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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A morphology strategy to disentangle conductivity-selectivity dilemma in proton exchange membranes for vanadium flow batteries

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论文类型:期刊论文

发表时间:2018-05-01

发表刊物:PROCESS SAFETY AND ENVIRONMENTAL PROTECTION

收录刊物:SCIE、EI、CPCI-S

卷号:116

页面范围:126-136

ISSN号:0957-5820

关键字:Defect-free skin layer; Asymmetric morphology; Conductivity-selectivity dilemma; Porogen-leaching-out method; Proton exchange membrane; Vanadium flow battery

摘要:A novel integrally thin skinned asymmetric proton exchange membrane (ITSA-PEM) is proposed to disentangle the typical conductivity-selectivity dilemma in PEMs for vanadium flow batteries (VFBs). The membrane is successfully fabricated by a porogen-leaching-out method. It consists of a porous sublayer and an ultrathin skin layer, which is defect-free verified by the high H-2/N-2 separation factor of 64.9. The degree of sulfonation (DS) of PEM is reduced to extremely low (DS = 36.3%) to suppress swelling, and numerous interconnected pores are introduced to facilitate proton transfer. Low swelling ratio and defect-free skin layer lead to undetectable vanadium permeation. Meanwhile, the area resistance of ITSA-PEM is dramatically lowered to 2.1 Omega cm(2) from 5.4 Omega cm(2) of the dense PEM. Therefore a membrane with both improved proton conductivity and ion selectivity is obtained. Low DS also equips the membrane with sufficient mechanical strength and enhanced thermal stability. The VFB assembled with ITSA-PEM displays high energy efficiencies (EE: 75.6-90.2%) over a current density of 20-80 mA cm(-2), much superior to those of Nafion 211 (EE: 55.9-73.4%). It also shows favorable stability and slow capacity decay rate during cycling test over 50 cycles. (C) 2017 Published by Elsevier B.V. on behalf of Institution of Chemical Engineers.