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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Nanoscale Solid Superacid-Coupled Polybenzimidazole Membrane with High Ion Selectivity for Flow Batteries

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论文类型:期刊论文

发表时间:2021-04-04

发表刊物:ACS SUSTAINABLE CHEMISTRY & ENGINEERING

卷号:8

期号:44

页面范围:16493-16502

ISSN号:2168-0485

关键字:nanoscale solid superacid; ion selectivity; polybenzimidazole; membrane; flow battery

摘要:Nanoscale solid superacid SO42-/ZrO2/WO3 is coupled into imidazole-hydroxyl-quaternary ammonium co-functionalized polybenzimidazole (PG112) to address the trade-off effect of membrane for large-scale flow battery application. Nanoscale SO42-/ZrO2/WO3 particles with high sulfonic groups are dispersed in membrane as redox-active ion barriers and proton carriers, which mitigate the electrolyte crossover and maintain high ion conductivity. The VO2+ permeability of the prepared membrane (7.86 x 10(-)(10) cm(2) s(-1)) is significantly lower than those of PG112 (3.93 x 10(-9) cm(2) s(-1)) and Nafion 212 (7.76 x 10(-8) cm(2) s(-1)) membranes. The vanadium flow battery with this membrane exhibits a longer self-discharge duration time of 231 h compared with Nafion 212 (35 h) and PG112 (88 h) membranes. High coulombic efficiencies of 97.5-99.2% at 40-120 mA cm(-2) are obtained for the prepared membrane, which are higher than those for Nafion 212 (78.0-92.8%) and PG112 membranes (96.2-98.6%). Stable cycle performance and low retention capacity are also observed, suggesting the excellent chemical stability of the prepared membrane in vanadium flow battery operation. This work provides a prospective and applicable membrane to enhance the performance of flow battery.