要
Cobalt phosphide (CoP) nanoparticles which were uniformly embedded in N-doped C nanosheets (CNSs) were fabricated via the simple one-step calcination of a Co-based metal–organic framework (MOF) and red P and exhibited a high capacity, fast kinetics, and a long cycle life. This CoP/CNS composite contained small CoP particles (approximately 11.3 nm) and P–C bonds. When its electrochemical properties were evaluated by testing CoP/Na coin cells, the composite delivered a Na-storage capacity of 598 mAh·g−1 at 0.1 A·g−1 according to the total mass of the composite, which means that the capacity of pure CoP reached 831 mAh·g−1. The composite also exhibited a high rate capability and long-term cyclability (174 mAh·g−1 at 20 A·g−1 and 98.5% capacity retention after 900 cycles at 1 A·g−1), which are commonly attributed to robust P–C bonding and highly conductive CNSs. When the reaction mechanism of the CoP/CNS composite was investigated, a conversion reaction expressed as CoP + 3Na+ + 3e− ↔ Co + Na3P was observed. The outstanding Na-storage properties of the CoP/CNS composite may suggest a new strategy for developing high-performance anode materials for Na-ion batteries.
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