Phytic Acid Assisted Fabrication of High Specific Surface Area Carbon-Wrapped Ni2P4O12 Nanoparticle Electrodes for Lithium-Ion Battery

被引:6
作者
Pang, Mingjun [1 ]
Mao, Miaomiao [1 ]
Liu, Liangbao [2 ]
Li, Ning [1 ]
Jiang, Shang [1 ]
Zhang, Ruxia [1 ]
Song, Zhaoyang [1 ]
Pang, Min [1 ]
Wang, Runwei [3 ]
Zhao, Jianguo [1 ]
机构
[1] Shanxi Datong Univ, Engn Res Ctr Coal Based Ecol Carbon Sequestrat Tec, Minist Educ, Datong 037009, Peoples R China
[2] China Acad Aerosp Aerodynam, Beijing 100074, Peoples R China
[3] Jilin Univ, Coll Chem, State Key Lab Inorgan Synth & Preparat Chem, Changchun 130012, Peoples R China
基金
中国国家自然科学基金;
关键词
Ni2P4O12; lithium-ionbatteries; phytic acid; electrochemical performance; SUPERIOR ANODE; CO; COMPOSITE;
D O I
10.1021/acssuschemeng.4c01971
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Transition metal tetrametaphosphates (M2P4O12) are a novel electrode material for lithium-ion batteries (LIBs) due to their good electrical conductivity and reversible redox behavior. In this work, carbon layer self-encapsulated Ni2P4O12 nanoparticles were prepared by facile oil bath evaporation and high temperature calcination. A detailed investigation of the synthesis mechanism was performed through controlled variables. Among the various synthesis factors, the glucose introduction generates a self-coated carbon layer; the calcination temperature can directly affect the crystalline phase formation; the product was calcined at 800 degrees equipped with the optimal lithium storage performance; the selection of organic phytic acid was correlated with the Ni2P4O12 micromorphology; and the dosage of phytic acid, while having an insignificant effect on the crystalline phase, strongly associated with lithium-ion storage. 4 mL of the phytic acid-synthesized Ni2P4O12 material showed the best lithium storage performance. On this basis, the fabricated NPO-PA-GL electrode materials were applied in LIBs, and electrochemical tests were conducted. Benefiting from the modulated electronic structure of the carbon layer, high specific surface area, and nanoparticle structure, the NPO-PA-GL electrode exhibited high-efficiency electrochemical activity. Particularly, the cell capacity amounted to 871.8 mA h g(-1) at a current density of 50 mA g(-1). After 500 constant-current charge/discharge cycles at 1 A g(-1), the capacity increased by 128.4%. This work not only indicated that NPO-PA-GL would be a prospective LIB anode material but also pointed out a new direction for the exploitation of LIB anode materials, which will lead to significant innovations in sustainable chemistry and engineering.
引用
收藏
页码:8846 / 8859
页数:14
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