Surface modification of coordination polymers to enable the construction of CoP/N,P-codoped carbon nanowires towards high-performance lithium storage

被引:40
作者
Li, Huanhuan [1 ]
Zhu, Yuqiang [1 ]
Zhao, Kangjia [2 ]
Fu, Qi [2 ]
Wang, Kui [2 ]
Wang, Yaping [2 ]
Wang, Nan [1 ]
Lv, Xiaoxin [1 ]
Jiang, Haobin [1 ]
Chen, Long [1 ]
机构
[1] Jiangsu Univ, Automot Engn Res Inst, 301 Xuefu Rd, Zhenjiang 212013, Jiangsu, Peoples R China
[2] Jiangsu Univ, Sch Mat Sci & Engn, Zhenjiang 212013, Jiangsu, Peoples R China
基金
中国博士后科学基金;
关键词
Cobalt phosphide; Nitrogen and phosphorous co-doped carbon; Nanowire; Anode material; Lithium-ion battery; METAL-ORGANIC FRAMEWORKS; SODIUM-ION BATTERIES; FEP-AT-C; ANODE MATERIALS; DOPED GRAPHENE; SUPERIOR PERFORMANCE; OXYGEN REDUCTION; LI; CONVERSION; NANORODS;
D O I
10.1016/j.jcis.2020.01.037
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A one-dimensional hybrid with N,P co-doped carbon nanowires threaded CoP nanoparticles is rationally fabricated by employing surface modified coordination polymers as a precursor. Ultrasmall CoP nanoparticles are well encapsulated in N,P co-doped carbon nanowires, which can effectively buffer the volume expansion of active CoP and facilitate fast lithium-ion/electron transfer during charge/discharge processes. Moreover, N,P co-doped carbon with high defect density and graphitic-N content are obtained, which facilitates high lithium storage capacity and fast electron transfer. As a result, attractive lithium storage properties are gained by employing this unique architecture as an anode material for lithiumion batteries, including high reversible charge/discharge capacities, good rate capability, and excellent long-term cycling stability. Kinetic investigation shows that the fast lithium ion uptake/release is related to the remarkable capacitive contribution. This work may offer an effective way for design well-defined transition metal phosphide-based anodes for advanced lithium-ion batteries. (C) 2020 Elsevier Inc. All rights reserved.
引用
收藏
页码:503 / 512
页数:10
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