当前位置: X-MOL 学术Electrochim. Acta › 论文详情
Our official English website, www.x-mol.net, welcomes your feedback! (Note: you will need to create a separate account there.)
Amino acid-assisted synthesis of Fe2O3/nitrogen doped graphene hydrogels as high performance electrode material
Electrochimica Acta ( IF 5.5 ) Pub Date : 2018-07-18 , DOI: 10.1016/j.electacta.2018.07.103
Dongling Wu , Penggao Liu , Tao Wang , Xingxing Chen , Liu Yang , Dianzeng Jia

Fe2O3/nitrogen-doped graphene hydrogels are synthesized by a simple hydrothermal method using amino acids with different acidities as morphology-assisting and nitrogen-doping agents, simultaneously. The Fe2O3 show a mulberry-shape in the Fe2O3/NG-Aspartic composite, which presents a three-dimensional, loose porous network with a large specific surface area. The electrostatic and metal coordination-chelation interaction among the amino acid with different net charge, Fe3+ and graphene oxide affect the morphology, structure and final electrochemical properties of the Fe2O3/NG composites. The Fe2O3/NG-Aspartic shows a higher specific capacity, longer cycle stability and better rate capability, in comparison with the Fe2O3/NG samples prepared by using basic, neutral and non-nitrogen-doped composites. The Fe2O3/NG-Asp electrode provides high energy and power densities. The superior electrochemical performance of the Fe2O3/NG-Aspartic composite is ascribed to the battery-type capacity of iron oxide, the active sites introduced by the nitrogen-doping and the excellent proton-transfer due to the three-dimensional porous network structure of the graphene.



中文翻译:

氨基酸辅助合成Fe 2 O 3 /氮掺杂石墨烯水凝胶作为高性能电极材料

通过简单的水热法,同时使用具有不同酸度的氨基酸作为形态学辅助剂和氮掺杂剂,合成了Fe 2 O 3 /氮掺杂石墨烯水凝胶。Fe 2 O 3在Fe 2 O 3 / NG-天冬氨酸复合物中呈桑树状,呈现出具有大比表面积的三维疏松多孔网络。具有不同净电荷的氨基酸,Fe 3+和氧化石墨烯之间的静电和金属配位-螯合相互作用影响Fe 2 O 3 / NG复合材料的形貌,结构和最终的电化学性能。铁2与使用碱性,中性和非氮掺杂的复合材料制备的Fe 2 O 3 / NG样品相比,O 3 / NG-天冬氨酸具有更高的比容量,更长的循环稳定性和更好的倍率性能。Fe 2 O 3 / NG-Asp电极可提供高能量和功率密度。Fe 2 O 3 / NG-天冬氨酸复合物的优异电化学性能归因于氧化铁的电池型容量,氮掺杂引入的活性位点和三维多孔网络带来的优异的质子转移石墨烯的结构。

更新日期:2018-07-19
down
wechat
bug