贺高红

个人信息Personal Information

教授

博士生导师

硕士生导师

任职 : 精细化工全国重点实验室主任,教育部智能材料化工前沿科学中心执行主任,大连理工大学膜科学与技术研究开发中心主任

性别:女

毕业院校:中国科学院大连化物所

学位:博士

所在单位:化工学院

学科:化学工程. 膜科学与技术. 生物医学工程

联系方式:hgaohong@dlut.edu.cn

电子邮箱:hgaohong@dlut.edu.cn

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Anion exchange membranes with "rigid-side-chain" symmetric piperazinium structures for fuel cell exceeding 1.2 W cm(-2) at 60 degrees C

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论文类型:期刊论文

发表时间:2019-10-31

发表刊物:JOURNAL OF POWER SOURCES

收录刊物:EI、SCIE

卷号:438

ISSN号:0378-7753

关键字:Fuel cells; Hydroxide exchange membrane; Symmetric piperazinium; Rigid side chain; Phase separation

摘要:Developing anion exchange membranes (AEMs) having high hydroxide conductivity, swelling resistance and excellent alkaline stability is a challenge for fuel cells now. Herein, a universal and controllable approach of grafting rigid side chain is first proposed to construct connected ion transport nano-channels. A new route is also provided to prepare AEMs with stable symmetric saturated heterocyclic amomium. The rigid side chain is introduced onto poly(2,6-dimethyl-1,4-phenylene oxide) (PPO) by the Friedel-Crafts acylation with 4-fluorobenzoyl chloride and subsequent reaction between phenyl fluoride and secondary amine of 1-methylpiperazine. Then the terminal piperazinium is produced by the reaction between tertiary amine of 1-methylpiperazine and methyl iodide. Rigid branches expand free volume to construct connected ion transport nano-channels, leading to excellent conductivity (108 mS cm(-1) at 60 degrees C) that is higher than those of other reported symmetric heterocyclic amomium functionalized AEMs (33-89 mS cm(-1) at 60 degrees C). Due to the high conductivity, the H-2/O-2 cell employing this membrane achieves one of the highest peak power densities (1210 mW cm(-2) at 2600 mA cm(-2)) so far. In addition, the IEC of the membrane remains constant after testing in 1 M NaOH at 60 degrees C over 500 h.