Entrapping polyiodide by using highly N, P co-doping porous carbon framework towards high performance zinc-iodine batteries

被引:0
|
作者
Wang, Yudan [1 ,2 ]
Zhang, Xin [1 ,2 ]
Li, Xue [1 ,2 ]
Jiang, Yaru [1 ,2 ]
Shen, Tianxin [1 ,2 ]
Peng, Jinsong [1 ,2 ]
Chen, Chunxia [1 ,2 ]
Yu, Dengfeng [3 ]
Zhao, Gongyuan [1 ,2 ]
机构
[1] Northeast Forestry Univ, Coll Chem Chem Engn & Resource Utilizat, 26 Hexing Rd, Harbin 150040, Peoples R China
[2] Northeast Forestry Univ, Ctr Innovat Res Synthet Chem & Resource Utilizat, Harbin 150040, Peoples R China
[3] Tsinghua Univ, Sch Mat Sci & Engn, State Key Lab New Ceram & Fine Proc, Beijing 100084, Peoples R China
关键词
Zinc iodine battery; Heteroatoms doping; High specific capacity; Pore structure;
D O I
10.1016/j.diamond.2024.111685
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Rechargeable aqueous zinc-iodine batteries (ZIBs) with low environmental impact and abundant natural reserves have become promising electrochemical energy storage devices. However, the shuttle effect and low conductivity lead to poor electrochemical performance, hindering their practical applications. Herein, a (NH4)3PO4-activated ZIF-8-derived porous carbon (NPPC) is proposed for entrapping iodine species in ZIBs. Benefiting from its abundant porous structure and highly conductive framework, the iodine loading and electron transport of NPPC is greatly enhanced. In addition, the in-situ doping multiple heteroatoms (N, P and O) in the carbon framework can also establish chemical anchoring with iodine species and hence mitigate the shuttle effect. As a result, the ZIBs prepared by the NPPC-1.5/I2 electrode achieves an ultra-high specific capacity of 175 mAhg- 1 at 0.1 A g- 1, and a specific capacity of 95 mAh g- 1 at a high current density of 10 A g- 1. An extremely stable cycle performance of 97 % capacity retaining after 6000 cycles at 10 A g- 1 is also obtained. This study provides a new strategy for realizing aqueous ZIBs with high capacity and long cycling life.
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页数:9
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