Hydrogen substituted graphdiyne as carbon-rich flexible electrode for lithium and sodium ion batteries

被引:539
作者
He, Jianjiang [1 ,2 ]
Wang, Ning [1 ]
Cui, Zili [1 ]
Du, Huiping [1 ,2 ]
Fu, Lin [1 ,2 ]
Huang, Changshui [1 ]
Yang, Ze [1 ]
Shen, Xiangyan [1 ,2 ]
Yi, Yuanping [3 ]
Tu, Zeyi [3 ]
Li, Yuliang [3 ]
机构
[1] Chinese Acad Sci, Qingdao Inst Bioenergy & Bioproc Technol, 189 Songling Rd, Qingdao 266101, Peoples R China
[2] Univ Chinese Acad Sci, 19A Yuquan Rd, Beijing 100049, Peoples R China
[3] Chinese Acad Sci, BNLMS, CAS Key Lab Organ Solids, Inst Chem, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
HIGH-CAPACITY; ANODE MATERIAL; HIGH-POWER; STORAGE; INSERTION;
D O I
10.1038/s41467-017-01202-2
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Organic electrodes are potential alternatives to current inorganic electrode materials for lithium ion and sodium ion batteries powering portable and wearable electronics, in terms of their mechanical flexibility, function tunability and low cost. However, the low capacity, poor rate performance and rapid capacity degradation impede their practical application. Here, we concentrate on the molecular design for improved conductivity and capacity, and favorable bulk ion transport. Through an in situ cross- coupling reaction of triethynylbenzene on copper foil, the carbon-rich frame hydrogen substituted graphdiyne film is fabricated. The organic film can act as free-standing flexible electrode for both lithium ion and sodium ion batteries, and large reversible capacities of 1050 mAh g(-1) for lithium ion batteries and 650 mAh g(-1) for sodium ion batteries are achieved. The electrode also shows a superior rate and cycle performances owing to the extended pi-conjugated system, and the hierarchical pore bulk with large surface area.
引用
收藏
页数:11
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